Clinical Study Services Director

SciPro; Cambridge; Hybrid; GBP 80,000 - 100,000; Full time

Job summary

A leading clinical research organization in Cambridge is seeking an experienced Clinical Study Services Director to oversee study start-up and management of multiple projects. You'll mentor teams, ensure compliance, and improve processes. Candidates should have at least 3 years in clinical research and project management experience. This role offers a competitive salary and flexible hybrid working arrangements.

Benefits

Competitive holiday allowance

Flexible hybrid working model

Enhanced pension contributions

Private medical insurance

Health and wellbeing cash plan

Life insurance

Annual personal development allowance

Qualifications

• At least 3 years' experience in clinical research, preferably in imaging or CRO environments.
• Project management experience within a clinical trials environment.
• Previous team management experience or ambition to move into leadership.

Responsibilities

• Lead and develop a team of Clinical Study Managers.
• Oversee study start-up and ongoing management activities.
• Act as Project Manager for designated studies when required.
• Partner with clients to align project delivery.

Skills

Team management

Clinical project management

Attention to detail

Regulatory compliance

Job description

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

Overview

SciPro are on the hunt for 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