Senior Drug Safety Scientist/Great role for PSUR writer/Bucks




Job Type: Full Time / Flexi Time

Job Flexibility: Medium Flexibility

Location Requirement: UK – S. England

General Area Of Expertise Required: Proj. Man – Admin

Salary: Commission Based

Job Description: Pharmacovigilance Scientist – excellent senior role for PSUR writer

Nonstop is working closely with an interesting organisation in recruiting a Pharmacovigilance Scientist. The company will provide you with very strong experience and have one of the best training programmes in the industry. You will be given the opportunity to utilise your experience and aid the company by working with some of the biggest names in the industry.

As Pharmacovigilance Scientist, some of responsibilities:

1. Writing of Periodic reports as required (PSURs, ASRs), narrative writing 2. Process and review adverse event information utilising the product safety
database:
3. Produce project specific process guidelines – Work with clients to devise, produce and maintain working procedures to ensure PV regulatory compliance.
4. Accounting of time – Ensure itemised tracking of time spent on specific projects.
5. Devise and produce literature search strategies and review literature – 6. Collaboration with medical staff, team members and clients concerning safety issues.
7. Ensure implementation of Standard Operating Procedures:
8. Regulatory Intelligence:

Successful candidates will have previous experience with Pharmacovigilance which must include varied PSUR writing experience.

For a confidential discussion and to find out more information about this role please contact Harriet Maidman on 0207 234 0550 or by e-mail to h.maidman@nonstop-pharma.com



Contact Details: Harriet Maidman

Business Details:

Nonstop Recruitment

0207 234 0550

h.maidman@nonstop-pharma.com

Applicants should send a cover letter and CV to the email supplied with the position title and any reference in the subject line.

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