- Regulatory Affairs CMC Manager / South-East / Join a Biologics company with a Great Pipeline
We have a new role based in the South-East for a Top Ten Biotechnology company who require a CMC Regulatory Affairs Manager to cover development, registration and approval/post approval activities. This is varied and highly strategic CMC at a Global Head office. Contact Theo Moore on +44(0)207 801 3384 to apply for this role or send your CV in confidence to CV@advregulatory.com.
- Clinical Exploratory Project Manager – Contract role - Global Company based in the South-East – Great rate and good project
This role is on exclusive assignment to Advanced Search & Selection. Please contact Theo Moore or Matt Greig initially on +44 20 7801 3380 or +44 7918 679 405 (until 9.00 pm CET and Saturday mornings) or send a full CV and contact information to email@example.com or firstname.lastname@example.org who will support your assessment and on-boarding process.
- Regulatory Affairs Project Manager - CMC
Regulatory Affairs Project Manager - CMC £42,000-£47,000 per annum. Are you looking to work for a pharmaceutical consultancy in the heart of London?
Is working on CMC/biologics from pre-clinical through to post-approval of interest to you?
- Pharmacovigilance - Senior Project Manager
I am currently seeking Senior PV Project Manager or PV manager to joing an exciting and ambitious company based in Surrey on a permanent basis. The role has been created as a result of expansion and will suit someone who thrives in fast paced environments
- PW 6585 CPM / Clinical Project Manager
Opportunity to join this energetic, ambitious and growing Global CRO at CPM level. You’ll be a strong team member and understand the need for effective communication at all levels. You will have a demonstrable record for effective relationship building with clients and colleagues. You’ll be confident in presenting at Ethic committees and sponsors and have high standards for the quality of material presented. UK and EU trials across therapy, some focus on Oncology.
- Drug Safety Project Manager
My client is a leading global CRO providing first excellent support to the Pharmaceutical and Biotechnology industries. This company have a great portfolio of work within Drug Safety and now due to workload require a driven Project Manager to join the safety team in the Maidenhead office.
- Regulatory Affairs Manager EMEA - OTC
Regulatory Affairs Manager EMEA - OTC
Employment type: Permanent
Salary: Dependent upon experience, candidates considered with expectations circa £55,000 - £65,000
- Junior Project Manager / Study Management Associate - Pharma -
Junior Project Manager / Study Management Associate - Pharma - UK (Buckinghamshire) My client is a global Pharmaceutical company who are urgently looking for a Junior Project Manager / Study Management Associate to join their team on a 12 Month Contract. Ideally you will have a proven track record as a CRA / Senior CRA. Home office working is not possible and you must be site based in the Buckinghamshire office. ...
- Regulatory Affairs Manager
I exclusively recruiting for my client, a specialist consultancy company providing global Regulatory Affairs, Pharmacovigilance and Quality Assurance services, who are searching for a Regulatory Affairs Manager to head up their growing team.Their services cover medicines, medical devices, cosmetics and other borderline substances. Our clients include large, medium and small pharmaceutical companies located across the world.
- PV Officer
I am currently seeking a Pharmacovigilance Officer to join an exciting and rapidly expanding company based in the South East of England. This is a permanent role that has been created as a result of expansion.