Ajankohtaista

Director of FIMM Technology Centre – Institute for Molecular Medicine Finland (FIMM)

2.10.2022 | Avoimet työpaikat

https://jobs.helsinki.fi/job/Director-of-FIMM-Technology-Centre/754672602/

The Institute for Molecular Medicine Finland (FIMM) is an international research unit focusing on human genomics and personalised medicine at the Helsinki Institute of Life Science (HiLIFE) of the University of Helsinki – a leading Nordic university with a strong commitment to life science research. As part of Academic Medical Center Helsinki in Meilahti campus FIMM collaborates locally with the Faculty of Medicine, Helsinki University Hospital and National Institute for Health and Welfare. FIMM is part of the Nordic EMBL Partnership for Molecular Medicine, composed of the European Molecular Biology Laboratory (EMBL) and the centres for molecular medicine in Norway, Sweden and Denmark, and the EU-LIFE Community.

FIMM is currently seeking

Director of FIMM Technology Centre

We seek an experienced candidate to provide operational and strategic leadership at the Institute for Molecular Medicine Finland (FIMM) Technology Centre. FIMM Technology Centre consists of nine core facilities that support both local and national research communities. The total number of staff is 50 and each facility is run by a senior staff member supported by a team of technology experts. Current services include biobanking, sample preparation, genomics, transcriptomics, metabolomics, single-cell technologies, drug sensitivity screening, high-content imaging, and digital microscopy & molecular pathology. Most facilities also provide relevant data processing and bioinformatics services. All facilities are open access with the majority of users coming from Finnish universities and academic research institutions, though industry and international users are common.

The successful candidate will be responsible for leading and developing FIMM Technology Centre. This will include direct line management of a number of staff scientists leading technology teams or critical services, as well as an overall responsibility for a variety of tasks including budgets, pricing, and recruitment. The person will also support the FIMM Director in making strategic decisions on space usage and major instrument purchases, and will join a group of Research Directors at FIMM that work with the Director to define overall institutional strategy and direction.

A critical part of the role is ensuring that FIMM Technology Centre services align with the needs of FIMM research groups and the wider research community. To do this, the candidate will be able to use up to 20% of their working time on their own research with focus on method/technology development. Limited internal funds will be available to support these activities with the expectation that these will primarily be supported by securing external funding.

The candidate will join relevant internal and external decision-making groups to advocate the use of available services, and to recognise unmet technological needs of the research community. They will have a key role in the further development of life science research infrastructure programme at the University of Helsinki including the identification of potential synergies between existing core facilities, and will participate in the exchange of best practices to increase operational robustness and to minimise service overlap across campuses. The ideal candidate will have sufficient experience to lead local and/or national technology platform networks and represent FIMM and the Finnish research community in international networks.

We value candidates with strong leadership skills and vision in developing sustainable services that will serve the research community optimally. We are seeking candidates with an excellent record of accomplishments in leading research core facilities or wider infrastructures, preferably in an academic setting. In addition to a keen interest in technology development and management, particular value will be given to candidates with significant national and international contacts and familiarity with the emerging trends in technologies relevant to FIMM research grand challenges.

The working language of FIMM is English, so excellent communication skills in English are required. The salary will be commensurate with experience and qualifications based on the University salary system. The position is initially for five years, starts as soon as possible upon mutual agreement and may be renewed upon evaluation and mutual agreement. The post will include a trial period of 6 months.

Applications should include a 1-page cover letter summarising the applicant’s career and future plans and a CV including the names of three references. We also request an outline for the vision of FIMM Technology Centre development and operations (max three pages) that emphasises support for FIMM research.

Please submit your application, together with the attachments, as a single pdf file through the University of Helsinki recruitment system by clicking on the Apply button.

Application deadline is 9 October 2022 .

For further information, please visit our website at https://www.fimm.fi/en/services/technology-centre

For further information or questions related to the recruitment process, please contact FIMM Director Mark Daly fimm-director@helsinki.fi or FIMM TC Director Katja Kivinen katja.kivinen@helsinki.fi .

For technical support with the recruitment system, please contact rekrytointi@helsinki.fi .

Do you have a helsinki.fi username and a valid employment contract, a grant researcher’s contract, a visiting researcher’s or visiting professor’s contract at the University of Helsinki? Log in here to apply to our open positions.

Laboratory assistant (Virology, Vaccine development and Immunology) / Laboratorioassistentti – Tampere University Tampere, Pirkanmaa, Finland On-site

24.9.2022 | Avoimet työpaikat

https://www.linkedin.com/jobs/view/3267504834

About the job

Tampere University and Tampere University of Applied Sciences create a unique environment for multidisciplinary, inspirational and high-impact research and education. Our universities community has its competitive edges in technology, health and society. www.tuni.fi/en

Laboratory assistant position is available in the research group of Docent Minna Hankaniemi starting as agreed until the end of July, 2024. Our research group at the Faculty of Medicine and Health Technology aims to establish powerful protein-based vaccine platforms against pandemic pathogens (such as corona-, entero- and influenza viruses).

Job Description

We are looking for hard-working and enthusiastic research assistant to support our scientists in the research projects primarily involved in preclinical safety and efficacy studies of novel vaccine candidates, immunological in vitro analyses and mouse infection models as well as projects involved in development of protein-based vaccine platforms, their GMP compatible production methods and quality control.

We have previously developed experimental enterovirus vaccines with traditional and virus-like particle (VLP) based methods as well as VLP-based vaccine platform wherein any antigen can be conjugated to boost the immune responses to these antigens.

Recently, we have received funding from Business Finland, Tampere Tuberculosis Foundation and Finnish Cultural Foundation for demonstrating the proof-of-concept for the functionality of our protein-based coronavirus vaccine, strongly emphasizing the identification of the optimal route of commercialization for the developed vaccine.

Position Requirements

  • A degree in a relevant area (laboratory technician, laboratory analyst, bioanalyst, laboratory engineer, biotechnology engineer or equivalent)
  • Experience in preclinical animal studies (handling and sampling of mice, extracting primary cells, histological staining of tissue sections) and immunological analyses (e.g. serological and T-cell analyses by ELISA and FACS)
  • Experience in protein quantity, quality and purity analyses (such as SDS-PAGE, Western blot, protein concentration, dsDNA, endotoxin measurements)
  • Experience in cell biology and molecular biology techniques
  • Experience in advanced cell culture methods
  • Ability to work independently and ability to cooperate

Please be prepared to provide a proof of your merits when requested.

Our ideal candidate should have a track record in molecular cell biology, biotechnology, immunology, protein engineering, immunobiology or any other relevant field of work connected to virology, vaccine development, vaccine manufacturing or immunology. The candidate is also expected to support the laboratory in the following duties: preparation of buffers and reagents, maintenance and development of laboratory routines and techniques, ordering materials and reagents, checking invoices and maintenance of detailed records of scientific experiments.

The candidate should also be comfortable troubleshooting challenging projects with the scientists and meeting tight deadlines. Occasionally, some activities may require working outside of standard working hours. Good written and verbal communication skills in English is considered a benefit.

We offer

The position will be filled for a fixed-term period of 1 year. The salary will be based on both the job demands and the employee’s personal performance in accordance with the University Salary System. The position belongs to the category of other personnel and job demand level is 5-6, however depending on the work experience and merits of the selected person. The post starts with a 6-month trial period.

We offer a wide range of staff benefits, such as occupational health care, flexible working hours, excellent sports facilities on campus and several restaurants and cafés on campus with staff discounts. Please read more about working at Tampere University .

For further information or inquiries regarding the post, please contact Minna Hankaniemi by email minna.hankaniemi@tuni.fi .

Application deadline

The closing date for applications is Wednesday 5th of October 2022 (at 23.59 EEST / UTC +3). Applications will be evaluated as they are received.

Tampereen yliopisto ja Tampereen ammattikorkeakoulu muodostavat yhdessä Suomen toiseksi suurimman monitieteisen, innostavan ja vaikuttavan tutkimus- ja oppimisyhteisön. Korkeakouluyhteisömme osaamiskärjet ovat tekniikka, terveys ja yhteiskunta. Lue lisää: www.tuni.fi

Dosentti Minna Hankaniemen tutkimusryhmä lääketieteen ja terveysteknologian tiedekunnassa etsii laboratorioassistenttia määräaikaiseen työtehtävään. Tutkimusryhmä keskittyy pääasiassa kehittämään toisen sukupolven proteiinipohjaisia rokoteteknologioita pandeemisia taudinaiheuttajia vastaan. Laboratorioassistentin työnkuvaan kuuluu monipuolinen avustaminen tutkimustehtävissä, mm. soluviljely, rekombinantti-proteiinien analyysit, prekliiniset eläinkokeet (eri hiirimalleilla) sekä immunologiset analyysit. Laboratorioassistentin työ sisältää lisäksi laboratoriohankintojen koordinointia, tarjouspyyntöjen hoitamista ja ostolaskujen tarkistamista. Päivittäisten toimintojen kannalta olennaisista reagensseista, tarvikkeista ja materiaaleista huolehtiminen ja laboratorion siisteyden ylläpitäminen kuuluvat myös työtehtäviin.

Hakuohjeet

Lue tarkemmat tiedot tehtävästä ja hakuohjeet yllä olevasta englanninkielisestä ilmoituksesta.

Jätäthän hakemuksesi yliopiston sähköisellä hakulomakkeella (linkki löytyy tämän ilmoituksen alta). Hakuaika tehtävään päättyy 5.10.2022 klo 23.59. Hakemuksia käsitellään jo hakuaikana.

Senior Bioinformatician, Digital Medicine – Orion Corporation Turku, Southwest Finland, Finland Hybrid

24.9.2022 | Avoimet työpaikat

https://www.linkedin.com/jobs/view/3251358412

About the job

Do you have experience in bioinformatics and have a keen interest in data driven research and development? If you also possess an entrepreneurial mindset and are ready for new challenges in bioinformatics, Orion’s Digital Medicine department is looking forward to hearing from you.

Description Of Position

As the Senior Bioinformatician in the Digital Medicine department you will identify and explore multiple diverse clinical and omics databases and datasets to identify new target candidates for novel treatments in the fields of pain and oncology. You will also help with the on-going discovery and research projects in their everyday objectives and challenges. As part of our computational biology team, you will develop your own methods and pipelines, participating in the overall transformation to a more data driven research and development. You will collaborate heavily with both internal and external functions and partners, and you will routinely work together with our research biologists and projects.

The primary location of the role is in Turku, however, there is some room for alternative working arrangements.

Description Of Unit

We are an agile, entrepreneurial, and international department. Our R&D mission salutes the power of data, science, and new technologies, and aims to help the patients with life threatening illnesses. With us you’ll get to work with a diverse and flexible job description all the way from the initial discovery through to the beginning of clinical trials.

We offer

We offer you highly professional & experienced colleagues and the opportunity to show your talent and challenge yourself with interesting work in a modern multidisciplinary environment.

Generous health and welfare benefits are available, as well as corporate development and training opportunities.

Orion’s Sustainability Agenda sets the guidelines for the future and includes Patient safety as a top priority, Active work for a better environment, Care for well-being professionals, and Ethics at the core of our business.

Requirements

Ideally you are Ph.D. from a suitable field (e.g., biology, bioinformatics, computational biology), and have at least some industry relevant experience in bioinformatics. Experience of the omics principles cancer and/or pain (a common complex genetic disorder) will be a plus.

Also, extensive experience with exploratory data analysis and visualization of research data using e.g. R or Python is required.

You will need to be able to work as part of various teams, and thus good communication and interpersonal skills are needed.

Additional Information

If you are the person we are looking for, please submit your cover letter and CV via the link by 2nd October 2022.

For more information on the Senior Bioinformatician, please contact Sammeli Liikkanen, Director, Digital Medicine, tel. +358 509667466.

Approved medical examination which also includes drug testing is required prior to the employment. We will also carry out a security clearance prior to the employment for the selected person. Orion Corporation operates in more than 30 countries, where we Orionees, 3300 in total, work in all kinds of positions. Among us there are Research Scientists, Laboratory Technicians, Engineers and IT Specialists as well as people working in Production, just to mention some examples. We offer diverse and responsible jobs to our personnel in a truly multi-disciplinary work environment. We encourage people to develop their competences and offer opportunities to affect the job description and creating their own career path at Orion. We are searching for top talents who are ready to share our passion for the work that we do.

Quality Management System Compliance Department Manager – Agilent Technologies, Finland, On-site

24.9.2022 | Avoimet työpaikat

https://www.linkedin.com/jobs/view/3277165875

About the job

About AgilentJob DescriptionAgilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications and expertise. Agilent enables customers to gain the answers and insights they seek — so they can do what they do best: improve the world around us.One of our missions at Agilent is to help our customers around the world fight cancer and other life-threatening diseases. By providing our customers with the best solutions to ensure accurate and early diagnosis, we improve patient treatment and enhance survival rates.Organizational StructureAgilent has approximately 17,000 employees spread across Europe, the Americas and Asia Pacific. The global footprint includes sales offices, logistics centers, business facilities, and manufacturing sites in three major geographies. Agilent-s worldwide capabilities enable them to deliver high-quality solutions to their valued customers in 110 countries.Agilent-s footprintThere are 3 Business Units (called Groups in Agilent):

  • Agilent CrossLab Group (ACG)
  • Diagnostics – Genomics Group (DGG)
  • Life Sciences and Applied Markets Group (LSAM)

Diagnostics – Genomics Group (DGG) has 6 Divisions:

  • Nucleic Acid Solution Division (NASD)
  • Biomolecular Analysis Division (BAD)
  • Pathology Division (PT)
  • Reagent Partnership Division (RP)
  • Companion Diagnostics Division (CDx)
  • Genomics Division

Manufacturing sites are not always linked directly to each division, as some sites manufacture products that cover 2 or more divisions, e.g. Glostrup site in Denmark is manufacturing primarily for PT but it also manufactures for RP and CDx. Glostrups- sister-site is based in California, and it manufactures for CDx but also for RP and PT. The whole DGG is dedicated to in-vitro diagnostics (IVD) for oncology.Agilent values and cultureYou will be part of a company with culture based on to the values: innovation, trust, respect, collaboration, and uncompromising integrity. Added to these traits are speed, focus and accountability to meet customer needs and build a culture of performance that draws on the full range of people-s skills and aspirations.We will make sure you get all the training and development opportunities you need to become the best in your field!The positionThe position is within DGG, Pathology/RP Division. Quality organization in PT/RP in Agilent Technologies Denmark is in a process of transformation towards a strong robust function that will support the business and assure compliance at all times.In your role you will be responsible to:

  • Create clear and unifying vision for the QMS Compliance department to assure product and process compliance. Show visible leadership and foster enthusiasm, commitment and dedication to the unifying vision within the team.
  • Implement necessary compliance strategies, as well as develop and oversee compliance site programs. These programs include but are not limited to Quality Management Review (QMR), training programs, and site metrics.
  • Ensure mitigation of risk, negative regulatory exposure and/or adverse impact to the business.
  • Establish, implement, and analyze Quality metrics (KPIs) and drive improvements.
  • Manage audit preparedness to comply with authority, notify bodies, customer and internal audits.
  • Manage internal site Critical Quality Issues Notification (CQIN) programs to ensure consistent and accurate messaging. Evaluate and provide improvements to other communication tools to appropriately provide compliance information to other parts of organization and global partners.
  • Ensure implementation of current applicable regulatory requirements (In Vitro Diagnostic medical devices Regulation (IVDR) (EU) 2017/746, ISO13485, FDA CFR 21 Part 820) as well as Agilent Quality Management System
  • Translate business needs and objectives to team level, and set directions for the team accordingly

You will together with your team ensure:

  • Effectiveness of Document Management System (DMS)
  • Effectiveness of Learning Management System (LMS)
  • Trending of and follow up on: regulatory commitments (towards Notified Bodies and Health Authorities), timely product release, non-conformities, change controls, CAPAs, trainings, complaints
  • Drive continuous improvements for Quality Management System

You will have close cross-functional collaboration with among others Quality, Research – Development (R-D), Regulatory Affairs (RA) and Manufacturing.Qualifications

  • MSc. degree within Pharmacy, Medical Engineering, Molecular Biology or other similar natural sciences
  • +7 years of work experience in the medical device or pharmaceutical industry
  • +7 years supervisory experience (handling direct reports), including hiring, training, coaching and performance management activities
  • Preferably experience working with In Vitro Diagnostic and/or Medical Devices
  • Strong knowledge and understanding of standards and regulations: Regulation (EU) 2017/746, FDA CFR 21 Part 820, ISO 13485
  • Strong analytical skills with focus on finding the right solutions in compliance with the regulations.
  • High professional level in written and spoken English and Danish

Personal Skills

  • Data oriented with risk-based approach
  • LEAN mindset
  • Excellent communicating skills
  • Thrive working cross-functionally with people at all levels of the organization
  • Flexible, systematic and engaged teammate
  • Robust with a sense of urgency combined with a good sense of humor
  • Self-motivated with a high level of engagement

In addition to this we expect you to have a high drive and a proven track record of a strong leadership and communication skills, are focused on creating results (goal oriented), and are good at setting goals and direction. You have a good business understanding and are able to inspire change through clear communication, motivation, coaching, and working with other stakeholders in cross functional groups. This is a position in an international and dynamic working place with exciting challenges and opportunities.What we offer:

  • Outstanding company culture
  • Great environment to work
  • Career development opportunities
  • Company pension scheme and additional benefits.

Practical information

  • Deadline for application: 31. October 2022
  • Start: We will be interviewing on-going, and the position will be filled as soon as the right candidate has been identified
  • Salary: According to qualifications and Agilent defined salary range

Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.Travel RequiredOccasionalScheduleSchedule:Full timeShiftDayDurationNo End DateJob FunctionQuality/Regulatory

Bioinformatician – Genevia Technologies, Tampere, Pirkanmaa, Finland, On-site

24.9.2022 | Avoimet työpaikat

https://www.linkedin.com/jobs/view/3265724938

About the job

BIOINFORMATICIAN (Master’s level)

We are looking for a bioinformatician to join the Genevia Technologies team for an EU-funded project. The successful applicant will be working as a part of our bioinformatics team in implementing NGS data analysis pipelines for a variety of sequencing technologies. As a small company we are able to offer you a great deal of flexibility and influence on your work. We strive to foster development of your skills and your professional growth to the direction that you choose!

Your responsibilities include:

– Developing, testing and documenting NGS analysis pipelines

– Participation in implementing analysis workflows for technically challenging client projects

– Working independently with NGS data analysis projects and analyzing multiple sequencing data types

– Possible participation in the EU project meetings

What we offer:

– Opportunity to use commercially relevant genomics and bioinformatics technologies

– Gaining broad domain knowledge in biotechnology and life sciences generally

– Experience in commercial research and product development processes

– Working in a close collaboration with senior bioinformatics professionals

– Career advancement options to senior bioinformatics positions

– Flexible working hours

– Office in city center (Tampere, Finland)

– Competitive salary according to the EU funding scheme for early stage researchers (ESR), more information here: http://bigchem.eu/node/15

Desired background:

– Master’s degree in bioinformatics or computer science

– Programming experience with bash, R, and Python

– Parallel programming, cloud computing and workflow management software experience

– Experience in preparing scientific publications

N.B. This project is funded by the EU and the funding instrument does not allow applicants with a PhD degree (in any field), or recent employment history in Finland (max 12 months in Finland within last 3 years). This position is for fresh graduates maximum 4 years from graduation (the graduation must be max 4 years before starting date). This is a project-based employment for 7 months. You must be graduated as a master of science before starting in this position.

Work must be performed in Finland. Start date between 10/22-03/23. If you feel like you might be just the person we are looking for, please complete your information and answer a few warmup questions behind the link below by 25th September 2022.

Apply here: https://forms.gle/av6Q9PU38DtmQkiT8

Questions and additional information regarding the position is available from Klaus Breitholtz (+358 40 747 7672 / klaus.breitholtz@geneviatechnologies.com)

Multiple short-term doctoral researcher positions in the Health and Biosciences doctoral programme of the University of Oulu Graduate School – University of Oulu

24.9.2022 | Avoimet työpaikat

https://rekry.saima.fi/certiahome/open_job_view.html?id=000013960&did=5600&lang=en&jc=1&nav_from_open_jobs_view_new=true

The University of Oulu is part of the international scientific community producing new scientific knowledge and science-based solutions related to problems of the society. The University of Oulu is committed to educate future pioneers for building a more sustainable, intelligent and humane world. Creating new knowledge, taking responsibility and succeeding together are values that build a strong foundation for all our actions. We offer a working environment where individuals can cultivate their skills, do meaningful work, and develop professionally. The specialized research and service units of the University of Oulu enable extensive and diverse development and career opportunities for experts in various fields. Doctoral researchers in the University of Oulu are part of an international, multidisciplinary scientific community. Doctoral training is coordinated by the University of Oulu Graduate School (UniOGS).

We are now looking motivated candidates for

Multiple short-term doctoral researcher positions

in the Health and Biosciences doctoral programme (HBS-DP) of the University of Oulu Graduate School (UniOGS).

HBS-DP gathers clinical medicine, biomedicine, biochemistry, molecular medicine, dentistry, health sciences and medical technology under the umbrella of a multidisciplinary training programme.

In the current call, there are multiple full-time short-term positions (3-6 months) and multiple full-time one year positions available in HBS-DP for 2023 (starting at the earliest on 1.1.2023 and ending the latest on 31.12.2023).

Please note that you can apply for either a one year or a short-term (3-6 months) position, but not both.

Eligibility and Requirements

As an eligible candidate, you have a Master’s degree or an equivalent degree in a field relevant to the applied field. The major subject of the doctoral researcher is expected to be in the Doctoral Degree Programme of Medicine, Biochemistry and Molecular Medicine, Health Sciences or Dentistry. The degree must have been completed before the selection with at least good grades. You must meet all the requirements to receive doctoral study rights as defined in: https://www.oulu.fi/en/research/graduate-school/admissions.

– In the short-term positions, the priority will be given to doctoral researchers working as a professional in the healthcare with a degree of Licentiate of Medicine, Licentiate of Dentistry or Master of Health Sciences.

– In the one year positions, priority will be given to such doctoral researchers whose supervisor’s research group is not receiving strategic funding (via focus institutes, emerging projects, doctoral programmes etc.) related to doctoral training from the University of Oulu during the funding period 2023. In the one year positions, any applicant who has received doctoral study rights on or earlier than 31.12.2019 need to explain why they should still be considered as eligible applicants and to assure the motivation for graduating during one year.

Prior to submitting, applicants are expected to find a prospective main supervisor in an eligible research unit. Applicants are advised to seek potential supervisors in the faculty web pages (https://www.oulu.fi/en/university/faculties-and-units). The proposed main supervisor must clearly be identified in the application form (full name, title, position, faculty and research unit at the University of Oulu). A letter from the proposed supervisor willing to commit for supervision must be attached into the applicant’s set of documents (see below).

Unless explicitly stated otherwise, the commitment letter does not bind the proposed supervisor to any commitment, if the applicant is not selected into the doctoral researcher position applied here and for which the letter of support was provided.

Salary and key terms

The salary will be initially set on level 2, and later on levels 2 – 4 of the national salary scale for the teaching and research staff of Finnish universities. In addition, a supplementary remuneration is given for personal achievement and performance (max. 50 %). In practice, the salary is roughly 2200 – 2700 € per month for an early stage researcher, depending on the appointee’s qualifications and progress of the doctoral thesis.

The positions are filled earliest in the beginning of 2023 and ending the latest at December 31, 2023. A trial period is applied to these positions with maximum length being half of the employment period.

How to apply

Submit your application and attachments in English (with exceptions for Certificates/Diplomas) through the online system by 16th of October, 2022 (23:59 Finnish local time). Please include the following attachments as five separate pdf files (please note that the online system has a maximum size limit for attachments): 

  1. CV: Including a list of all peer-reviewed scientific publications with full reference details following the guidelines of the Finnish Advisory Board on Research Integrity: http://www.tenk.fi/en/template-researchers-curriculum-vitae
  2. Motivation letter: Describing prior knowledge, research interests and career plan (max 1 page).
  3. Certificates/Diplomas: Scanned electronic copies of diplomas and transcripts of the records of relevant previous degrees. If the original documents are not in Finnish, Swedish or English, each document must be accompanied by an official certified translation into Finnish or English.
  4. Research plan approved by the supervisor: Please follow the structure given in the guidelines of the Academy of Finland (https://www.aka.fi/en/research-funding/apply-for-funding/how-to-apply-for-funding/az-index-of-application-guidelines2/research-plan-structure/2020/porst-doctoral-clinical/) However, for the current purpose, the texts under the given section headings need not cover all bullet points in the guidelines, and the maximum length of the (draft) plan’s body of text must not exceed 3 pages with 10-12 point font size and with at least 1,5 cm margins. A fourth page can be used for the list of references only. Thus, the max total length of the plan including the references is 4 pages. Exceeding the page limit will either result in disqualification or removal of the extra pages from the document.
  5. Letter of provisional commitment from the supervisor (the pre-formulated form that must be used):In this document the eligible supervisor (either a professor or a docent level researcher who is employed by the University of Oulu) states his/her willingness to act as the supervisor for the applicant. Commitment letter must include the provisional supervisor’s assurance that the research unit director is aware of and committed to the financial obligations related to these positions. The University will cover only part of the costs related to this position and the unit will cover the rest. Typically, 20-35% of the salary and sidecosts remain to be covered by research unit. All other other costs are to be covered by research unit.

Applications received after the deadline, incomplete applications, and/or applications with attachments that exceed the specified limits, will not be considered.

Application and evaluation process

Evaluation and ranking of the applications will take place in multiple stages. First, ineligible or incomplete applications are rejected. Second, eligible and complete applications are evaluated and ranked by the evaluation panel. Third, applications with highest scores from the second round will be further evaluated and ranked by the corresponding Doctoral Training Committee. All applicants will be informed of the selection by e-mail.

Further information

About eligibility and degree requirements, see the Graduate School website:

https://www.oulu.fi/en/research/graduate-school

About the evaluation process: HBS-DP coordinator Mirja Peltola (firstname.lastname@oulu.fi).

Lead Clinical Research Associate – Barrington James, Finland, Remote

24.9.2022 | Avoimet työpaikat

https://www.linkedin.com/jobs/view/3265512120

About the job

LEAD CLINICAL RESEARCH ASSOCIATE – Finland – PERMANENT

As a Lead Clinical Research Associate (CRA), you will have the fantastic opportunity to join one of our CRO clients. This company are a global mid-sized CRO that strives to push boundaries by innovating and inventing. They are executing a high amount of studies globally and due to some late success with one of their Haematology Biotech clients they are looking for an experienced monitor.

As a Lead Clinical Research Associate, a typical day might include the following:

• Managing investigative site activities for multiple protocols / indications and providing ongoing updates of site status to the Study Manager / sponsor.

• Creating and implementing subject enrolment strategies for assigned investigative sites.

• Conducting study site visits (pre-study, initiation, monitoring, and close-out) and completing site visit deliverables within given timelines in the Monitoring Plan.

• Ensuring proper storage, dispensation, and accountability of all investigational product(s) and trial-related material.

• Marinating tracking records for assigned sites including tracking of subject status, subject case report form (CRF) retrieval / source document review (SCV), regulatory documents, and investigational product.

• Participating in development of CRFs and other study related documents (source documents, subject worksheets, Monitoring Plan, etc).

This role might be for you if:

  • You have a life Science Degree
  • You have 1+ years independent monitoring
  • Are willing to travel required
  • Have a full driving licence
  • Are fluent in English speaking, reading & writing

Benefits Include:

  • Competitive salary
  • Sponsor-dedicated positions
  • Clear progression routes
  • Car allowance

GET IN TOUCH TO KNOW MORE

By uploading your CV it will be sent to Ish Rathor at Barrington James. Ish is a Specialist Clinical Operations/Development Recruiter with a strong background in recruitment and the life science field. Ish will discuss the opportunity in detail with you, facilitate your application and will manage the process acting as a link between the company and yourself. He will assist in all elements of the process, facilitate the offer process, keep in contact throughout your notice period and even catch up with you during your first week in your new role.

E: Irathor@barringtonjames.com

T: +441293 776644

Researcher (RNA biochemistry) / Tutkija (RNA-biokemia) – Tampereen yliopisto 

24.9.2022 | Avoimet työpaikat

https://tuni.rekrytointi.com/paikat/?o=A_RJ&jgid=1&jid=1610

Tampere University and Tampere University of Applied Sciences create a unique environment for multidisciplinary, inspirational and high-impact research and education. Our universities community has its competitive edges in technology, health and society. www.tuni.fi/en 

We are seeking a highly motivated candidate to join us as a researcher to support a project where we study RNA regulatory mechanisms involved in platelet biogenesis. The position is located in the Functional RNAomics laboratory at the Faculty of Medicine and Health Technology, Tampere University.

The Functional RNAomics laboratory studies gene regulation via RNA processing. By determining how RNA regulation is orchestrated in different cell types, we aim to crack the cellular RNA code and gain critical insights into how aberrations in the RNA machinery result in genetic disorders and cancer. RNA is emerging as a powerful and easily adaptable therapeutic molecule as exemplified by the rapid development of effective mRNA vaccines but a detailed knowledge of RNA regulation in cells is a prerequisite to realise the full potential of RNA-based therapeutic and diagnostic development. 

Job description

The researcher is responsible for versatile cell and molecular laboratory work including cell culture and platelet isolation, cell characterization using flow cytometry and imaging techniques, basic molecular biology, sample preparation for short-read and long-read RNA sequencing, and various RNA biochemistry methods. 

Requirements

The position is intended for a biologist or a biochemist with previous experience in cell and molecular biology. We expect you to have at least a M.Sc. level degree in biochemistry, genetics, molecular biology, or a related subject area. We also expect a competence to pursue independent scientific work. You should be familiar with cell and molecular biology techniques. You should be able to communicate with experimental and computational biologists as a member of a multidisciplinary team and be fluent in spoken and written English. We appreciate experience of studying or working abroad and contacts to international research community. We are looking for versatile and independent researchers with experience in the closely related area of the positions. It is expected that you will be able to contribute to the supervision of students. Please be prepared to provide a proof of your merits when requested.

Tampere University is a unique, multidisciplinary and boldly forward-looking, evolving community. Our values are equity, openness, diversity, responsibility, courage, critical thinking, erudition bildung, and learner-centredness. We hope that you can embrace these values and promote them in your work.

We offer

The position will be filled for a fixed-term period of 2 year in the first instance. The starting date is mutually agreed. A trial period of six months applies to all our new employees.

The salary will be based on both the job requirements and the employee’s qualifications and personal performance in accordance with the Finnish University Salary System. The position of a researcher is placed on the job demands level 2-4 (teaching and research staff).

We offer a wide range of staff benefits, such as occupational health care, flexible working hours, excellent sports facilities on campus and several restaurants and cafés on campus with staff discounts. Please read more about working at Tampere University.

We offer a world-class research environment in an internationally recognized research group. We have strong collaborative networks and offer great opportunities for researchers to develop their careers in an international setting.

How to apply

Please submit your application through our online recruitment system. The closing date for applications is 14th of October 2022 (at 23.59 EET /UTC+3). Please write your application and all accompanying documents in English and attach them in PDF format.

Applications should include the following documents:

  • Curriculum Vitae according to TENK guidelines
  • List of publications according to Academy of Finland guidelines
  • Contact information for two referees
  • Motivation letter (1-2 pages) 
  • Description of your research focus, qualifications, previous research fields and main research achievements (1-2 pages)

For more information, please contact:

Associate Professor, Group Leader Minni Änkö, minna-liisa.anko(at)tuni.fi

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Tampereen yliopisto ja Tampereen ammattikorkeakoulu muodostavat yhdessä Suomen toiseksi suurimman monitieteisen, innostavan ja vaikuttavan tutkimus- ja oppimisyhteisön. Korkeakouluyhteisömme osaamiskärjet ovat tekniikka, terveys ja yhteiskunta. Lue lisää: www.tuni.fi

Functional RNAomics -tutkimusryhmä Tampereen yliopiston Lääketieteen ja terveysteknologian tiedekunnassa tutkii RNA-välitteistä geenien säätelyä. Tutkimuksemme tavoitteena on selvittää, miten RNA-tason säätely toimii eri solutyypeissä. Tarkoituksenamme on ‘murtaa solujen RNA-koodi’ ja siten ymmärtää, mikä RNA-säätelyn rooli on geneettisten sairauksien ja syövän synnyssä. RNA on osoittautunut monimuotoiseksi molekyyliksi, jota voidaan soveltaa erilaisten sairauksien hoidossa tai ehkäisyssä, esimerkkinä hiljattain kehitetyt RNA-rokotteet. Jotta RNA:ta voidaan turvallisesti hyödyntää diagnostiikassa ja hoitomuotona, meidän täytyy kuitenkin ensin selvittää, kuinka RNA-säätely toimii solutasolla. 

Tehtävänkuvaus

Tutkijan tehtäviin kuuluu muun muassa soluviljely ja RNA-biokemian menetelmät, näytteiden valmistus RNA-sekvenointiin sekä muut molekyylibiologian menetelmät. Tutkimusryhmän työkieli on englanti, joten englannin kielen taito on välttämätön.

Hakuohjeet

Lue tarkemmat tiedot tehtävästä ja hakuohjeet yllä olevasta englannin kielisestä ilmoituksesta.

Jätäthän hakemuksesi yliopiston sähköisellä hakulomakkeella (linkki löytyy tämän ilmoituksen alta).

Hakuaika tehtävään päättyy 14.10.2022 klo 23.59.

Application period starts: 2022-09-23 08:00Application period ends: 2022-10-14 23:59

Team Lead, (Cancer Cell Signaling), Oncology Research, R&D – Orion Oyj, Turku

3.9.2022 | Avoimet työpaikat

https://www.linkedin.com/jobs/view/3227545781

About the job

Orion seeks an innovative and highly motivated Scientist to lead the Cancer Cell Signaling team in Oncology Research unit in Turku.

Description Of Role

As the Team Lead you will bring your expertise in cancer biology to identify, validate, and mechanistically characterize novel oncology targets with the goal of developing life changing therapies. The focus of the team is to identify novel cancer vulnerabilities, with emphasis on cancer cell signaling and metabolism.

You will lead a team that uses a variety of genetic, biochemical, and cell biological techniques for target identification and building of the underlying mechanistic link to the disease.

Main responsibilities for this position include the following:

  • Lead a team of PhD and non-PhD level scientists with the primary focus on conducting laboratory studies from target idea to drug candidate selection
  • Develop and execute efficient strategies for target identification, prioritization, and validation
  • Lead and execute set up of relevant assays and models for in vitro and in vivo screening and efficacy studies related to research projects
  • Develop action plans, strategies, and go/no go criteria at each stage of drug discovery process
  • Serve as a leader in the Oncology Research and interact with scientific leadership within Orion to exchange data and ideas
  • Communicate project deliverables to the leaders across the oncology therapeutic area and other management groups when necessary
  • Interact with internal experts, external experts, academic groups, and CROs to establish collaborations and projects

You will be based in Turku, Finland, and report to the Director of Oncology Research.

Description Of Unit

In R&D, we offer diverse and responsible jobs to our personnel in a truly multi-disciplinary work environment. We do research in two therapy areas, Oncology and Pain. Our goal is to develop new life-changing therapies to build well-being of patients globally. Orion scientists have a long and strong history of discovering and developing innovative orally delivered small molecule drugs. Today we are also utilizing biological modalities to target the disease relevant mechanisms most efficiently and to tackle drug targets that cannot be addressed with small molecules.

Cancer Cell Signaling team is one of four research teams in Oncology Research, which together build the R&D Oncology portfolio and Oncology strategy in close collaboration with business and all R&D global functions.

We offer

  • Opportunity to work with a dynamic team of in vitro and in vivo scientists and assistants building up Oncology Research at Orion
  • A highly interesting R&D pipeline and enthusiastic working environment with opportunities to use your own strengths to build your competence and career
  • Exciting opportunity to innovate and have an impact on the future therapies for patients.

Appreciation of colleagues and continuous development are part of our core values. The culture of Orion R&D is informal, and we enjoy working together.

We are passionate about the patient welfare and serve as The Voice of Science and the Patient. Join us – together we build well-being and do work that we are proud of!

Requirements

To succeed in this Team Lead position, you have the following education and professional experience:

  • A PhD with > 6 years of post-doctoral experience in oncology research
  • Track record and strong background in cell biology, biochemistry, and oncology research
  • Deep understanding on the mechanisms that drive cancer growth and experience in using genomic data mining techniques
  • Expertise in in vitro and in vivo cancer models
  • Experience as a scientific leader/supervisor and team player with excellent organizational skills
  • Industry or biotechnology experience is an advantage but not required
  • Excellent oral and written communication skills

Candidates with a deep understanding on the mechanisms that drive cancer growth and with experience in using genomic data mining techniques to study pathways involved in cancer are encouraged to apply.

Additional Information

Are you ready to challenge yourself and join Orion’s R&D? Please apply and submit your CV at the latest on September 11th, 2022.

For more information on the Team Lead, Cancer Cell Signaling position, please contact Director of Oncology Research, Anu Moilanen +358 509667827 on August 25 at 12:30-13:30 EEST or August 29 at 16:00 EEST.

Approved medical examination which also includes drug testing is required prior to the employment. We will also carry out a security clearance prior to the employment for the selected person. Orion Corporation operates in more than 30 countries, where we Orionees, 3300 in total, work in all kinds of positions. Among us there are Research Scientists, Laboratory Technicians, Engineers and IT Specialists as well as people working in Production, just to mention some examples. We offer diverse and responsible jobs to our personnel in a truly multi-disciplinary work environment. We encourage people to develop their competences and offer opportunities to affect the job description and creating their own career path at Orion. We are searching for top talents who are ready to share our passion for the work that we do.