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An exciting opportunity has arisen with a market leading CRO who are actively looking for a Pharmacovigilance Project Manager. This opportunity would best suit someone with extensive experience within Drug Safety and who are looking to take that next step in an organisation which is experiencing rapid but sustainable growth.
- 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
- Regulatory Affairs Specialist
Exciting opportunity with a global pharmaceutical company for a Regulatory Affairs Specialist - highly competitive package available!!
- Senior Regulatory Affairs Specialist
Looking to advance your career? An exciting opportunity for a Senior Regulatory Affairs Specialist required for post marketing role - a permanent position with a global pharma company. Highly competitive salary offered!!
- Senior Associate Regulatory Affairs (Clinical Trials) Contract
Contract opportunity: Minimum 12 month contract position for a Senior Associate Regulatory Affairs within Clinical Trials to start ASAP with a Global pharma company!
- 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 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 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. ...
- Principle Consultant Regulatory Affairs
Principle Consultant Regulatory Affairs - IDMPThe 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. ...
- Global Expedited Reporting Manager- manage projects not people - central London- Can come from drug safety background
To apply for this Global Expedited Reporting Manager please call Julie Cooper on 07951 082482 or alternatively please send your CV to :firstname.lastname@example.org