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Senior Clinical Scientist- Vaccines and Immunotherapy, Cambridge



Cambridge, United States 

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Job Summary

The candidate has global scientific responsibility for a part of a clinical program. The candidate is responsible for both scientific input to clinical development strategies, acting as the primary liaison between the assigned therapeutic area and key stakeholders to ensure translation of the development plan into operational deliverables.

Responsibility for and contribution to the scientific content of clinical program documents is a key deliverable and includes study synopses and protocols, Investigator’s Brochures, clinical study reports, conference abstracts, internal and external scientific meeting presentations and peer-reviewed publications.

The Senior Clinical Scientist operates with supervision and review of the Principal Clinical Scientist, Clinical Program Director and/or Therapeutic Area Head, but is the authorized representative of the Therapeutic Area on cross-functional operational teams for the conduct of clinical research.

Some key responsibilities include:

The scientific development of individual clinical studies
Clinical oversight
Reviewing clinical data
Liaise with internal stakeholders
Manage contractual and budget requirements
Assist with planning and monitoring of timelines, resources and budgets


* MD or PhD
* 3-5 years of experience in clinical research
* Proven ability to work effectively both independently or in a team setting, and to meet set goals by managing own timelines.
* Strong research skills, knowledge of scientific analysis, data mining, and basic statistical analysis principles required.
* Experience in analyzing and presenting research results to scientific and professional audiences.
* Experience working in a cross-functional, matrix environment. Exposure to global multi-cultural teams is desirable.
* Experience with the operational aspects of clinical trials and related activities such as investigator meetings, DSMB’s, and GCP/ICH are necessary.
* Excellent communication and presentation skills required. Experience in medical/regulatory writing preferable.
* Good understanding of the drug development process, strong knowledge of ICH/GCP.
* Ability to work successfully in a matrix organization and across multiple disciplines, including clinical, regulatory, pre-clinical, product development and commercial management.
* Proven networking skills and ability to share knowledge and experience among colleagues.

If this sounds like you, send your resume/CV to g.lafebre@nonstopconsulting.com

NonStop is one of the largest and fastest-growing specialized life sciences recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Luxembourg, Switzerland, Romania, the US and the Czech Republic and we hold labor leasing licenses across Europe. Please visit our website for a full list of the niche markets we cover
Company Info
NonStop Consulting
25 Canada Square, Canary Wharf
London, United Kingdom
Phone: +44 0207 234 0550
Web Site: www.nonstopconsulting.com
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