Senior Clinical Project Manager – Permanent – Pharmaceutical Company – CHF140,000–CHF170,000 (Depending on experience) – Office-Based RBW Consulting are excited to announce an opportunity on behalf of one of our close clients. This company are a mid-sized Pharmaceutical that produces modern and affordable treatments within haematology and immunotherapies. This admired sponsor has a rich history of innovation and stability; colleagues here always have the room for personal and professional development. They are proud to work with bright young talent as well as seasoned professionals in the industry. With a mixture of short communication lines and ample resources, this role will give you the flexibility and support necessary to perform the way you want to.
The Senior Clinical Project Manager will help drive forward interest in phase I-III of development. The CPM will act as a matrix leader and will be accountable for the timely execution of specific tasks within their assigned projects. The ideal candidate will enjoy a hands-on approach to their sites and will have great experience managing CROs to get the most out of their sites.
This is a great opportunity for someone who wants to showcase their project management experience and take full ownership for the success of their assigned trials.
Responsibilities Planning, implementation and evaluation of global clinical Phase 1-4 GCP studies
Directing activities of team members to ensure compliance with protocols and overall clinical objectives. Providing input to overall clinical development programs with coagulation and critical care products and lead the development of study protocols
Evaluate, analyse and interpret clinical data. Preparing study reports, CTDs, summary reports, expert statements, etc. for Competent Authorities
Keeping track of study budgets, involvement in vendor oversight
Interacting with Independent Data Monitoring and Steering Committees (install, update, present results, etc.)
Representing the company at meetings with Competent Authorities
Contributing to publications and prepare abstracts, posters and/or presentations for national and international congresses
Review scientific literature, participate in continuing education activities or attend conferences and seminars to maintain/keep up to date current knowledge of all aspects regarding clinical studies
Requirements 8+ years of CPM experience in a pharmaceutical or biotechnology company
Life science related degree or equivalent
To apply If you would like to discuss this vacancy further or to discuss your career options in confidence, please telephone on +44(0)1293 36092. Please click “apply” or contact Harry Henson for any further information.
#J-18808-Ljbffr