Senior Manager Clinical Study Lead (Hematology)

Regeneron Pharmaceuticals, Inc; Cambridge; On-site; GBP 70,000 - 90,000; Full time

Job summary

A leading biotechnology firm is seeking a Senior Manager Clinical Study Lead in Cambridge. This onsite role focuses on executing global clinical trials, overseeing study timelines and budgets, and ensuring compliance. Candidates should have at least 8 years of experience in clinical trial operations, strong leadership skills, and a Bachelor’s degree. Exceptional interpersonal and problem-solving abilities are essential. Apply if you are proactive and can influence various stakeholders.

Qualifications

• Minimum 8 years of relevant experience in clinical trial operations.
• Strong communication and problem-solving skills.
• Ability to manage timelines, budgets, and compliance.

Responsibilities

• Lead global execution of complex clinical trials.
• Manage study teams and oversee documentation.
• Conduct risk assessments and manage patient recruitment.

Skills

Interpersonal skills

Leadership

Clinical trial operations

Communication

Problem-solving

Stakeholder influence

Vendor management

Knowledge of ICH/GCP

Education

Bachelor’s degree

Tools

Trial management systems

MS Office

Job description

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Senior Manager Clinical Study Lead (Hematology), Cambridge

Location: Cambridge, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Reference: b2f1b7ab9392

Job Views: 16

Posted: 12.08.2025

Expiry Date: 26.09.2025

Job Description:

This role is an onsite position in one of our office locations. Fully remote is not eligible.

The Senior Clinical Study Lead (CSL) is responsible for the global execution of complex clinical trials, from study design to close-out. The role requires independent operation, accountability for study timelines, budgets, and compliance with SOPs and ICH/GCP guidelines. It involves leadership of study teams, oversight of study documentation, vendor management, budget and timeline management, risk assessment, site evaluation, patient recruitment, data monitoring, and study close-out activities. The role also includes supervising staff and contributing to process improvements and study reports.

This role may be for you if you have:

• Exceptional interpersonal & leadership skills
• Advanced expertise in clinical trial operations and strategic guidance
• Strong communication and problem-solving skills
• Proactive, disciplined, and deadline-oriented
• Ability to influence stakeholders and manage vendors
• Knowledge of industry trends, ICH/GCP, and regulatory requirements
• Experience with trial management systems and MS Office applications
• Extensive global trial operations experience
• Bachelor’s degree and minimum 8 years of relevant experience