Clinical Site Manager | Hybrid | Cambridge

TieTalent; Cambridge; Hybrid; GBP 40,000 - 70,000; Full time

Job summary

An innovative BioTech company in Cambridge is seeking a Clinical Site Manager to lead imaging studies and enhance clinical trial processes. This hybrid role offers flexibility, allowing up to four remote days each week, and emphasizes career development within a cutting-edge environment. As the main point of contact for clinical sites, you will manage project lifecycles, ensuring compliance with regulatory standards and maintaining high-quality documentation. Join a team dedicated to transforming clinical trials through advanced AI and imaging technologies, and contribute to impactful projects that make a difference for patients with complex diseases.

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 throughout the project lifecycle.

Skills

Clinical trial management

Imaging studies

Communication skills

Problem-solving

Stakeholder management

Education

Bachelor’s degree in Life Sciences

Tools

GCP certification

QMS (ISO 9001/13485)

Job description

This job offer is presented to you through one of our partners. Click on "Show interest" to be redirected.

Clinical Site Manager | Hybrid | Cambridge

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