Full-Time

Contracts Officer

Posted on 9/12/2025

Deadline 10/3/25
MHRA

MHRA

1,001-5,000 employees

Regulates medicines and medical devices

No salary listed

Watford, UK

Hybrid

Minimum of 8 days per month working on site, with potential to flex up to 12 days.

Category
Legal & Compliance (1)
Requirements
  • Experience in research contract drafting and negotiation
  • Professional business, legal or paralegal qualification
  • Communicating and Influencing
  • Making effective decisions
  • Team working
Responsibilities
  • Research Contract Management (inc review, drafting and negotiation)
  • Developing and maintaining stakeholder relationships
  • Clear communication
  • Document Control and traceability

MHRA is an executive non-departmental public body responsible to the Secretary of State for Environment, Food and Rural Affairs. Its purpose is to protect and improve England’s natural environment and to encourage people to enjoy and get involved in their surroundings. It carries out policy implementation, land stewardship, conservation funding, and public engagement through government-backed programs and partnerships with landowners, communities, and volunteers. Its goal is to safeguard natural spaces, biodiversity, and landscapes while inviting people to participate in caring for and enjoying the environment.

Company Size

1,001-5,000

Company Stage

N/A

Total Funding

N/A

Headquarters

London, United Kingdom

Founded

1989

Simplify Jobs

Simplify's Take

What believers are saying

  • Flexible wildlife licensing for infrastructure projects balances conservation with necessary development.
  • Evidence-based standards and partnerships target 30x30 nature recovery and species decline halt.
  • Green infrastructure integration through spatial planning delivers combined environmental and community benefits.

What critics are saying

  • 20% MHRA workforce reduction undermines regulatory capacity and clinical trial oversight.
  • Only five operational Approved Bodies create bottlenecks for Class III device conformity assessments.
  • Post-Brexit regulatory divergence forces UK medtech firms into separate UKCA marking processes.

What makes MHRA unique

  • MHRA independently regulates UK medicines, vaccines, and medical devices post-Brexit.
  • Three-year Strategy for Improving Safety Communications transforms patient and healthcare professional engagement.
  • New regulations effective April 28, 2026 align UK clinical trial oversight standards.

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Benefits

Flexible Work Hours

Hybrid Work Options

Remote Work Options

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