Clinical Project Manager

Hobson Prior are currently looking for a Clinical Project Manager to join a leading CRO who has over 40 years of global experience, with a global team dedicated to bringing ophthalmic innovations to the market. This is a permanent position based in the US.

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

Job Responsibilities:

• To manage cross functional project teams derived from the groups within clinical development to deliver a high-quality clinical trial(s) in compliance with all regulations and SOPs.
• Reviews protocol, source documents and CRFs and tracks them to completion.
• Works with functional areas on initiating, planning, executing, controlling, closing and resourcing clinical trial projects.
• Accountable for creating and maintaining project timelines for each project and uses these timelines to track and manage a project's progress.
• Accountable for creating Project Plans (Roles and Responsibility Tables and Communication Plans) and weekly project budget and progress reviews for each study.
• Reviews study metrics for performance and quality with the team and management.
• Prepares high-quality reports (financial, project, etc.) for management on program status and issues.
• Ensures review of clinical electronic Trial Master File (eTMF) for completeness.
• Manages and coordinates all vendors involved in the clinical trials (e.g. central labs, IVRS, reading centers).
• Responsibilities may differ slightly from the above based on specific needs of the business.
• Clear and sustained demonstration of the organisation's Clinical's Values of Customer Service, Leadership, Accountability, Results Oriented, Innovation and Teamwork.
• Any other assigned duties.

Key Skills:

• Ability to establish and maintain effective professional relationships with co-workers, managers and clients.
• Highly effective organizational and communication skills.
• Ability to plan, identify risks, anticipate issues and outcomes, and respond strategically, tactically and operationally while balancing short-term and long-term company objectives.

Requirements:

• Bachelor's degree in Life Science with at least 5 years of clinical trial experience. Years of experience may be considered in lieu or education.
• At least 1 year of clinical project management experience.
• Ophthalmology experience is admirable.
• Understanding of multi-center drug and/or device trials.
• Experience with Veeva TMF and CTMS systems.
• Demonstrated expertise of applicable regulatory requirements and GCP.
• Demonstrated leadership skills and the ability to multitask and to solve problems proactively.
• Proficiency with Excel, PowerPoint and vendor management.
• Travel of up to 15% is required (mainly domestic, overnight).

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.