12 Month - Local Trial Manager - FSP - Remote

Parexel; London; Remote; GBP 50,000 - 70,000; Full time

Job summary

Join Parexel as a Trial Manager on a 12-month contract in London, overseeing clinical trials' operational and scientific aspects. You will ensure trial compliance, manage budgets, and lead training. This role requires strong decision-making and analytical skills, ideal for candidates with substantial clinical research experience.

Qualifications

• Minimum 5+ years in clinical research with CRO, biotech, or pharma.
• 3-5 years leading end-to-end clinical trials.

Responsibilities

• Ensure trial compliance with GCP-ICH and local regulations.
• Manage trial budgets, ensuring financial oversight.
• Conduct trial-specific training for partners.

Skills

Decision-making

Analytical skills

Financial skills

Education

BSc/Ba degree

Job description

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12 Month - Local Trial Manager - FSP - Remote, London

Client: Parexel

Location: London, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Reference: ac45689326cd

Job Views: 4

Posted: 02.07.2025

Expiry Date: 16.08.2025

Job Description:

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

Parexel is recruiting an experienced Trial Lead/Manager for a 12-month fixed-term contract in the UK. This role is not open to Freelance or Independent Contractor applicants.

As a Trial Manager, you will oversee the operational and scientific aspects of clinical trials at the local level, contributing to project delivery through accurate planning and efficient execution, ensuring speed and value for patients and sites.

Key Responsibilities:

• Ensure trial compliance with GCP-ICH, local regulations, SOPs, and protocol by overseeing CRO and internal activities.
• Manage and review trial budgets, ensuring financial oversight and timely updates.
• Conduct trial-specific training for internal and external partners as per the Trial Training Plan.
• Coordinate operational feasibility and trial timelines, ensuring team alignment.
• Validate site selection and feasibility using data and local insights.
• Develop engagement and recruitment plans; collaborate on patient-facing documents; report feedback for trial improvements.
• Maintain oversight during trial conduct, ensuring adherence to GCP, regulations, SOPs, and risk mitigation.

About Parexel:

We support clinical studies across therapeutic areas, partnering with a diverse client base, from top-selling drugs to niche developments.

Our Values:

We seek professionals committed to patient well-being, working with heart.

Role Requirements:

• BSc/Ba degree required.
• Minimum 5+ years in clinical research with CRO, biotech, or pharma, across phases 1-4.
• 3-5 years leading end-to-end clinical trials.
• Strong decision-making, analytical, and financial skills.