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United Kingdom ADVANZ PHARMA Full timeJob Title: Medical Science Liaison - (Biosimilars) Location: UK MUST HAVE EXPERIENCE IN BIOSIMILARS About the Role The Medical Science Liaison works as part of the Medical Office team and is embedded in the Medical Affairs department of the UK & Ireland affiliate, specifically to: Deploy the Medical Affairs strategy, as discussed with management at...
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Medical Science Liaison
1 week ago
United Kingdom ADVANZ PHARMA Full timeJob Title: Medical Science Liaison - (Biosimilars) Location: UK MUST HAVE EXPERIENCE IN BIOSIMILARS About the RoleThe Medical Science Liaison works as part of the Medical Office team and is embedded in the Medical Affairs department of the UK & Ireland affiliate, specifically to:Deploy the Medical Affairs strategy, as discussed with management at a national...
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Medical Science Liaison
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United Kingdom ADVANZ PHARMA Full timeJob Title: Medical Science Liaison - (Biosimilars) Location: UK MUST HAVE EXPERIENCE IN BIOSIMILARS About the Role Deploy the Medical Affairs strategy, as discussed with management at a national level and approved by the Global Director Medical Affairs, through development and execution of a local MSL plan Contribute towards medical strategy for...
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Medical Director
1 week ago
Our client, a leading Contract Research Organisation (CRO), is seeking an experienced Medical Director to provide strategic medical leadership for clinical trials across diverse therapeutic areas. This is an exceptional opportunity to work with a dynamic team, driving innovation in global clinical research. Candidates can work remotely in any of the following locations: UK, Italy, Poland, Spain, Hungary, Romania, Germany, France, Serbia or Slovakia.
Key Responsibilities
- Oversee the medical and scientific integrity of clinical trials from protocol development to completion.
- Act as the primary medical liaison with sponsors, regulatory agencies, and internal teams.
- Provide safety oversight and ensure adherence to ICH-GCP guidelines and regulatory requirements.
- Contribute to regulatory submissions, clinical study reports, and safety reviews.
- Support business development efforts by providing medical expertise during client discussions.
Qualifications
- MD/DO with a valid medical license.
- 5+ years of clinical research experience, preferably within a CRO or pharmaceutical environment.
- Strong knowledge of clinical trial processes, GCP, and regulatory frameworks.
- Excellent communication and stakeholder management skills.