Study Manager - Pharmacology, Cardiovascular Toxicology

Recruiter
Clinical Professionals
Location
Cambridgeshire
Salary
£23,000 - £32,000
Posted
13 Nov 2017
Closes
16 Nov 2017
Sector
Healthcare
Contract Type
Permanent
Hours
Full Time
Study Manager - Pharmacology, Cardiovascular Toxicology
Permanent
£23,000 - £32,000
Cambridgeshire

Are you interested in working for a globally renowned CRO that specialises in biopharmaceutical drugs & vaccine development for human & animal health, using your in-depth skill-set & knowledge in project management and cardiovascular toxicology within a small-team at the forefront of drug discovery and development?

Our client is looking to bring on board a Study Manager to their Cardiovscular Toxicology research team, where you`ll be responsible for managing a variety of studies to clients` requirements & specifications, as well as being the Monitoring Toxicologist on relevant studies.

Duties/Responisibilities:
- Manage the initiation, day-to-day running, completion, reporting & archiving of assigned studies
- Act as the main point of contact for clients/customers to establish and deliver on agreed specifications
- Recording, collating and reporting on the cardiovascular effects of new drugs on large animals

Requirements/Experience:
- Previous experience as a study director or project manager within the pharmaceutical industry or a Cardiovascular Animal Health background
- Previous client interaction experience within a CRO environment
- Experience in and knowledge of Cardiovascular/Arrhythmia
- Educated to at least BSc, ideally MSc or PhD in a relevant discipline
- Strong data analysis skills
- Knowledge and experience with safety pharmacology & regulatory guidelines
- Current eligibility to work in the UK

Study Manager, Project Manager, Project Director, Study Director, Animal Health, Toxicology, Toxicologist, Monitoring Toxicologist, Pharmacology, Cardiovascular, Arrhythmia, safety pharmacology, regulatory guidelines