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Clinical Site Manager | Hybrid | Cambridge

SoCode Limited

Cambridge

Hybrid

GBP 40,000 - 70,000

Full time

2 days ago
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Job summary

An innovative BioTech company in Cambridge is seeking a Clinical Site Manager to lead imaging studies and enhance clinical trials for patients with complex diseases. This hybrid role offers flexibility, allowing up to four remote days a week, and emphasizes strong career development opportunities. You will be responsible for managing clinical sites, ensuring compliance with regulatory standards, and maintaining project milestones. If you have a passion for advancing medical technology and experience in clinical trial management, this position is a fantastic opportunity to make a real impact in the field.

Benefits

Competitive salary + share options
Flexible and hybrid working policy
25 days annual leave + bank holidays
Private medical insurance
Medical Cash Plan
Death in Service benefit
Pension scheme
Professional development opportunities
Co-working space access

Qualifications

  • 2+ years managing clinical trial sites, ideally in imaging.
  • Strong understanding of clinical imaging workflows.

Responsibilities

  • Lead site qualification and training activities.
  • Manage clinical sites through the full project lifecycle.

Skills

Clinical trial management
Imaging workflows
Stakeholder management
Problem-solving
Communication skills

Education

Bachelor's degree in Life Sciences

Tools

GCP certification
QMS (ISO 9001/13485)

Job description

Overview:
We're working with a cutting-edge BioTech company based in Cambridge, focused on using AI and imaging to transform clinical trials for patients with complex diseases. They're looking for a Clinical Site Manager with experience in imaging studies to join their team.
This is a hybrid role (up to 4 remote days/week) with lots of flexibility and strong career development opportunities.

Key Responsibilities:

  1. Lead site qualification, training, and scanner onboarding activities.
  2. Manage clinical sites through the full project lifecycle, acting as the main point of contact.
  3. Perform imaging QC in line with SOPs and regulatory standards.
  4. Track site and project milestones, ensuring accurate documentation and reporting.
  5. Support project kick-offs, bid defences, and continuous process improvements.
  6. Maintain compliance with GCP, ISO27001, and relevant data privacy regulations.

Experience Required:

  1. 2+ years' experience managing clinical trial sites, ideally within an imaging CRO or Core Imaging Lab.
  2. Strong understanding of clinical imaging workflows and site coordination.
  3. Up-to-date GCP certification and familiarity with working under QMS (ISO 9001/13485 desirable).
  4. Excellent communication skills, proactive problem-solving approach, and stakeholder management experience.
  5. Bachelor's degree (or equivalent) in Life Sciences.

Benefits:

  1. Competitive salary + share options
  2. Flexible and hybrid working policy
  3. 25 days annual leave + bank holidays
  4. Private medical insurance (including pre-existing conditions)
  5. Medical Cash Plan & Death in Service benefit
  6. Pension scheme
  7. Professional development and academic collaboration opportunities
  8. Co-working space access
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