Senior Regulatory Scientist in Bracknell

Senior Regulatory Scientist in Bracknell

Bracknell Full-Time 60000 - 80000 £ / year (est.) No working from home possible
Proclinical Staffing

At a Glance

  • Tasks: Lead regulatory strategies for innovative diabetes treatments and ensure compliance with local regulations.
  • Company: Proclinical, a dynamic company focused on cutting-edge healthcare solutions.
  • Benefits: Impactful role with opportunities for mentorship and professional growth.
  • Other info: Collaborative environment that values diversity and continuous improvement.
  • Why this job: Make a real difference in patients' lives by bringing new therapies to market.
  • Qualifications: Advanced scientific degree and strong knowledge of regulatory procedures required.

The predicted salary is between 60000 - 80000 £ per year.

Be the strategic force behind bringing cutting-edge diabetes treatments to market. Proclinical is seeking a Senior Regulatory Scientist to provide strategic regulatory leadership and oversight for assigned products within the diabetes therapy area. In this role, you will be responsible for aligning local regulatory strategies with global objectives, ensuring compliance with regional regulations, and leading interactions with regulatory authorities. This position offers an opportunity to make a significant impact on product development, approval, and lifecycle management in a dynamic and collaborative environment.

Responsibilities:

  • Develop and implement local regulatory strategies aligned with global plans for assigned products.
  • Lead the preparation, submission, and approval of high-quality regulatory documents, including local labeling and packaging.
  • Manage relationships and lead interactions with regional regulatory authorities, influencing outcomes to support business objectives.
  • Provide regulatory expertise to cross‑functional teams, ensuring compliance with local and regional requirements.
  • Monitor and interpret evolving regulatory guidelines, initiating changes as needed to maintain compliance.
  • Support clinical trial registration needs for local patients in the region.
  • Collaborate with global regulatory leads to address development and regulatory challenges.
  • Participate in regional meetings to align regulatory strategies with commercial and medical needs.
  • Mentor and guide team members, fostering an inclusive and innovative work environment.
  • Contribute to continuous improvement initiatives to enhance efficiency and productivity.

Key Skills and Requirements:

  • Advanced scientific degree (e.g., PhD, MD, PharmD) or equivalent experience in regulatory affairs or drug development.
  • Strong knowledge of local and regional regulatory procedures and practices.
  • Demonstrated ability to navigate complex regulatory environments and manage risk effectively.
  • Excellent written, verbal, and presentation communication skills.
  • Proven negotiation and influencing abilities.
  • Attention to detail and a commitment to quality.
  • Experience in medical device or in‑vitro diagnostics regulatory activities is a plus.
  • Ability to work collaboratively across diverse teams and embrace equity and inclusion.

Senior Regulatory Scientist in Bracknell employer: Proclinical Staffing

Proclinical is an exceptional employer that champions innovation and collaboration in the healthcare sector, particularly in diabetes treatment. With a strong commitment to employee growth, we offer mentorship opportunities and a dynamic work culture that values inclusivity and continuous improvement. Join us in making a meaningful impact on patient lives while enjoying the benefits of working in a supportive environment that aligns local regulatory strategies with global objectives.

Proclinical Staffing

Contact Details:

Proclinical Staffing Recruitment Team

We think you need these skills to ace Senior Regulatory Scientist in Bracknell

Regulatory Strategy Development
Regulatory Compliance
Regulatory Document Preparation
Interaction with Regulatory Authorities
Cross-Functional Team Collaboration
Monitoring Regulatory Guidelines
Clinical Trial Registration