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

Parexel International

United Kingdom

Remote

GBP 70,000 - 90,000

Full time

Yesterday
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Job summary

A leading company in the clinical research sector is seeking an experienced Clinical Operations Leader for a 12-month fixed-term contract. The role involves oversight of clinical operations, leading workstreams, and collaborating with various stakeholders to ensure effective change management. Ideal candidates will have a strong background in clinical trial management and excellent communication skills.

Qualifications

  • Highly experienced clinical operations leader professional.
  • Prior clinical trial management experience within a global clinical research/pharma/biotech organisation.

Responsibilities

  • Provide oversight and clinical operations 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

Education

BSc
Ms

Job description

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.

Working as a SME for Clinical Operationsyou will be responsible for providing in depth oversight and clinical operations expertise to the change management team and various workstreams.

Some specifics about this advertised role

  • Bring experience and knowledge from 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 esp. Study Leadership, Country SMEs, Reg Affairs, Global Clinical Supplies for identifying and building solutions

Here are a few requirements specific to this advertised role.

  • Highly experienced clinical operations leader professional 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 organisation
  • BSc, Ms or equivalent

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