Clinical Project Manager

An exciting opportunity has arisen for an experienced Clinical Project Manager to join a privately-owned full service global CRO. This role will be based in Cheshire on a permanent basis. The successful candidate will project manage sponsor clinical trials to applicable regulatory guidelines and Good Clinical Practice (ICH GCP) standards, within agreed timelines and stated budgets. This position will report to the Head of Clinical Operations based in our UK Headquarters in Knutsford, Cheshire.

The role will require you to be educated to degree level or equivalent in a scientific field with proven clinical project management experience within a CRO or pharmaceutical company; a full driving licence together with a willingness to travel.

Key Responsibilities:

• Ensure that all company clinical studies conducted are in accordance with Good Clinical Practice guidelines (GCP) and are completed on time and within the stated budget
• Generate clinical project plans and oversee adherence to ensure business objectives and key deliverables are met
• Contribute to the clinical trial design and the identification of potential study sites where necessary
• Oversee and manage the development and approval of clinical trial documentation
• Oversee and manage timely clinical trial submissions to ethics authority and assist where possible in regulatory applications in order to proceed with clinical studies
• Management of any specialist vendors contracted by the company in relation to day to day operations of assigned clinical trials and to ensure that study timelines and deliverables are being achieved as contracted
• Develop ongoing relationships and define project milestones as the primary contact with the sponsor
• Ongoing risk assessment and management
• Ongoing evaluation of project strengths, weaknesses and potential areas for improvement
• Build effective relationships internally at the company and externally with the Sponsor/Contractors

Key skills required:

• Pharma/CRO experience would be an advantage
• Excellent project management and personnel management skills Clinical Project Manager (CPM)
• Fluent written and oral English language including familiarity with medical terminology
• Professional interpersonal and communication skills
• Ability to work with minimum supervision and to prioritise tasks
• A flexible and adaptable attitude
• Ability to problem solve
• Numeracy and good attention to detail
• Excellent time management skills
• Self-motivation and enthusiasm

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Theodora Savlovschi-Wicks on +44 203 7520 314 or upload your CV on our website - www.Proclinical.com.
A full job description is available on request.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.