Therapeutic Analytics Lead, Clinical Trial Strategy

IQVIA Inc; Greater London; On-site; GBP 90,000 - 130,000; Full time

Job summary

IQVIA is seeking an experienced Therapeutic Analytics Lead to join the Therapeutic Strategy & Insights team in London. You will blend clinical trial expertise, data, and strategic thinking to shape country, site and patient enrollment strategies for global studies.

Ideal candidates have Mandarin and English proficiency, 5+ years in clinical research, and a strong track record in data-informed decision making.

Qualifications

• 5+ years of experience in clinical research or clinical trials.
• Bachelor's degree in healthcare, life sciences, biological sciences or related discipline.
• Strong understanding of clinical research, lifecycle and drug development.
• Ability to interpret data and inform clinical or operational decisions.

Responsibilities

• Lead development of country, site and patient enrollment strategies for complex trials.
• Analyze clinical and operational data to identify enrollment approaches.
• Translate data and insights into actionable recommendations for clients and teams.
• Present strategies and supporting evidence in client meetings and bid defenses.
• Mentor colleagues and contribute to improvements in planning processes.

Skills

Mandarin

English

Clinical research

Data analysis

Stakeholder comms

Education

Bachelor's degree in healthcare/life sciences

Job description

London, United Kingdom

Full time

R1576853

We are looking for an experienced clinical research professional to join our Therapeutic Strategy & Insights team as a Therapeutic Analytics Lead.

You will combine clinical trial expertise, data and strategic thinking to develop country, site and patient enrollment strategies for complex global studies.

Working closely with medical, therapeutic strategy, business development and operational teams, you will turn multiple sources of data into clear recommendations and present them to clients and senior stakeholders.

This role will have a particular focus on supporting APAC opportunities, including China. Therefore, professional proficiency in both Mandarin and English is required.

What you’ll do

• Lead the development of country, site and patient enrollment strategies for complex clinical trial opportunities, including RFPs, early engagements and re-bids.
• Analyze multiple clinical and operational data sources to identify the countries, sites and enrollment approaches most likely to support successful study delivery.
• Translate complex data and clinical research insights into clear, actionable recommendations for clients and internal teams.
• Present strategies and supporting evidence during client meetings and bid defenses.
• Lead planning discussions with Medical Directors, Therapeutic Strategy Leads, Business Development, Clinical Operations and other senior stakeholders.
• Research therapeutic areas, treatment landscapes and clinical trial environments to inform study strategy.
• Use your clinical research experience to critically evaluate data and determine which sources and insights are most relevant to each opportunity.
• Serve as a subject-matter expert for relevant feasibility and planning tools.
• Mentor and support colleagues and contribute to improvements in planning processes and ways of working.
• Stay current with developments in clinical research and drug development.

What we’re looking for

Essential

• Professional proficiency in Mandarin and English, both written and spoken.
• At least 5 years of experience in clinical research or clinical trials.
• A bachelor's degree in healthcare, life sciences, biological sciences or a related discipline, or an equivalent combination of education and relevant experience.
• Strong understanding of clinical research, the clinical trial lifecycle and drug development.
• Experience interpreting data and using evidence to inform clinical or operational decisions.
• Strong communication and presentation skills, with the ability to work confidently with senior stakeholders and clients.
• Ability to work independently, prioritize multiple activities and operate effectively in a cross-functional, matrix environment.

Experience in one or more of the following would be particularly valuable:

• Clinical trial feasibility
• Country or site selection
• Patient enrollment planning or strategy
• Clinical project or study management
• Clinical operations
• Global or APAC clinical trials
• Client-facing work within a CRO, pharmaceutical or biotechnology environment

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

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