- Regulatory Affairs Manager CMC
Manager, Regulatory Affairs CMC – Emerging MarketsThe CompanyMy client, a leading Biotech company, with a global presence and highly reputable market presence, is looking for a Manager within their Regulatory Team. This company is rapidly growing year on year and producing products that are changing the world. With more and more MA applications happening each year, their expansion is set to continue exponentially. ...
- Pharmacovigilance Manager
This is a brilliant new opportunity which has arisen with a large pharmaceutical company based in Maidenhead, Berkshire.They are looking for a strong PV professional with at least five years of previous experience.
- Senior Pharmacovigilance Scientist
Brand new Senior Pharmacovigilance Scientist opportunity with a leading pharmaceutical company!
Senior Pharmacovigilance Scientist
Location: Alderley Park, Cheshire
6 month contract with competitive daily rate or opportunity to be permanently employed by Clinical Professionals with attractive salary and benefits package
Offers exposure to early phase and oncology studies
- Senior Regulatory Affairs Manager (m/w)
Senior Regulatory Affairs Manager (m/w)Office-based in MunichJob Description:? Responsible for the preparation of regulatory submissions in compliance with global requirements. These may include IND and related amendments, CTAs and related amendments, and global safety and annual reports.? Support meetings with Regulatory Authorities including requesting agency meetings and publishing of associated briefing documents. ...
- Senior Regulatory Affairs Manager
My client is a leading research-based global pharmaceutical company, and they focus on the discovery, development, manufacturing and marketing of a large variety of top-quality pharmaceutical products.
- Regulatory Specialist
Regulatory Specialist West London – JOB SUMMARY:My client a leading global organization with offices worldwide is recruiting for a Regulatory Specialist to manage assigned projects in accordance with their Regulatory requirement and SOPs.Location: BerkshireRESPONSIBILITIES -Responsible for oversight of regulatory submissions for assigned projects/countries/sites, which may include completion of submissions or notifications, as required. ...
- Regulatory Affairs Senior Associate
Regulatory Affairs Senior AssociateMy client, a leading Regulatory Affairs consultancy, is looking for an experienced candidate to join them as a Senior Associate. My client works with over 400 global pharmaceutical and biotechnology customers and they need a strong candidate to help advise these key industry giants. ...
- Regulatory Manager
Regulatory Affairs Manager - CMCMy client, a very well-known and respected consultancy, is looking for an experienced Regulatory affairs professional to join their company. This professional will have 6+years working in CMC, predominantly in post approval. Candidates must be eligible to work in the UK. ...
- Regulatory Affairs Consultant
Regulatory Affairs Consultant –CMCThe companyThis company is a top 5 global CRO with a large and ever growing consulting arm. This company is global company with over 10,000 employees across all continents. They are a company that help their clients get medicines into the hands of those who need them most. They offer scientific know how, industry expertise and an outstanding environment to learn and grow. ...
- Regulatory Affairs and Pharmacovigilance Executive
The UK Bausch + Lomb team is currently recruiting for a Regulatory Affairs and Pharmacovigilance Executive to join our Kingston office. Reporting into the Regulatory Affairs Manager, you will be responsible for coordinating the day-to-day management of the pharmacovigilance local system in the UK and Ireland (Vision Care, Pharma, Surgical and GPSS franchises) and ensuring local compliance with applicable Regulations and Corporate policies (local and global).