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Health Care 🏢 Full Time ⭐️ Verified

Senior Clinical Research Associate (CRA)

MediCore Innovations
London
Salary Estimate
GBP 55.000 – GBP 70.000
Live Update
15 Mei 2026
Deadline
15 Mei 2027

Job Description

Are you a results-oriented professional passionate about accelerating medical breakthroughs? MediCore Innovations is seeking a highly skilled Senior Clinical Research Associate to join our dynamic team in London. In this pivotal role, you will oversee clinical trials, ensuring compliance with Good Clinical Practice (GCP) while driving the development of life-changing therapies.

We offer a competitive benefits package, including flexible working hours, private medical insurance, and a clear pathway for career progression within a global leader in healthcare.

Why Join Us?

  • Work on cutting-edge therapeutic areas.
  • Access to continuous professional development and certifications.
  • A supportive, inclusive culture that values diversity.

Responsibilities

  • Monitor clinical trial sites to ensure compliance with GCP, protocol, and regulatory standards.
  • Manage relationships with Principal Investigators, study coordinators, and study sites to ensure data integrity.
  • Review and interpret data from Case Report Forms (CRFs) and source documents to identify and resolve discrepancies.
  • Conduct regular site visits and perform interim and close-out monitoring.
  • Prepare comprehensive monitoring reports and submit them to the Clinical Operations team.
  • Facilitate effective communication between sponsors, investigators, and regulatory bodies.
  • Ensure timely initiation, conduct, and completion of clinical studies according to the project timeline.

Qualifications

  • Minimum of 3-5 years of experience as a Clinical Research Associate, preferably in the UK or Europe.
  • Relevant Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or Medicine (Masters preferred).
  • Valid GCP certification (e.g., ACRP or EFPIA) is mandatory.
  • Strong understanding of regulatory affairs and clinical trial processes.
  • Excellent written and verbal communication skills.
  • Willingness to travel up to 60% of the time to various study sites.
  • Proficiency in using electronic data capture (EDC) systems such as Medidata Rave or Oracle Clinical.

Required Skills

Clinical Trials GCP Data Management Regulatory Affairs Site Monitoring Medical Writing Interpersonal Communication

Ready to Take on This Challenge?

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