- Qualified Person for Pharmacovigilance / QPPV contractor
We are recruiting for a Qualified Person for Pharmacovigilance (QPPV) for a minimum contract of 6 months with a competitive hourly rate!!
- Manager Medical Writing
A very dynamic international CRO is looking for an experienced Medical writer Manager able to develop all medical writers & ensure the highest level of delivery for key projects related to Pharmacovigilance, clinical development, regulatory submissions, and all other deliverables.
- Regulatory Affairs Manager CMC
Manager, Regulatory Affairs CMC – Emerging Markets
My 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. ...
- Associate Director Regulatory Affairs
Associate Director, Regulatory Affairs - Cambridgeshire
A lot of regulatory professionals will be lucky if they get within touching distance of a MAA in a 4/5 year period. My client is expecting to push 1 or 2 out a year. Be part of something big and help it become even bigger!
My client, a leading Biotech company with global coverage and highly reputable market presence, is looking for a Manager within their Pharmacovigilance team. ...
- Regulatory Affairs Manager (m/w)
Regulatory Affairs Manager (m/w)
Office-based in Munich
? Regulatory Affairs (RA): Preparation of regulatory submissions, mainly CTA, for investigational products
in line with European and local requirements
? Management of submissions for CTA’s incl. ...
- 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. They have recently created this role in London for an experienced senior manager to join their team in order to sustain compliance and aid the company's Marketing Authorisations.
- Regulatory Affairs Manager CTA – West London
Regulatory Affairs Manager CTA - West London
My client, a dynamic company which is globally recognised as an extremely reputable company has an urgent opening for a Regulatory Affairs Manager CTA. The successful candidate will join the EU Regulatory Team based in the UK.
- Senior Regulatory Affairs Consultant
Senior Regulatory Affairs Consultant –Regulatory – Home based
This 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. ...
- Medical Advisor & PV Contract
This role will provide support to the QPPV Pharma in managing strategic functions of the QPPV Office. This will include:
* Oversight of pharmacovigilance systems and business pharmacovigilance compliance.
* Management of the Detailed Description of Pharmacovigilance Systems (DDPS) for updating and variation applications.
* Review and commenting on EU-RMPs and FDA REMS.
* Support to Health Authority Inspections and internal audits for local operating companies and global
- Medical Advisor (Pharmacovigilance)
Here is a chance to join one of the most globally known pharmaceutical organisations, who are looking to hire a Medical Advisor (Pharmacovigilance) based in Hertfordshire. This job is at a top 10 pharmaceutical company that works across a range of industries from medical devices to pharmaceutical and consumer goods, operating in over 60 countries. This is a contract job for 6 months with possible extension. ...