Clinical Project Manager

Clinical Project Manager

Based in Europe

Small/Mid-Sized CRO.

£70,000 - £80,000

This little gem of a CRO are such a delight to represent. Everything they stand for and everything they are implementing, both within the company and the trials they are supporting, are testament to them being an amazing company to work for.

Although they are only a team of c700 globally, they are packing a punch in the clinical world and due to expansion, are looking for a Clinical Project Manager to come in and continue the excellent work they already carry out.

You will be Responsible for management and oversight of assigned clinical research trials (Phase I through Phase IV) to ensure client’s goals of time, cost, and quality performance are met.

Some of the duties you will be required to undertake are below:

• Plan, implement, evaluate, and complete full execution of assigned clinical trials
• Set goals and timelines, provide oversight and foster motivation within the team to accomplish goals within defined timelines and with high quality in the execution of assigned clinical trials
• Provide oversight and coordination of the operational aspects of the functional areas on assigned projects to ensure compliance with International Council for Harmonization (ICH) guidelines, Good Clinical Practices (GCP), applicable regulatory guidelines and trial procedures
• Provide management of full scope clinical trial projects including global trials from start-up through analysis phase; provide oversight of functionally assigned teams members on clinical trials projects; manage multiple projects simultaneously
• Provide coordination of a clinical trial project including organization, implementation, and management of scoped activities
• Prepare or provide oversight to the development of trial plans and timelines; work with the trial-assigned Director or line manager to provide effective solutions to challenges that arise during the clinical trial project
• Participate in or provide oversight and guidance in the development of trial required deliverables Serve as client contact at project operational level
• Provide oversight to contracted vendors; review contracted specifications and maintains regular interactions with vendors to ensure meeting timelines and expectations
• Demonstrated strong knowledge and clear understanding of SOPs

Required Candidate Background

• Bachelor’s degree or equivalent, preferably in allied health fields such as nursing, pharmacy, or health science, preferably with clinical trial management experience
• 4 to 6 years clinical research experience (CRO CRA or Clinical Research Manager, Site Coordinator or Research Manager, Clinical Research Laboratory Manager) or possesses transferrable skills and experience in project management in a clinical setting or relatable industry

If you are considering a change within your career and want to work for a CRO who do things differently, and one who will support your growth and put time into nurturing your skills, please contact Paul Adam on 01293 364079 or send me a copy of your CV to paul.adam@rbwconsulting.com

This is one of the many opportunities I am working on across Europe. If your profile isn’t quite right but you know someone who is looking for a change, I would be interested in having a confidential discussion about how I may be able to assist.

I look forward to hearing from you