Clinical Operations Subject Matter Expert - Change Management - FSP - Remote

TN United Kingdom; Uxbridge; Remote; GBP 70,000 - 90,000; Full time

Job summary

A leading company is seeking a Clinical Operations Subject Matter Expert to oversee change management for clinical trials. This remote position based in Uxbridge requires extensive experience in clinical operations and stakeholder management. The successful candidate will lead workstreams and collaborate with various partners to ensure effective training and solutions.

Qualifications

• Highly experienced clinical operations leader with experience in insourced and outsourced programs.
• Prior clinical trial management experience within a global clinical research/pharma/biotech organization.

Responsibilities

• Provide oversight and expertise to the change management team.
• Lead the Knowledge Transfer/Management workstream.
• Partner with SMEs to create a robust Training plan.

Skills

Communication

Stakeholder Management

Job description

Clinical Operations Subject Matter Expert - Change Management - FSP - Remote, Uxbridge

Client:

Parexel

Location:

Uxbridge, United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Reference:

94ac378f6d55

Job Views:

2

Posted:

17.05.2025

Expiry Date:

01.07.2025

Job Description:

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

Parexel is currently seeking an experienced Clinical Operations Leader to support one of our key sponsors in the EMEA through a change management plan. This is a 12-month fixed-term contract.

As a SME for Clinical Operations, you will be responsible for providing in-depth oversight and clinical operations expertise to the change management team and various workstreams.

Key responsibilities include:

• Bring experience and knowledge from a Trial Management perspective on outsourced studies
• Contribute actively towards the workstreams
• Lead the Knowledge Transfer/Management workstream
• Partner with SMEs and other partners to create a robust Training plan
• Act as a key partner with CROs and internal SMEs, especially Study Leadership, Country SMEs, Reg Affairs, and Global Clinical Supplies, for identifying and building solutions

Requirements for this role:

• Highly experienced clinical operations leader with demonstrable experience working within insourced and outsourced programs
• Excellent communication and stakeholder management skills
• Prior clinical trial management experience within a global clinical research/pharma/biotech organization

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Created on 17/05/2025 by TN United Kingdom