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- Tasks: Lead and oversee clinical studies, ensuring quality and timely delivery.
- Company: Join a dynamic team focused on innovative clinical research in Feltham.
- Benefits: Enjoy flexible working options and opportunities for professional growth.
- Why this job: Make a real impact in healthcare while collaborating with diverse teams.
- Qualifications: Medical or Life Sciences degree with 12+ years in clinical research required.
- Other info: Position may involve travel; work permit needed for non-residents.
The predicted salary is between 54000 - 84000 £ per year.
This position can be filled within Europe.
Your role:
- 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.
- 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).
- Serve as the operational delivery expert for the program(s)/study(ies) and promote data-driven, realistic planning at the site and study level.
- Drive delivery-focused accountability and ownership amongst key external (CRO) and internal partners.
- Facilitate identification and implementation of operational excellence strategies.
- Drive proactive risk-based site oversight/study management practices and quality risk oversight and management.
- Ensure timely and appropriate escalation of trends, issues and risks.
- Promote solution-oriented thinking and issue resolution at the country/study/program team level.
- Support program/product/study-specific onboarding for new CDPC team members.
- Provide link between CSLs/CRMs and Global functions.
- Lead regular calls with CSLs/CRMs working on study and/or other activities.
- Participate in Investigator/Study Coordinator Meetings.
- Represent the CSL group at the Clinical Operations Team (COT)/Clinical Trial Team (CTT).
- Consolidate data-driven, CSL assessment of country and site selection proposals.
- Lead activities with internal and external stakeholders to gather and integrate patient and physician insights.
- Design country start-up strategy in consultation with the Start-up Solutions Team.
- Design patient and site centric recruitment and retention strategies.
- Oversee service providers to ensure successful implementation within agreed timelines, budget, and quality.
- Establish monitoring strategy, including management of identified risks.
- Utilise site performance and quality data analytics to drive proactive, risk-based site oversight practices.
- Develop, implement and follow up on robust Site Oversight Plans.
- Identify trends and issues within/across assigned study(ies).
- Oversee Company Sponsored Studies, Collaborative Research Studies and Investigator Sponsored Studies.
- Act as the global operations lead for Early Access activities.
- Participate in GMA/Launch/Brand Team meetings.
- Review program level CML Dashboard and Finance Tool on a monthly basis.
Who you are:
- Medical or Life Sciences degree in a clinical research related discipline or equivalent.
- Clinical operations experience – ideally across Phases (I-IV).
- Expert knowledge of clinical development principles and regulatory environment.
- Oncology and/or Neurology and/or Immunology TA experience desired.
- Extensive (12+ years) professional and project management experience in clinical research.
Job specific Competencies and Skills:
- Adaptability / Flexibility
- Critical Thinking
- Strong Communication Skills
- Analytical Skills
- Business Partnering
- Clinical Trials Knowledge
- Influencing Skills
- Strategic Thinking
- 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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Program Clinical Delivery Lead (all genders) employer: TN United Kingdom
Contact Detail:
TN United Kingdom Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Program Clinical Delivery Lead (all genders)
✨Tip Number 1
Familiarise yourself with the latest trends and developments in clinical research, particularly in Oncology, Neurology, and Immunology. This knowledge will not only help you during interviews but also demonstrate your commitment to staying updated in your field.
✨Tip Number 2
Network with professionals in the clinical research community, especially those who have experience in Phase I-IV studies. Attend relevant conferences or webinars to connect with potential colleagues and learn about their experiences.
✨Tip Number 3
Prepare to discuss specific examples of how you've driven operational excellence in previous roles. Highlight your experience with risk management and data-driven decision-making, as these are crucial for the Program Clinical Delivery Lead position.
✨Tip Number 4
Research StudySmarter's values and mission to align your responses during the interview. Showing that you understand our culture and how you can contribute will set you apart from other candidates.
We think you need these skills to ace Program Clinical Delivery Lead (all genders)
Some tips for your application 🫡
Understand the Role: Thoroughly read the job description for the Program Clinical Delivery Lead position. Make sure you understand the responsibilities and required skills, especially in clinical research and project management.
Tailor Your CV: Customise your CV to highlight relevant experience in clinical operations, particularly across Phases I-IV. Emphasise any specific knowledge in Oncology, Neurology, or Immunology, as well as your project management experience.
Craft a Compelling Cover Letter: Write a cover letter that connects your background to the job requirements. Use specific examples from your past experiences to demonstrate your adaptability, critical thinking, and strong communication skills.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects attention to detail, which is crucial in clinical research roles.
How to prepare for a job interview at TN United Kingdom
✨Showcase Your Clinical Expertise
Make sure to highlight your extensive experience in clinical operations, especially across Phases I-IV. Be prepared to discuss specific projects you've managed and how your expertise aligns with the requirements of the Program Clinical Delivery Lead role.
✨Demonstrate Leadership Skills
Since this role involves providing leadership and strategic direction, be ready to share examples of how you've successfully led teams or projects in the past. Discuss your approach to fostering collaboration and driving accountability among team members and external partners.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving abilities and critical thinking skills. Prepare to discuss how you would handle potential risks or issues in a clinical study, showcasing your proactive and solution-oriented mindset.
✨Understand the Therapeutic Areas
Familiarise yourself with the latest developments in Oncology, Neurology, and Immunology, as these are desired areas of expertise. Being knowledgeable about current trends and challenges in these fields will demonstrate your commitment and readiness for the role.
