Program Clinical Delivery Lead (all genders)

TN United Kingdom; Greater London; On-site; GBP 60,000 - 100,000; Full time

Job summary

An established industry player is seeking a Program Clinical Delivery Lead to oversee the quality and delivery of clinical studies. This role involves providing strategic direction and operational oversight for clinical research activities while promoting data-driven planning. The ideal candidate will have extensive experience in clinical operations, particularly in phases I-IV, and possess a strong background in medical or life sciences. Join a dynamic team focused on innovative research and make a significant impact in the field of clinical development. If you are passionate about driving excellence in clinical trials, this is the perfect opportunity for you.

Qualifications

• 12+ years of clinical research experience with expertise in Phases I-IV.
• Strong knowledge of clinical development principles and regulatory environments.

Responsibilities

• Lead delivery and quality of various clinical studies and research activities.
• Drive proactive risk-based site oversight and ensure timely issue resolution.

Skills

Adaptability / Flexibility

Critical Thinking

Strong Communication Skills

Analytical Skills

Business Partnering

Clinical Trials Knowledge

Influencing Skills

Strategic Thinking

Therapeutic Area Knowledge

Education

Medical or Life Sciences degree

Equivalent qualification in clinical research

Job description

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Program Clinical Delivery Lead (all genders), Feltham

Client:

Location:

Feltham, United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Reference:

8cc1c067b32b

Job Views:

4

Posted:

18.04.2025

Expiry Date:

02.06.2025

Job Description:

This position can be filled within Europe.

Your role:

1. Accountable for the delivery and quality of Phase I-IV, Epidemiology and Real World Evidence Company Sponsored Studies; Collaborative Research Studies; Investigator Sponsored Studies, Early Access Programs and other research activities.
2. Provide leadership, strategic direction and operational oversight for Clinical Site Lead (CSL) and/or Clinical Research Manager (CRM) activities across assigned program(s)/study(ies).
3. Serve as the operational delivery expert for the program(s)/study(ies) and promote data-driven, realistic planning at the site and study level.
4. Drive delivery-focused accountability and ownership amongst key external (CRO) and internal partners.
5. Facilitate identification and implementation of operational excellence strategies.
6. Drive proactive risk-based site oversight/study management practices and quality risk oversight and management.
7. Ensure timely and appropriate escalation of trends, issues and risks.
8. Promote solution-oriented thinking and issue resolution at the country/study/program team level.
9. Support program/product/study-specific onboarding for new CDPC team members.
10. Provide link between CSLs/CRMs and Global functions.
11. Lead regular calls with CSLs/CRMs working on study and/or other activities.
12. Participate in Investigator/Study Coordinator Meetings.
13. Represent the CSL group at the Clinical Operations Team (COT)/Clinical Trial Team (CTT).
14. Consolidate data-driven, CSL assessment of country and site selection proposals.
15. Lead activities with internal and external stakeholders to gather and integrate patient and physician insights.
16. Design country start-up strategy in consultation with the Start-up Solutions Team.
17. Design patient and site centric recruitment and retention strategies.
18. Oversee service providers to ensure successful implementation within agreed timelines, budget, and quality.
19. Establish monitoring strategy, including management of identified risks.
20. Utilise site performance and quality data analytics to drive proactive, risk-based site oversight practices.
21. Develop, implement and follow up on robust Site Oversight Plans.
22. Identify trends and issues within/across assigned study(ies).
23. Oversee Company Sponsored Studies, Collaborative Research Studies and Investigator Sponsored Studies.
24. Act as the global operations lead for Early Access activities.
25. Participate in GMA/Launch/Brand Team meetings.
26. Review program level CML Dashboard and Finance Tool on a monthly basis.

Who you are:

1. Medical or Life Sciences degree in a clinical research related discipline or equivalent.
2. Clinical operations experience – ideally across Phases (I-IV).
3. Expert knowledge of clinical development principles and regulatory environment.
4. Oncology and/or Neurology and/or Immunology TA experience desired.
5. Extensive (12+ years) professional and project management experience in clinical research.

Job specific Competencies and Skills:

1. Adaptability / Flexibility
2. Critical Thinking
3. Strong Communication Skills
4. Analytical Skills
5. Business Partnering
6. Clinical Trials Knowledge
7. Influencing Skills
8. Strategic Thinking
9. Therapeutic Area Knowledge

Position may require domestic/international travel up to 20% of time.

Please note that if you are NOT a passport holder of the country for the vacancy you might need a work permit.

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Created on 18/04/2025 by TN United Kingdom