Medical Affairs / Drug Safety Pharmacists >
Description.
Support medical affairs and pharmacovigilance functions within pharmaceutical companies, regulatory environments, and drug-safety teams. Contribute to medical information activities, safety monitoring, evidence review, and compliant communication of medicines information across healthcare and industry settings.
Key Requirements.
Experience.
Minimum 1 year’s post-registration experience in medical affairs, drug safety, or pharmacovigilance.
Skilled in reviewing clinical evidence, responding to medical information enquiries, and supporting compliant promotional and non-promotional activities.
Experience in drug-safety case processing, signal detection, literature surveillance, or regulatory reporting.
Confident working with cross-functional teams including regulatory, medical, safety, commercial, and quality.
Qualifications.
MPharm degree (or recognised equivalent) with full GPhC registration.
Postgraduate training in Medical Affairs, Pharmacovigilance, Drug Safety, or Clinical Pharmacy desirable.
CPD in regulatory standards, safety reporting requirements, and evidence-based medicine.
Compliance and Vetting.
Enhanced DBS on the Update Service.
Full identity and right-to-work verification.
Two recent professional references.
Up-to-date mandatory training relevant to industry or office-based roles.
Immunisation compliance where roles involve clinical or hospital-based activity.
Full GPhC registration and fitness-to-practise check.
Verification of qualifications and employment history.