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Clinical Study Services Director

SciPro
Posted a day ago, valid for 12 days
Location

Cambridge, Cambridgeshire CB21NT, England

Salary

£70,000 - £90,000 per annum

Contract type

Full Time

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Sonic Summary

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  • SciPro is seeking an experienced Clinical Study Services Director in London/Cambridge to manage study start-up and delivery across multiple clinical research projects.
  • The role requires at least 3 years of experience in clinical research, with project management experience within a clinical trials environment preferred.
  • Key responsibilities include leading a team of Clinical Study Managers, overseeing study management activities, and ensuring compliance with regulatory standards.
  • The position offers a competitive salary and benefits, including flexible hybrid working, enhanced pension contributions, and private medical insurance.
  • Ideal candidates will possess strong leadership skills and a proactive approach to problem-solving in clinical study environments.

Clinical Study Services Director, London/Cambridge, (phone number removed)

SciPro are on the hunt for an an experienced Clinical Study Services Director to take ownership of study start-up and delivery activities across multiple clinical research projects.

This leadership role is ideal for someone who enjoys building and mentoring teams, improving processes, and ensuring that studies run smoothly from initiation through to close-out.

You'll be the key link between internal teams, external partners, and clients - making sure that projects are delivered to a high standard, within timelines, and in full compliance with regulatory requirements.

What You'll Do

  • Lead and develop a team of Clinical Study Managers, providing guidance, support and performance management

  • Oversee study start-up and ongoing management activities, ensuring efficient delivery of projects

  • Act as Project Manager for designated studies when required

  • Partner with clients to understand project objectives and align delivery accordingly

  • Review and approve essential study documentation, ensuring accuracy and compliance

  • Promote continuous improvement by refining processes and standard operating procedures

  • Ensure all activities meet Good Clinical Practice (GCP) standards and relevant regulatory frameworks

What You'll Bring

  • At least 3 years' experience in clinical research (experience in imaging, CRO or core lab settings is an advantage)

  • Project management experience within a clinical trials environment

  • Previous team management experience or the ambition to move into leadership

  • A proactive, solutions-focused approach with high attention to detail

Why Join Us

  • Competitive holiday allowance

  • Flexible hybrid working model

  • Enhanced pension contributions

  • Private medical insurance (with family cover included)

  • Health and wellbeing cash plan

  • Life insurance

  • Annual personal development allowance

If you're interested in finding out more and meet the above requirements, click apply now!

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SonicJobs' Terms & Conditions and Privacy Policy also apply.