Senior Patient Safety Specialist Job – Cambridge, UK
- Ref: 20826
An exciting opportunity is now available for a Senior Patient Safety Specialist to join an established biopharmaceutical company in Cambridgeshire. The position will require you to triage safety reports for regulatory reporting purposes. You will lead the preparation of aggregate reports including PSUR, periodic reports and EU Annual Safety Reports. Previous experience at a similar level is required.
Clinical Safety Scientist Job – Surrey, UK
- Ref: 20821
We are recruiting for Clinical Safety Scientist to join a Pharmaceutical company in Surrey on a contract basis. The daily responsibilities will include the continued safety monitoring and evaluation of assigned company products (primarily in the post-marketing setting), ensuring compliance with regulatory requirements. You will author periodic regulatory documents, requiring proven experience in this area.
Medical Information Associate Job – Middlesex, UK
- Ref: 20781
One of the top and most widely respected global Pharmaceutical companies is offering a Medical information associate position in their company based in Middlesex. Their aim is to successfully develop innovative medicines and products that help millions of people around the world. The successful candidate will provide up-to-date and relevant medical, technical and pharmaceutical information on the company’s marketed, discontinued or pipeline products to internal and external customers. You will liaise with doctors, pharmacists, nurses, patients and company representatives. Previous experience working in a similar position is essential.
Pharmacovigilance Surveillance Scientist Job – UK/Germany
- Ref: 20763
An exciting opportunity is available for a Drug Safety Surveillance Scientist to join a Pharmaceutical company in Cambridgeshire in a permanent part-time position. Experience in safety surveillance of pre-and post-marketed products in accordance with European and ICH guidelines is essential. Particular expertise on PSUR preparation and timelines, signal detection, and risk management is required. The days you could work would be flexible.
Assistant PA Job – Hertfordshire, UK
- Ref: 20725
A new position as Assistant PA is now available with a CRO based in Hertfordshire. You will provide administrative and secretarial support to the PA to the Board. Previous administration or secretarial work experience would be preferred.
Drug Safety Manager Job – Surrey, UK
- Ref: 20623
We are recruiting for a Manager of Drug Safety Services to join an established company in West Sussex or Berkshire. The position will require you to line manage a team of associates and lead global projects. Part of your responsibilities will require you to contribute to the Quality aspects of the team’s output. Experience in safety surveillance, case management and knowledge of Periodic Safety Update Report writing is desirable. Knowledge of Good Clinical Practice (GCP) related to clinical safety documentation worldwide regulatory requirements would beneficial.
Manager of Drug Safety Services Job – West Sussex, UK
- Ref: 20582
We are recruiting for a Manager Of Drug Safety Services to join an established company in West Sussex. The position will require you to line manage a team of associates and lead global projects. Part of your position will require you to contribute to the Quality aspects of the team’s output. Experience in safety surveillance, case management and knowledge of Periodic Safety Update Reports are desirable. This position offers the opportunity to work across two offices, based in Crawley and Maidenhead.
Drug Safety (Contract) Job – Cambridge, UK
- Ref: 20417
We are recruiting for Drug Safety Officer to join a Pharmaceutical company in Cambridgeshire on an 11-month contract. You will be working within the Medical Department and reporting to the Drug Safety Manager, responsible for ensuring adherence to company’s UK & Ireland’s regulatory commitment for pharmacovigilance. You will need to have relevant industry experience within pharmacovigilance or clinical research. Strong communication skills at business level English language ability are required for this role. Previous experience is essential.
Medical Info and Drug Safety Associate Job – Chichester, UK
- Ref: 20803
We are recruiting for one of the largest and widely respected global medical devices companies that are offering a Medical Information and Drug Safety Associate position. The successful candidate will perform literature searches for pharmacovigilance, medical information and business development purposes. You will follow-up on spontaneous reports with consumers and healthcare professionals. Previous experience in Drug Safety or Medical Information is desired.
Want to find out more?
Contact CK Clinical’s specialist Drug Safety and Pharmacovigilance Recruitment Consultant on 01438 743 047 or email email@example.com