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Regulatory Affairs Strategist

Proclinical Staffing

Greater London

Hybrid

GBP 60,000 - 80,000

Full time

4 days ago
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Job summary

A leading pharmaceutical company in Greater London seeks a Regulatory Affairs Strategist for a maternity cover contract. You will develop and implement regulatory strategies for European markets, ensure compliance with regulations, and collaborate with various teams. The role requires strong knowledge of regulatory frameworks, experience with submissions, and excellent communication skills. This hybrid position begins in mid-January, offering a compelling opportunity to contribute to healthcare innovation.

Qualifications

  • Strong knowledge of European regulatory frameworks and guidelines.
  • Experience in preparing and managing regulatory submissions.
  • Ability to work effectively in a hybrid environment.

Responsibilities

  • Develop and implement regulatory strategies for European markets.
  • Ensure compliance with applicable regulatory requirements.
  • Collaborate with cross-functional teams to support product development.

Skills

Knowledge of European regulatory frameworks
Experience in regulatory submissions
Excellent communication skills
Collaboration skills
Organizational skills
Job description

Help bring science to life and join a leading pharmaceutical company to play a key role in regulatory strategy that drives healthcare innovation!

Proclinical is seeking a Regulatory Affairs Strategist for a maternity cover contract starting mid-January. This role involves contributing to regulatory strategies and ensuring compliance with European regulations. The position offers a hybrid working arrangement and requires timely availability to meet the start date.

Responsibilities
  • Develop and implement regulatory strategies for European markets.
  • Ensure compliance with applicable regulatory requirements and guidelines.
  • Collaborate with cross-functional teams to support product development and approval processes.
  • Prepare and review regulatory documentation and submissions.
  • Provide strategic advice on regulatory matters to internal stakeholders.
  • Monitor changes in regulatory environments and assess their impact on projects.
Key Skills and Requirements
  • Strong knowledge of European regulatory frameworks and guidelines.
  • Experience in preparing and managing regulatory submissions.
  • Excellent communication and collaboration skills.
  • Ability to work effectively in a hybrid environment.
  • Detail-oriented with strong organizational skills.

If you are having difficulty in applying or if you have any questions, please contact Peter Duvall at p.duvall@proclinical.com.

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

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