Hobson Prior are looking for a Senior Clinical Scientist to join a world-wide pharmaceutical organisation on a permanent basis in the Netherlands. Our client specialises in developing novel vaccines to tackle pandemic threats and diseases all over the world.

Job Responsibilities:

• Accountable for the clinical oversight and medical guidance during the conduct of the study, in collaboration with the Principal Clinical Scientist and (Senior) Global Clinical Program Director.
• Reviews clinical data and contributes to the development of clinical presentations and integration of analyses into clinical documents.
• Communicates closely with the Benefit-Risk Physician to support ongoing aggregate safety data review during a given clinical study.
• Self-sufficiently review study subject level data, and present relevant issues to the medical monitor for clinical decision making, throughout the study life cycle.
• Communicate with internal stakeholders (clinical operations, data management, statistics, safety, commercial, and regulatory affairs) and investigators.
• Operations, and Pharmacovigilance functions to ensure the translation of the protocol and clinical development plans into executable operational processes.
• Lead internal or external training as required and support the medical monitor in responses to investigators and other site personnel regarding clinical and study conduct questions.
• Assure that each clinical study is globally coherent, and is consistent with the global clinical development plan, including consideration of functions beyond Clinical Development, such as Medical Affairs, Commercial and Technical Operations.
• Partakes in analysing and interpreting final data from clinical studies, and writing/editing or reviewing results in study reports, regulatory submissions, abstracts, posters, presentations, peer reviewed manuscripts, and other documents.
• Serve as a scientific reviewer for company publications and external research proposals in the areas of expertise.

Key Skills:

• Strong communication and presentation skills required.
• Experience in medical/regulatory writing preferable.
• Proven networking skills and ability to share knowledge and experience among colleagues.
• Proven ability to work effectively both independently or in a team setting, and to meet set goals by managing own timelines.
• Ability to work successfully in a matrix organization and across multiple disciplines, including clinical, regulatory, pre-clinical, product development and commercial management.

Requirements:

• Advanced degree (MD, PhD or PharmD) in life science/healthcare required.
• Proven experience within clinical research.
• Strong research skills, knowledge of scientific analysis, data mining, and basic statistical analysis principles required.
• Experience with the operational aspects of clinical trials and related activities such as investigator meetings, DSMB's, and GCP/ICH are necessary.
• Good understanding of drug development process, strong knowledge of ICH/GCP.

Apply now:

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.