(Senior) Clinical Project Manager - Freelance - Switzerland - 12 months con

1 post / 0 new
Job Publisher
Job Publisher's picture
(Senior) Clinical Project Manager - Freelance - Switzerland - 12 months con

Job Summary:
(Senior) Clinical Project Manager - Freelance - Switzerland - 12 months contract A new opportunity has arisen to work for a top global pharmaceutical company with an enviable product pipeline. The opportunity is suitable for candidates with an clinical trial management background and extensive exposure to the scientific aspects of clinical trial design and development. The position will be an exceptional opportunity to work in large team
 
Requirements:
 
(Senior) Clinical Project Manager - Freelance - Switzerland - 12 months contract


Company and Role Summary
A new opportunity has arisen to work for a top global pharmaceutical company with an enviable product pipeline. The opportunity is suitable for candidates with an clinical trial management background and extensive exposure to the scientific aspects of clinical trial design and development. The position will be an exceptional opportunity to work in large team where you will be able to develop skills difficult to experience in alternative companies. This opportunity is on a freelance basis with a highly competitive daily rate. Candidates with PhD or MD qualifications are highly desirable.
 
Role Summary
Phase II - IV study and program management for international clinical trials.
 
Main Duties and Responsibilities
*Support Senior Clinical Project management in ensuring all trial deliverables are met according to timelines, budget, SOPs and quality standards. Assist with program level activities.
*Develop of protocol and related documents; development study and outsourcing plans and training guidelines. Scientifically review clinical data and assist with analysis and publishing of study data. Ensure trial data is accurate in all databases
*Manage Contract Research Organizations (CROs) and ensure study is run to timelines and budget. Acts as point of contact for study SOPs and patient eligibility. Implement best practices.
*Work closely with Clinical Operations and other relevant departments and when required Advisory boards.


Education and Skills
Advanced degree i.e PhD. MD or equivalent and exposure international clinical research environments
or
BSc or equivalent in life sciences and guideline level of 2 years experience in clinical research.
Fluent English
Working knowledge of ICH/GCP clinical trial design and study budgets
 
If this role is of interest please contact Ed Bezer or Holly Morgan for a confidential discussion. +41 417232534 or +44 2078120676 or eval(unescape('%64%6f%63%75%6d%65%6e%74%2e%77%72%69%74%65%28%27%3c%61%20%68%72%65%66%3d%22%6d%61%69%6c%74%6f%3a%68%6f%6c%6c%79%2e%6d%6f%72%67%61%6e%40%63%6c%69%6e%69%63%61%6c%70%72%6f%66%65%73%73%69%6f%6e%61%6c%73%2e%65%75%22%3e%68%6f%6c%6c%79%2e%6d%6f%72%67%61%6e%40%63%6c%69%6e%69%63%61%6c%70%72%6f%66%65%73%73%69%6f%6e%61%6c%73%2e%65%75%3c%2f%61%3e%27%29%3b'))

Reference