Current jobs related to Clinical Affairs Analyst - Cambridge, Cambridgeshire - JR United Kingdom

  • Clinical Affairs Analyst

    2 weeks ago

    Cambridge, Cambridgeshire, United Kingdom Meet Life Sciences Full time

    I'm currently collaborating with a company at the forefront of clinical research and diagnostics, and they're looking for a Clinical Affairs Analyst to join their team.This is an exciting opportunity to play an integral role in the design, execution, and reporting of clinical trials, ensuring that products are safe, effective, and globally available. You'll...

  • Clinical Affairs Analyst

    3 days ago

    Cambridge, Cambridgeshire, United Kingdom Meet Life Sciences Full time

    I'm currently collaborating with a company at the forefront of clinical research and diagnostics, and they're looking for a Clinical Affairs Analyst to join their team.This is an exciting opportunity to play an integral role in the design, execution, and reporting of clinical trials, ensuring that products are safe, effective, and globally available. You'll...

  • Associate Director, Regulatory Affairs

    1 week ago

    Cambridge, Cambridgeshire, United Kingdom CK Group- Science, Clinical and Technical Full time

    CK Group are working with a very well backed biotechnology company, with a strong pipeline who are looking for an Associate Director, Regulatory Affairs, for a six-month contract. The role will be in support of their expanding Oncology portfolio; extensive Oncology experience is an absolute must, radiopharmaceuticals experience would be highly advantageous....

  • Associate Director, Regulatory Affairs

    12 hours ago

    Cambridge, Cambridgeshire, United Kingdom CK Group- Science, Clinical and Technical Full time

    CK Group are working with a very well backed biotechnology company, with a strong pipeline who are looking for an Associate Director, Regulatory Affairs, for a six-month contract. The role will be in support of their expanding Oncology portfolio; extensive Oncology experience is an absolute must, radiopharmaceuticals experience would be highly advantageous....

  • Regulatory Affairs Specialist

    2 weeks ago

    Cambridge, Cambridgeshire, United Kingdom OGT Full time

    OGT is a leading global provider of clinical and diagnostic genomic solutions. We believe in creating products and partnerships that enable clinicians to deliver personalised healthcare to patients and that empower clinical researchers to develop the next generation of precision medicines.An opportunity has arisen in our Cambridge based Regulatory and...

  • Senior Director, Regulatory Affairs

    1 week ago

    Cambridge, Cambridgeshire, United Kingdom TN United Kingdom Full time

    Social network you want to login/join with:Senior Director, Regulatory Affairs, Cambridgecol-narrow-leftClient:Cpl Life SciencesLocation:Cambridge, United KingdomJob Category:Other-EU work permit required:Yescol-narrow-rightJob Reference:b3f9edc343f8Job Views:8Posted:26.04.2025Expiry Date:10.06.2025col-wideJob Description:OverviewJob Title: Senior Director,...

  • Senior Director, Regulatory Affairs

    1 day ago

    Cambridge, Cambridgeshire, United Kingdom TN United Kingdom Full time

    Social network you want to login/join with:Senior Director, Regulatory Affairs, Cambridgecol-narrow-leftClient:Cpl Life SciencesLocation:Cambridge, United KingdomJob Category:Other-EU work permit required:Yescol-narrow-rightJob Reference:b3f9edc343f8Job Views:8Posted:26.04.2025Expiry Date:10.06.2025col-wideJob Description:OverviewJob Title: Senior Director,...

  • Regulatory Affairs Specialist

    2 weeks ago

    Cambridge, Cambridgeshire, United Kingdom JR United Kingdom Full time

    Social network you want to login/join with:Regulatory Affairs Specialist, CambridgeClient:Cure TalentLocation:CambridgeJob Category:OtherEU work permit required:YesJob Views:1Posted:30.03.2025Expiry Date:14.05.2025Job Description:Cure Talent are delighted to be partnered with an exciting Diagnostics company, specialising in Gastrointestinal Cancer, who, due...

  • Regulatory Affairs Specialist

    12 hours ago

    Cambridge, Cambridgeshire, United Kingdom JR United Kingdom Full time

    Social network you want to login/join with:Regulatory Affairs Specialist, CambridgeClient:Cure TalentLocation:CambridgeJob Category:OtherEU work permit required:YesJob Views:1Posted:30.03.2025Expiry Date:14.05.2025Job Description:Cure Talent are delighted to be partnered with an exciting Diagnostics company, specialising in Gastrointestinal Cancer, who, due...

  • Senior Director, Regulatory Affairs

    7 days ago

    Cambridge, Cambridgeshire, United Kingdom Cpl Life Sciences Full time

    Overview Job Title: Senior Director, Regulatory Affairs Job Type: Full-time, permanent position Location: Cambridge, UK – Hybrid Remuneration: £130,000 + Benefits Cpl Life Sciences is collaborating with a prestigious global drug development consultancy business that specialises in supporting pharma, biotechs, spin-outs, and academic...

Clinical Affairs Analyst

2 weeks ago

Cambridge, Cambridgeshire, United Kingdom JR United Kingdom Full time

Social network you want to login/join with:

Clinical Affairs Analyst - Cambridge, cambridgeClient:

Meet Life Sciences

Location:

Cambridge

Job Category:

Other

EU work permit required:

Yes

Job Views:

7

Posted:

18.04.2025

Expiry Date:

02.06.2025

Job Description:

I'm currently collaborating with a company at the forefront of clinical research and diagnostics, and they're looking for a Clinical Affairs Analyst to join their team.

This is an exciting opportunity to play an integral role in the design, execution, and reporting of clinical trials, ensuring that products are safe, effective, and globally available. You'll be contributing to various tasks that ensure the smooth management and execution of trials and submissions, with the added responsibility of managing two direct reports.

What you'll be doing:

  1. Participating in the design and reporting of clinical trials, either directly or via Contract Research Organisations (CROs)
  2. Executing trial protocols and ensuring their timely completion
  3. Collating trial data using in-house or external specimens (e.g., haematological specimens)
  4. Processing and accurately recording biological samples and cell lines
  5. Conducting laboratory activities such as biological sample culturing, FISH setup, analysis, and troubleshooting
  6. Assisting with study monitoring and coordinating with external clinical sites to provide required clinical data
  7. Contributing to the overall analytical and practical workload

What we're looking for:

  1. A background in a science-related field (MSc or equivalent preferred)
  2. Experience working in a laboratory setting (critical for this role)
  3. Proven experience in clinical trial design and operational insights
  4. Strong problem-solving skills with the ability to troubleshoot technical laboratory issues
  5. Familiarity with GLP environments and exceptional attention to detail
  6. Strong organisational skills with the ability to manage workloads under tight deadlines
  7. Willingness to travel (10% of the time) to visit clinical labs internationally and within the UK
  8. Knowledge of cytogenetic processing methods and FISH analysis is desirable

In return, you'll receive:

  1. 10% non-contributory pension scheme
  2. Group income protection & life assurance

If you're looking for a hands-on, lab-based role where you can make a real impact in genetics research, this is an excellent opportunity to advance your career.

If you're interested or would like to learn more, feel free to reach out

#J-18808-Ljbffr