- Senior Regulatory Program Manager Oncology
The Program Manager position will be responsible for regional (EU, ROW) regulatory strategic and operational management of a project, , or a portfolio of projects
Primary Responsibilities and Accountabilities
Is responsible for and leads the development and implementation of regional regulatory strategies on projects
Gives regional strategic regulatory input to the RAFT and Project Teams for lifecycle management of products
Analyzes regulatory environment for impact on projec ...
- Senior Program Director- Biologics
We are currently searching for an experienced program (project manager) to lead the development for a leading biological product. The role will be managing all strategic and operational aspects involved in the drug development cycle working closely with Regulatory, Clinical, R&D and commercial and reports closely to the CEO and the VP for program management.
- Director, Regulatory Affairs, Biologics
Director, Regulatory Affairs, Biologics, Fast Growing Start-up, Program Lead for Development Products
- Regulatory Affairs Manager
Skills Alliance is currently retained to support the growth of a pre-clinical biopharmaceutical company as it builds its immuno-oncology team.The organization is looking to...
- Senior Regulatory Affairs Manager (Associate Director Level) North Carolina - USA
An Excellent opportunity have arisen to work in one of the most exciting areas of modern medicine within this innovative pharmaceutical company within the US - North Carolina - OFFICE based in the RTP - PERMANENT postion.
- Contract Clinical Study Manager
Contract Clinical Study Manager, UxbridgeJOB SUMMARYA Contract (Freelance) Clinical Study Manager required by Global Biotechnology Company based in the Uxbridge area. In this exciting role, working with the Clinical Program Manager, you will coordinate and supervise all aspects of assigned clinical studies in the area of Infectious Disease. I will serve as the primary point of contract for CROs. ...
- Regulatory Project Manager
Prepare and deliver regulatory operational plans for allocated projects/products. Contribute to solutions to regulatory issues. Project manage quality regulatory submissions to agreed project targets. Provide operational regulatory input and guidance in cross-functional teams. Work flexibly within and across Therapeutic Areas to provide broad regulatory support to ensure the delivery of product team and business objectives.
- Clinical Programme Manager (Oncology)
Key People are recruiting for an office based Clinical Programme Mananger for a global pharmaceutical company in France
- Senior Quality Assurance Manager (QA), London
Responsible for Implementation and Maintenance of the Quality Assurance and Training Program for UBC Europe as related to Clinical/Post Marketing programs as well as supporting Pharmacovigilance.
- **Pharmacovigilance Quality Assurance Manager - Basel, Switzerland**
A well known and successful Global Biopharmaceutical company is seeking a PV Quality Assurance Manager for a brand new opportunity based in Basel. The company have a fantastic reputation in the market, and have been successfully growing their teams throughout the year. The ideal candidate for this position will have a PV background, Audit experience and exposure to both pre and post marketing Pharmacovigilance. As well as a strong salary, the company also offer excellent growth potential.