Medical Information (MI) Pharmacist
| Dyddiad hysbysebu: | 02 Hydref 2025 |
|---|---|
| Cyflog: | £38,000 bob blwyddyn |
| Oriau: | Llawn Amser |
| Dyddiad cau: | 01 Tachwedd 2025 |
| Lleoliad: | SM3 9BW |
| Gweithio o bell: | Ar y safle yn unig |
| Cwmni: | TriOn Pharma Limited |
| Math o swydd: | Parhaol |
| Cyfeirnod swydd: | TRI/MI |
Crynodeb
The MI Pharmacist will be responsible for providing accurate, balanced, and timely medical and product information to healthcare professionals, patients, and regulatory authorities. The role will ensure compliance with the ABPI Code of Practice, MHRA requirements, and company policies.
Key responsibilities will include:
Responding to medical information enquiries from healthcare professionals, patients, and distributors.
Reviewing and approving promotional and non-promotional materials in accordance with the ABPI Code of Practice.
Monitoring and reporting adverse events in compliance with pharmacovigilance requirements.
Maintaining an up-to-date knowledge base of TriOn Pharma’s products and therapeutic areas.
Liaising with Regulatory Affairs, Pharmacovigilance, and Commercial teams to ensure consistent and compliant messaging.
Providing medical and scientific training to internal teams as required.
Assisting in the preparation of product monographs, summaries, and technical documents.
Skills, Experience, and Qualifications Required:
Master’s degree in Pharmacy (MPharm) and registration with the General Pharmaceutical Council (GPhC).
Minimum 2 years’ experience in a medical information, regulatory, or clinical role within the pharmaceutical industry.
Detailed understanding of the ABPI Code of Practice and MHRA regulations.
Strong communication skills and the ability to provide clear, evidence-based responses.
Knowledge of pharmacovigilance processes and adverse event reporting.
Key responsibilities will include:
Responding to medical information enquiries from healthcare professionals, patients, and distributors.
Reviewing and approving promotional and non-promotional materials in accordance with the ABPI Code of Practice.
Monitoring and reporting adverse events in compliance with pharmacovigilance requirements.
Maintaining an up-to-date knowledge base of TriOn Pharma’s products and therapeutic areas.
Liaising with Regulatory Affairs, Pharmacovigilance, and Commercial teams to ensure consistent and compliant messaging.
Providing medical and scientific training to internal teams as required.
Assisting in the preparation of product monographs, summaries, and technical documents.
Skills, Experience, and Qualifications Required:
Master’s degree in Pharmacy (MPharm) and registration with the General Pharmaceutical Council (GPhC).
Minimum 2 years’ experience in a medical information, regulatory, or clinical role within the pharmaceutical industry.
Detailed understanding of the ABPI Code of Practice and MHRA regulations.
Strong communication skills and the ability to provide clear, evidence-based responses.
Knowledge of pharmacovigilance processes and adverse event reporting.