Therapeutic Analytics Lead, Clinical Trial Strategy

Iqvia; Greater London; On-site; GBP 85,000 - 125,000; Full time

Job summary

IQVIA in London seeks a Therapeutic Analytics Lead to shape country, site and patient enrollment strategies for complex global trials. You will merge clinical trial expertise, data and strategic thinking to drive client recommendations for APAC opportunities, including China, collaborating with medical, strategy, business development and operations teams.

You will translate diverse data sources into clear insights, present strategies to clients and senior stakeholders, and mentor colleagues

Qualifications

• 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 related field, or equivalent experience.
• Strong understanding of clinical research, trial lifecycle and drug development.
• Experience interpreting data and informing decisions with evidence.
• Strong communication and presentation skills for senior stakeholders.

Responsibilities

• 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 countries, sites and enrollment approaches for study delivery.
• Translate data and 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 and senior stakeholders.
• Research therapeutic areas and trial environments to inform study strategy.
• Evaluate data to determine relevance of sources and insights for each opportunity.
• Serve as an SME for feasibility and planning tools and mentor colleagues.

Skills

Mandarin proficiency

English proficiency

Clinical research experience

Data interpretation

Presentation skills

Independent work

Education

Bachelor’s degree in healthcare or life sciences

Job description

Therapeutic Analytics Lead, Clinical Trial Strategy

Location: London, United Kingdom

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.