Upvote
Downvote
Sr. Clinical Scientist - BB
Share Job
- Suggest Revision
Full-time
- Must be able to start ASAP Paid parking is required on-site Hybrid, a minimum of 2 days onsite (with flexibility to adjust due to business needs, required meetings etc.)
- This role is key to help the medical supervision of clinical studies by Clinical Research Directors (CRD) and to ensure scientific management of clinical studies to be performed by the Clinical & Sciences Operations Platform (CSO) and Development Units in Client R&D.
- The applicant must be familiar with all medical and operational aspects related to the conduct of late-stage clinical trials.
- Under the guidance of the CRD he/she collaborates with the Coding specialist, Biostatisticians, Data Managers, Global and Regional Study Managers, Feasibility Managers, Pharmacovigilance representative, Medical Writer (e.g. planning and review of narratives) on high quality medical review, as needed.
- He/she supports the CRD to ensure appropriate documentation and consistency of the data and investigations of safety cases with the Clinical Trial Team (Monitoring Teams) or Pharmacovigilance.
Active Job
Updated 3 days agoSimilar Job
Relevance
Active