Clinical Trial Manager (LSAD) - UK, Remote - FSP

Parexel; London; Remote; GBP 50,000 - 75,000; Full time

Job summary

Parexel is seeking a Local Study Associate Director to drive clinical trials in the UK. In this role, you will lead study teams, manage budgets, and ensure regulatory compliance, contributing to vital clinical studies for global biotech and pharmaceutical clients. Join a supportive environment that values career development and work-life balance.

Qualifications

• Minimum 3 years' experience in local clinical trials.
• Strong organizational, interpersonal, and problem-solving skills.
• Experience with submissions to RA and EC.

Responsibilities

• Responsible for delivering clinical study components according to resources, budget, timelines, and regulations.
• Leads and optimizes local study teams, ensuring compliance with procedures and regulations.
• Prepares country financial agreements and manages the study budget.

Skills

Leadership

Team Motivation

Problem Solving

Organizational Skills

Interpersonal Skills

Job description

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Clinical Trial Manager (LSAD) - UK, Remote - FSP, London

Client: Parexel

Location: London, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Reference:

25b1f418a099

Job Views:

3

Posted:

16.07.2025

Expiry Date:

30.08.2025

Job Description:

When our values align, there's no limit to what we can achieve.

Parexel is seeking a Local Study Associate Director (Clinical Operations Leader) to join us in the UK. You will be assigned to a key sponsor in the region.

Working as a LSAD at Parexel FSP offers long-term job security and prospects. We undertake vital clinical studies for global biotechs and Pharma top 50, with an exciting pipeline of work.

Opportunities in clinical operations, project management, line management, or other fields await you.

Our LSADs work from home, supporting regional studies. Our mantra: ‘Manageable sites, manageable protocols’. Expect professional challenges in inspiring studies, with time for your outside life.

Role specifics

Dedicated to one client.

Responsible at country level for delivering clinical study components according to resources, budget, timelines, and regulations.

Prepares country financial Study Management Agreement (fSMA) and maintains the study budget.

Leads and optimizes local study teams, ensuring compliance with procedures and regulations.

Prepares and manages informed consent forms and translations, ensuring compliance.

Submits applications/documents to EC/IRB at startup and throughout the study.

Role requirements

Minimum 3 years' experience in local clinical trials.

Proven leadership and team motivation skills.

Experience and willingness to monitor oncology trials, if needed.

Experience with submissions to RA and EC.

Ability to collaborate with study functions for smooth delivery.

Strong organizational, interpersonal, and problem-solving skills.

Good knowledge of clinical research, trial phases, GCP/ICH, and local laws.

We value our people and offer a supportive environment with career development opportunities.

About Parexel

Parexel supports clinical studies across various therapeutic areas, partnering with a broad client base.

We have contributed to the trials of many top-selling drugs and niche developments vital to patients' well-being.

You will be a key member of our team.