Description
Global Medical Information Manager (m/f)
Reference: -en
Start: asap
Duration: 12 MM++
Main tasks:
- Develop responses for simple and complex medical inquiries: Formulation of the strategy and framework within which a response lies
- Conduct comprehensive literature searches in relation with a medical inquiry: Identify and weigh the information available
- Prepare, finalize, and update global standard response documents, based on knowledge of clinical studies, therapeutic areas, and new information appearing in the literature
- Communicate with internal reviewers to finalize documents
- Compile and maintain comprehensive, accurate, and up-to-date Competitor Compendiums to provide Clinical Development with scientific and clinical insights on products and treatment trends for new disease areas
- Develop and maintain good relationships with internal departments and external contacts
- Provide an information support service to the clinical and marketing teams including the distribution among other departments of data relating to medical information inquiries and Global Response Documents (GRDs) as well as ad hoc, bespoke activities relating to medical information that support the broader needs of the organization
- Propose process improvements to enhance the global medical information service from a methodology, process, and compliance perspective
- Manage and track inquiries with standard medical information databases
- Transmit any reported adverse events to Global Drug Safety (GDS) in a timely manner
Main qualifications
- PhD or PharmD level degree, with thorough grounding in clinical pharmacotherapy
- Must have a broad knowledge and understanding of products and diseases that allows for the provision of complex information that is accurate and meets all regulatory requirements
- Can understand and apply principles, concepts and standards
- Previous pharmaceutical industry experience in medical information, medical communication, or regulatory affairs
- Knowledge of relevant information sources including: Printed publications, unpublished sources, databases, websites, company departments, external bodies
- Ability to analyze and appraise clinical, biomedical, and scientific reports in a systematic, fair, and balanced way
- Ability to work with ambiguity and complex situations
- Excellent organizer and communicator
- Ability to work independently and as part of a team
- Experience in international settings
- Fluent in written and spoken English
- Demonstrated scientific/medical writing experience
- Good knowledge of Microsoft (MS) Office tools, especially MS Word
Main advantages:
- Interesting tasks in a multinational environment
- A city with a high quality of life that perfectly embraces both modern and traditional values
About us:
With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.
My contact at Hays:
My contact person:
Svenja Weiß
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