Enable job alerts via email!

Freelance Director of Pharmacovigilance

JR United Kingdom

United Kingdom

Remote

GBP 125,000 - 150,000

Full time

14 days ago

Boost your interview chances

Create a job specific, tailored resume for higher success rate.

Job summary

An established industry player is seeking a Freelance Director of Pharmacovigilance to lead drug safety initiatives. This impactful role involves overseeing pharmacovigilance operations, ensuring compliance with regulatory standards, and developing comprehensive drug safety strategies. The ideal candidate will possess extensive experience in the field, strong analytical skills, and a proven track record in managing multiple projects. Join a collaborative and dynamic environment where your expertise will contribute to the safety of life-changing medications. This position offers a flexible remote working arrangement for a 6-month contract.

Qualifications

  • Extensive experience in pharmacovigilance and drug safety.
  • Strong understanding of regulatory requirements and industry standards.

Responsibilities

  • Oversee pharmacovigilance operations and ensure regulatory adherence.
  • Develop drug safety strategies and risk management plans.
  • Analyze safety data to identify risks and recommend actions.

Skills

Pharmacovigilance
Drug Safety
Regulatory Compliance
Analytical Skills
Problem-Solving

Education

Advanced degree in life sciences
Pharmacy degree

Job description

Social network you want to login/join with:

Freelance Director of Pharmacovigilance, united kingdom

col-narrow-left

Client:

AL Solutions

Location:
Job Category:

Other

-

EU work permit required:

Yes

col-narrow-right

Job Views:

6

Posted:

26.04.2025

Expiry Date:

10.06.2025

col-wide

Job Description:

Freelance Director of Pharmacovigilance/Drug Safety

We are seeking a highly skilled Director of Pharmacovigilance/Drug Safety for a 6-month freelance contract based in the UK. This role involves leading and managing all aspects of pharmacovigilance activities to ensure the safety and compliance of pharmaceutical products.

About the Company: This Clinical stage biotech, is looking to commercial their first product this year. The company fosters a collaborative and dynamic work environment. Your expertise will contribute to the development and safety of life-changing medications.

Key Responsibilities:

  • Oversee pharmacovigilance operations and ensure adherence to regulatory requirements.
  • Develop and implement comprehensive drug safety strategies and risk management plans.
  • Analyze safety data to identify potential risks and recommend appropriate actions.
  • Collaborate with cross-functional teams to maintain high standards of drug safety.
  • Provide expert guidance on pharmacovigilance processes and industry best practices.

Requirements:

  • Must be based in the UK, and be able to work without sponsorship
  • Advanced degree in life sciences, pharmacy, or a related field.
  • Extensive experience in pharmacovigilance and drug safety, preferably in a leadership role.
  • Strong understanding of regulatory requirements and industry standards.
  • Excellent analytical and problem-solving skills.
  • Ability to work independently and manage multiple projects simultaneously.
  • Duration: 6 months
  • Location: Remote
  • Hourly Rate - £100ph

If you have a proven track record in pharmacovigilance and drug safety, we invite you to apply for this impactful role. Join this team and contribute to the safety of pharmaceutical products globally.

Get your free, confidential resume review.
or drag and drop a PDF, DOC, DOCX, ODT, or PAGES file up to 5MB.