- Senior Specialist, Regulatory Compliance (Late Stage) - UK - Home Based
We are currently seeking a Senior Specialist, Regulatory Compliance (Late Stage) to join our company, inVentiv Health Clinical. You will become a member of our inVentiv Health Clinical’ Late Stage Department to reflect the unique characteristics of our Late Stage Team and help world class companies bridge the gap from development to commercialization.
- Regulatory Affairs Snr Manager / French speaking Switzerland / Global CMC Biotech role
Regulatory Affairs Snr Manager / French speaking Switzerland / Global CMC Biotech role.
My Client is a Global organization that develops, manufactures and markets products that save and sustain the lives of people. They have a varied product portfolio which includes pharmaceutical and biotechnology products. Their office in Switzerland is seeking a highly skilled CMC regulatory specialist to operate in a unique role. Contact me, Theo Moore , on +44 (0)207 801 3384.
- RA/QA Specialist-Varied Working Life-Medical Devices-Suisse
Our client are looking for a regulatory affairs and quality specialist to work on innovative and world leading medical devices. This is an exciting broad role which will lead to a varied working life. You will be working across both regulatory affairs and quality assurance, allowing to you gain invaluable expertise across the full product life cycle. We want to hear from you today if you have experience in both regulatory affairs and quality assurance from the medical device industry.
- Senior Clinical Trial Assistant (Senior Specialist, Late Stage) - Maidenhead - office based
We are currently seeking a Senior Clinical Trial Assistant (Senior Specialist, Late Stage) to join our company, inVentiv Health Clinical.
This is an exciting opportunity for an experienced CTA to act as client-facing Late Stage specialist lead for assigned studies, providing guidance and resolving issues as needed. With experience in QC of TMFs, you will be office based in the UK (Maidenhead).
- Senior Regulatory Country Lead
An internationally known biotechnology company has an opening for a Senior Regulatory Country Lead job at their Berkshire office. The company has a strong reputation for developing innovative therapies for neurological diseases and employs approximately 7,000 people worldwide. ...
- Regulatory & Start-Up Specialist (6 month contract) - Reading, UK
Planet Pharma is looking for a Regulatory & Start-Up Specialist to work for a global CRO in Reading on 6 month contract. Start ASAP!
- Study Start Up Lead, CRO, London
Seeking a study start up specialist for a permanent opportunity available at a leading global CRO. A great opportunity for a dynamic and enthusiastic professional looking for opportunities for career development and progression. This CRO stands out through its rate of growth and expertise in specialist therapeutic areas.
- Senior Clinical Trial Specialist - Wavre, Belgium
PAREXEL is looking for Senior Clinical Trial Specialist to join our team in Wavre, Belgium.
- Senior Feasibility Specialist – Greater London – Up to £37,000 – Top 10 Global CRO – Unrivalled progression opportunities
Senior Feasibility Specialist – Greater London – Up to £37,000 – Top 10 Global CRO – Unrivalled progression opportunities - Please contact Kelsey Stack on 07983525166 or email firstname.lastname@example.org if you would like to know more about this opportunity. This will be 100% confidential.
- Associate Director/Director /General Medicine Therapeutic Lead
A fantastic opportunity to working for an established health care service provider, dealing with a range of regulatory affairs responsibilities on European and Global level.