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We are seeking a Senior Manager, Global Evidence Generation and Medical Operational Excellence (SMEG‑OE) to join our Medical Affairs organisation in London. Reporting to the Chief Medical Officer, this global role will play a pivotal part in overseeing evidence generation activities and driving medical operational excellence across Theramex. You will lead and manage the Global Scientific Review Committee (G‑SRC) and provide operational leadership across global medical planning, repositories, and medical meeting management. This position requires deep expertise in GCP, GPP, clinical research, publication standards, and strong organisational and communication skills to ensure compliance, operational rigour, and effective dissemination of scientific activities.
Job Responsibility:
Serve as the Chairperson of the G‑SRC, ensuring effective leadership and smooth committee operations
Review and evaluate: Theramex‑sponsored non‑interventional studies from affiliates and therapeutic area heads
Post‑Authorisation Safety Studies (PASS)
Investigator‑Initiated Studies
Ensure submissions align with scientific merit, regulatory standards, and Theramex research priorities
Organise and lead regular G‑SRC meetings and other medical meetings
Develop and distribute meeting agendas
Prepare accurate and timely meeting minutes capturing decisions, actions, and follow‑ups
Track and manage action items, ensuring appropriate follow‑up with stakeholders
Ensure study proposals, minutes, correspondence, and approvals are documented and stored in compliance with company and regulatory requirements
Maintain a comprehensive, organised system for evidence generation documentation
Oversee compliance with GCP, GPP, and all relevant regulatory guidelines
Lead preparation and review of publications (manuscripts, abstracts, posters)
Ensure all publications adhere to GPP and internal policies
Collaborate cross‑functionally to support the publication strategy and timely dissemination of results
Partner with global medical teams, regulatory affairs, pharmacovigilance, and other stakeholders to maintain aligned evidence generation priorities
Act as the main point of contact for affiliates and therapeutic area heads on evidence generation processes
Facilitate efficient communication and decision‑making across stakeholder groups
Lead global medical budget planning and monitoring
Maintain and regularly update global medical repositories
Organise global medical meetings and ensure operational consistency across teams
Requirements:
An advanced degree (MD, PhD, PharmD, or equivalent)
Experience in clinical research, medical affairs, or clinical trial management (including non‑interventional studies and investigator‑initiated studies) within the pharmaceutical or biotech industry
Expertise in Good Clinical Practice (GCP) and Good Publication Practice (GPP)
Global experience and comfort operating across multiple therapeutic areas (highly desirable)
Excellent project management capabilities with the ability to manage multiple priorities and stakeholders
Strong communication and presentation skills, with the ability to communicate complex scientific topics clearly
Outstanding organisational skills with strong attention to detail and documentation accuracy
Strong leadership, collaboration skills, and the ability to influence stakeholders at all levels
A proactive and solution‑oriented mindset, with passion for scientific research and evidence generation
Ability to work independently and as part of a global, cross‑functional team in a fast‑paced environment
Willingness to travel occasionally for meetings, conferences, or study‑related activities
What we offer:
A fast‑paced environment with broad exposure, where you can grow—even beyond your current expertise
A culture that supports learning, celebrates success, and recognises performance
Opportunities for ambitious, talented professionals who want to be part of our purpose‑driven journey