Clinical Project Manager

Hobson Prior are seeking a Clinical Project Manager to join a brilliant pharmaceutical company on a permanent basis, located in Welwyn Garden City. Our Client is focused on improve the lives of patients with medicines and diagnostics.

Please note that to be considered for this role you must have the right to work in this location.

Key Responsibilities:

• In this position you will be responsible for assuring compliance with ICH-GCP guidelines, SOPs, and all regulatory requirements through global and regional study management teams.
• Establish and monitor project scope, timelines, and deliverables.
• Reconcile project plan with contract requirements.
• Monitoring and status reporting on study targets, including communication, risk and quality planning and oversight of team members.
• Regularly schedule and document project team meetings.
• Track implementation of resolutions to completion by assessing project issues, recommending resolutions to management and Steering Committee members as necessary.
• Manage supplies and resources in adherence with project timelines, budgets, and quality standards to ensure the quality of project services and deliverables.
• Keep study team and management informed of study status and escalate unresolved issues.
• Ensure the TMF is maintained in a proper manner.
• Tracking site payments, financial agreements, and contracts.
• Attending and contributing to Investigator meetings.
• Managing the ethical, legal, and regulatory environment locally and globally, as well as managing applications.
• Assuring delivery of contracted scope of work for assigned regions and countries.
• Make a contribution to the improvement of the process.
• Ensure timely and accurate communication to key stakeholders.
• Managing clinical trial budgets, including CRO and vendor contracts.
• Initiating and maintaining harmonious relationships with vendors and partners.

Requirements:

• Strong communication and organizational skills (required).
• Strong understanding of ICH/GCP and other regulatory requirements (essential).
• Experience managing clinical trials within a pharmaceutical, biotechnology, medical device or CRO (required).
• Ability to take a flexible approach on a day-to-day basis (essential).
• Ability to work effectively in multidisciplinary teams (essential).
• Demonstrated ability to exhibit high levels of professionalism both internally and externally (essential).
• Experience with early/late-stage clinical trials (preferable).

Apply now:

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.