- Lead medical oversight for clinical studies, including protocol development and Quality‑by‑Design principles.
- Act as medical monitor: safety review, medical queries, oversight of study conduct.
- Support development of CRFs, Medical Monitoring Plans, and Clinical Study Reports.
- Maintain strong relationships with investigators and clinical sites.
- Provide medical input to pharmacovigilance activities for clinical and post‑authorisation studies.
- Review clinical and safety data; identify risks and propose solutions.
- Ensure inspection readiness and support GCP audits/inspections.
- Contribute to process improvements, digital trial initiatives, and cross‑functional knowledge transfer.
- Provide internal scientific training and represent the organisation at scientific meetings.
- Support communication with regulatory authorities as required.
- MD (or equivalent) from UK, EU, or USA.
- 3+ years' experience in clinical research/clinical development.
- Strong knowledge of ICH/GCP and global clinical trial regulations.
- Experience in medical monitoring, protocol development, and clinical data review.
- Excellent written and verbal communication skills.
- Strong analytical, decision‑making, and project leadership abilities.
- Ability to work independently, manage deadlines, and solve problems quickly.
- Competitive salary and benefits.
- Opportunity to impact patient care and contribute to meaningful scientific progress.
- High exposure to senior scientific experts and strategic programs.
- Collaborative, intellectually driven environment focused on clinical excellence.
- Hybrid work model with two days on‑site.
- Medical Doctor
- Clinical Development
- Clinical Trial Management
- Medical Monitoring
- Protocol Development
- Quality by Design (QbD)
- Pharmacovigilance
- ICH/GCP Compliance
- Clinical Data Review
- Medical Affairs
- Cross‑functional Leadership
- Investigator Engagement
- Clinical Site Management
- Risk Management
- Clinical Project Management
- SOP Development
- Scientific Communication
- Regulatory Interaction
- Inspection Readiness
- Audit Support
- Clinical Strategy
- Medical Governance
- Stakeholder Management
- Scientific Writing
- Problem Solving
- Time Management
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Medical Manager - Greater London - EPM Scientific
Description
Overview
I am currently hiring for an international specialty pharmaceutical organisation advancing innovative treatments. I am looking for a Medical Manager to provide scientific and medical leadership across clinical programs, ensuring high‑quality study design, execution and oversight.
Key Responsibilities
Requirements
What You Get
Desired Skills and Experience
If this aligns with your expertise and ambition, I invite you to take the next step and apply.
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Medical Manager
Only for registered members London
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Medical Governance Manager
Full time Only for registered members England
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Medical Project Manager
Full time Only for registered members United Kingdom
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Medical Case Manager
Only for registered members London
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Medical Case Manager
Only for registered members London, UK
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Medical Affairs Manager
Only for registered members London
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Manager, Medical Affairs
Only for registered members London, United Kingdom
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Medical Communications Manager
Only for registered members London
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Manager, Medical Affairs
Only for registered members London, England
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Medical Affairs Manager
Only for registered members London
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Medical Affairs Manager
Only for registered members London, England
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Medical Affairs Manager
Only for registered members Greater London, England
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Medical Affairs Manager
Only for registered members London Area
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Medical Governance Manager
Only for registered members England
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Medical Communications Manager
Only for registered members London, England
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Manager, Medical Affairs
Only for registered members London
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Medical Clinic Manager
Only for registered members London WU HW
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Senior Manager Medical Writing
Only for registered members London
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Expert Medical Information Manager
Only for registered members London
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Expert Medical Information Manager
Full time Only for registered members London
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Senior Manager Medical Writing
Full time Only for registered members London