Pharmacovigilance Manager

Hobson Prior are recruiting for as a Pharmacovigilance Manager to join a research-based biopharmaceutical company in Cambridge. Our client is very patient-focused, whose scientific research has benefitted hundreds of thousands of people by ensuring medications are available to those who could otherwise not afford them.

Job Responsibilities:

• Author and coordinate cross functional contributions to Clinical Trial Safety Reporting Procedures.
• Co-operate with internal and external parties to clarify any inconsistencies or issues with responsibilities and terms and conditions described in the CTSRP.
• Highlights areas of concern to manager; able to make recommendations for and implement processes for improvement.
• Competent in abilities in area of expertise and the wider areas of PVE.
• Able to gather information or assign tasks or activities for a given project with minimal direction.
• Acts as project lead.
• Establishes work priorities with minimal direction from manager. Work is performed without appreciable supervisory direction.
• Delivers regular updates to manager, including challenges and suggested actions that could be taken.
• Able to maintain confidentiality (especially on patient records), with good attention to detail and a high level of concern for accuracy and quality.
• Actively participates in S&C meetings and shares information on projects and challenges openly.
• Recognizes potential or impending problems, implements and delivers solutions.
• Maintains compliance with PVE and applicable SOPs and work instructions.
• Maintains knowledge of company disease and therapeutic areas.

Key Skills:

• Demonstrates excellent scientific/clinical or analytical knowledge base, with ability to assess data and understand the safety/medical or process implications.
• Demonstrates excellent verbal and written communication skills.
• Excellent attention to detail, teamwork and initiative.
• Able to plan effectively to create, update and maintain CTSRPs in a timely manner.
• Has an appropriate level of IT skills in Microsoft Excel, PowerPoint and Word.

Requirements:

• Scientific background with a medico-scientific university degree.
• Prior experience in multiple aspects of pharmacovigilance activities.
• Project management experience preferred or experience in managing complex projects.
• Working knowledge of global safety regulatory requirements.

Apply now:

If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back 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.