Description
Clinical Project Manager (CPM) -Pharma- Basel, Switzerland, CHF 600-950.
My client is a major Pharmaceutical company looking for an on-site CPM to start ASAP. Deadline is on the 3rd of June.
ROLE RESPONSIBILITIES
Responsible for operational aspects of assigned clinical studies (interventional and non-interventional) under the lead of Senior Clinical Project Manager (Sr. CPM).
Together with the Sr. CPM , the Clinical Operations Specialist (COS) and the Team, the successful candidate will ensure adequate trial execution from protocol generation to clinical trial report/manuscript writing. He/she will be responsible for ongoing and effective collaboration with Sponsor, Line Functions (medical writing, statistics, data management, monitoring, etc.) and third-party vendors. Specific activities include:
1. Ensure trial deliverables are met according to timelines, budget, quality standards and operational procedures.
2. Work with the Sr. CPM on investigators' meeting organization and all internal meetings related to the clinical trial execution and operational excellence.
3. Contribute to the trial data ongoing medical/scientific quality review.
4. Project/trial allocation plans within given indications and implementation to ensure optimum patient accessibility, resource utilization/allocation and country.
5. Ensure and sign off high quality Monitoring Plans and other study plans and reports.
6. Identify potential operational issues and implement actions to resolve them.
SKILLS and BACKGROUND DESIRED
Education (minimum/desirable): Advanced degree or equivalent education/degree in life science/healthcare is required.
Languages: Fluent English (oral and written).
Experience/Professional requirement:
1. 8 years' Clinical Operations experience with at least 4 years managerial experience in planning, executing, reporting and publishing clinical studies (interventional and non-interventional) in a pharmaceutical company or contract research organization.
2. Proven ability to work independently in a complex matrix environment (including remote).
3. Good project management skills.
4. Thorough knowledge of Good Clinical Practice, clinical trial design, statistics, regulatory processes, and global clinical development process.
5. Demonstrated presentation and diplomacy skills. Negotiation and conflict resolution skills.
6. Strong customer oriented mindset
7. Ability to resolve issues with minimal supervision and understand when to escalate.
8. Willingness to act accountably in project/trial management.
HOW TO APPLY?
Please contact Arnaud Heroult on +44 (0)203 096 4712 or email arnaud.heroult@srgclinical.com if you would like to know more about this opportunity.
The recruiter has stated that all applicants for this job should be able to prove they are legally entitled to work in the EU. SRG is a trading name of Science Recruitment Group Ltd an Employment Business/Agency.
