Hobson Prior are looking for a Clinical Trial Manager to join a biopharmaceutical research organisation who specialize in oncology product development and pioneering medicines that are used all over the world. This is a permanent position located in Switzerland.

Job Responsibilities:

• You will be accountable to deliver Trials on time, within budget, and with highest achievable quality.
• Responsible for feasibility and lead the evaluation and selection of countries and investigative sites.
• You will assist in the review, development and/or writing of clinical trial documents and manuals.
• Develop and manage trials timelines and budget.
• Select, coordinate and monitor activities of vendors.
• Coordinate data cleaning and review.
• You will ensure set up and maintenance of all systems in order to plan and implement trials and track progress.
• Generate reports to update management on conduct of trials.
• Ensure appropriate clinical trial supply plans are implemented and managed.
• Develop recruitment plans, risk-mitigation plan, monitor and implement contingencies as required.
• Partake in monitoring study safety.
• Review key study quality metrics (e.g., eligibility, primary endpoint data, etc.) and determine appropriate action in conjunction with study team.
• Complete initial review of CRO and other third-party study vendor invoices to ensure that work is performed in accordance with scope of work.

Key Skills:

• Ability to effectively manage multiple priorities across several protocols and therapeutic areas simultaneously.
• Demonstrated leadership and problem-solving skills.
• Good planning, prioritization, problem solving and organizational skills; strong customer-orientation, used to work independently.
• Excellent communication skills used to communicate with a broad range of stakeholders and to build strong positive relationships.

Requirements:

• BS/BA degree or a relevant degree with strong emphasis on science.
• A minimum of 3 years' experience in the biopharmaceutical industry or other relevant clinical research experience in the conduct and management of multinational clinical trials.
• Must have working knowledge of ICH Good Clinical Practices and other relevant regulatory/health authority experience.
• Experience in executing a wide range of clinical trial activities (from initiation to clinical study report).

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.