Clinical Study Manager

Anne-Dorthe Wilms; Manchester; On-site; GBP 40,000 - 60,000; Full time

Job summary

A leading early phase clinical trials company in Manchester is looking for a Clinical Study Manager. This role involves leading the execution of clinical studies, coordinating activities across all phases, and acting as the main point of contact for sponsors. The ideal candidate should possess strong organizational and communication skills. You'll benefit from a supportive team environment and excellent career growth opportunities.

Benefits

29 days annual leave plus bank holidays

Company pension scheme

Generous annual bonus

Healthcare plan

Free secure on-site parking

Qualifications

• Familiarity with clinical research, GCP, or regulatory guidelines is beneficial but not essential.

Responsibilities

• Coordinate and lead clinical trial activities across all phases.
• Act as the main point of contact for sponsors on enrolment and study queries.
• Ensure study procedures are followed in line with protocols and regulatory standards.
• Support site staff and CRAs during monitoring visits and data reviews.
• Help drive process improvements and maintain documentation quality.

Skills

Strong organizational skills

Strong communication skills

Proactive mindset

Ability to work independently

Ability to work in a team

Job description

Overview

Clinical Study Manager An exciting role to join a continually expanding early phase clinical trials company working with some of the most distinguished domestic and global pharmaceutical companies. We're offering a stimulating and rewarding career pathway for anyone looking to work within our busy clinical trials as a Clinical Study Manager to lead the day-to-day execution of clinical studies from start-up to close-out.

Responsibilities

• Coordinate and lead clinical trial activities across all phases
• Act as the main point of contact for sponsors on enrolment and study queries
• Ensure study procedures are followed in line with protocols and regulatory standards
• Support site staff and CRAs during monitoring visits and data reviews
• Help drive process improvements and maintain documentation quality

What We're Looking For

• Strong organizational and communication skills
• A proactive mindset and ability to work both independently and in a team
• Familiarity with clinical research, GCP, or regulatory guidelines is beneficial but not essential; full training will be provided

This is a fantastic opportunity to grow within a supportive clinical operations team and contribute to impactful research.

What We Offer

• 29 days annual leave plus bank holidays, increasing to 33 days after 5 years' service
• Company pension scheme
• Generous annual bonus and healthcare plan after qualifying period
• Free secure on-site parking
• Healthcare plan