Senior Clinical Trials Contracts Specialist in Reading

Senior Clinical Trials Contracts Specialist in Reading

Reading Full-Time 40000 - 50000 Β£ / year (est.) No working from home possible
IQVIA

At a Glance

  • Tasks: Manage contracts and grants for clinical trials while ensuring compliance with regulations.
  • Company: Join IQVIA, a leader in healthcare data and analytics.
  • Benefits: Competitive salary, health benefits, and opportunities for professional growth.
  • Other info: Exciting role in a fast-paced environment with career advancement potential.
  • Why this job: Make a difference in clinical research and work with a dynamic team.
  • Qualifications: Bachelor's Degree or equivalent experience with strong legal and negotiation skills.

The predicted salary is between 40000 - 50000 Β£ per year.

IQVIA is seeking a full-time contracting specialist located in Reading, UK. The successful candidate will develop and coordinate investigator grants, manage contract language, and ensure overall contracting efficiency in compliance with regulatory standards.

Ideal applicants should possess:

  • A Bachelor's Degree or equivalent experience
  • Strong legal and negotiating skills
  • A thorough understanding of clinical trial management

Senior Clinical Trials Contracts Specialist in Reading employer: IQVIA

IQVIA is an exceptional employer that fosters a collaborative and innovative work culture, making it an ideal place for professionals in the clinical trials field. Located in Reading, UK, employees benefit from a supportive environment that prioritises professional growth and development, alongside competitive compensation and comprehensive benefits. With a focus on compliance and efficiency, IQVIA empowers its team members to make meaningful contributions to the advancement of healthcare.

IQVIA

Contact Details:

IQVIA Recruitment Team

We think you need these skills to ace Senior Clinical Trials Contracts Specialist in Reading

Contract Management
Regulatory Compliance
Legal Skills
Negotiation Skills
Clinical Trial Management
Project Coordination
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