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Health Care 🏢 Full Time ⭐️ Verified

Senior Specialized Medicine Specialist - London

ApexMed Specialty Medicine
London, England
Salary Estimate
GBP 65.000 – GBP 120.000
Posting Time
6 Mei 2026
Deadline
6 Mei 2027

Job description

Join ApexMed, a premier leader in specialized medicine, where clinical excellence meets patient-centered care. We seek a skilled Specialist in Specialized Medicine to drive research, clinical operations, and cross-functional collaboration in London.

In this role, you will lead and influence advanced clinical programs, contribute to pharmacovigilance and regulatory submissions, and shape medical strategy across therapeutic areas including rare diseases and oncology.

We offer a collaborative, high-performance environment with access to state-of-the-art facilities, ongoing professional development, and competitive compensation.

Responsibility

  • Lead design, coordination, and execution of complex, registry-based and clinical trials in rare diseases and oncology.
  • Collaborate with physicians, scientists, regulatory affairs, and commercial teams to ensure study integrity and timely delivery.
  • Oversee pharmacovigilance activities, safety reporting, and risk management plans.
  • Mentor junior clinicians and clinical research staff; drive high-quality data capture and governance.
  • Prepare regulatory submissions and contribute to medical affairs and publication strategies.
  • Develop and implement evidence-based care pathways and quality improvement initiatives.
  • Present findings at national/international conferences and author manuscripts for peer-reviewed journals.

Qualification

  • Medical degree (MBBS/MD) with board certification in a relevant specialty or equivalent.
  • Minimum 5 years of experience in specialized medicine, clinical research, or pharmacovigilance.
  • Proven track record leading cross-functional teams across clinical, regulatory, and commercial functions.
  • Strong knowledge of GCP/ICH guidelines, regulatory requirements, and study design.
  • Demonstrated publication history and experience in clinical trial management.
  • Excellent communication, negotiation, and stakeholder management skills.
  • Proficiency with data analysis tools (e.g., SAS, R, Python) is a plus.
  • Right to work in the UK or valid visa; willingness to relocate to London if applicable.

Required Skills

clinical research pharmacovigilance medical writing data analysis regulatory affairs cross-functional collaboration patient care trial management

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