Global Scientific Lead - Clinical Outcome Assessment (COA) Strategy Consulting - Multiple locat[...] in London

Global Scientific Lead - Clinical Outcome Assessment (COA) Strategy Consulting - Multiple locat[...] in London

London Full-Time 80000 - 100000 £ / year (est.) Home office (partial)
IQVIA

At a Glance

  • Tasks: Lead innovative research to enhance patient experiences in clinical outcomes.
  • Company: Join a global leader in patient-focused research with a dynamic team.
  • Benefits: Enjoy hybrid work options, continuous development, and competitive compensation.
  • Other info: Opportunity for career growth in a supportive and entrepreneurial environment.
  • Why this job: Make a real difference in healthcare by shaping patient-centric treatment strategies.
  • Qualifications: Advanced degree and expertise in clinical outcome assessments required.

The predicted salary is between 80000 - 100000 £ per year.

Location: Multiple locations across the European Union, Switzerland, and the United Kingdom. The role can be hybrid or fully home‑based.

Patient Centered Solutions team (PCS) leads the industry in the science of measuring the patient experience. We pair strategic consulting expertise with technical scientific knowledge to design and execute scientifically rigorous research that incorporates the patient voice into the development and commercialization of new medicines. This research includes qualitative (e.g., patient interviews, focus groups), quantitative (e.g., clinical outcome assessments (COAs)/patient‑reported outcomes (PROs), preference research) and passive (e.g., digital health technology tools) approaches to understand patient, caregiver and physician experiences and expectations of disease and treatment.

Why join?

  • Become part of a recognized global leader in patient‑focused research
  • Keep growing with an organization that encourages and invests in continuous professional and personal development
  • Apply your business and leadership skills in an entrepreneurial and multi‑disciplinary team
  • Continue challenging yourself by addressing the toughest client issues, working across multiple geographies and solutions in a dynamic and crucial field for the industry
  • Make a difference to patients by enabling the successful approval or launch of new treatments with features that are truly patient‑centric

Responsibilities

The Global Scientific Lead for Clinical Outcome Assessment (COA) Endpoint Strategy serves as the senior scientific authority in the COA Consulting team within Patient Centered Solutions. This role brings deep expertise in COA measurement science and Patient Experience Data (PED) more broadly, to differentiate client solutions through expert‑driven, highly insightful endpoint and PED strategies. The role acts as a trusted advisor to pharmaceutical and biotechnology sponsors and represents IQVIA as an external scientific thought leader while ensuring internal scientific quality and best practices. The role provides organisational leadership for COA science through a combination of direct people management and influence by setting the standards and strategy for the scientific work of the consulting team.

People and organizational leadership

  • Serve as the global scientific lead for consulting activities, providing strategic oversight and leadership across the PCS consulting organization
  • Lead and develop talent through a combination of direct line management, broader mentoring, and active cultivation of scientific capabilities across the consulting team
  • Champion excellence in scientific outputs, driving consistency, quality, and innovation in clinical outcome assessment (COA) and PED‑related deliverables
  • Set and shape the long‑term vision and strategy for scientific activities within consulting, working in close partnership with senior leadership

Client Strategy Leadership & Scientific Differentiation

  • Develop COA endpoint and PED strategies across clinical development programs, including primary and key secondary endpoint positioning in consulting projects.
  • Bring senior COA and PED expertise into client meetings, workshops, and strategic discussions.
  • Differentiating proposals and client solutions through expert‑driven COA and PED strategy narratives.
  • Translate emerging scientific and regulatory expectations into actionable client recommendations.

Regulatory‑Grade Endpoint Strategy & FDA Engagement

  • Advise sponsors on development and justification of COA endpoint strategies for regulatory interactions.
  • Support preparation for and participation in FDA meetings as the COA subject matter expert.
  • Guide sponsors on evidence expectations, context of use, and fit‑for‑purpose COA strategies.

COA Instrument Development Leadership

  • Provide senior scientific leadership in the development of new COA instruments from concept to validation‑ready tools.
  • Lead and advise on drafting and refinement of COA instrument items, response options, recall periods, and scoring approaches.
  • Oversee qualitative research activities supporting content validity, including concept elicitation and cognitive interviewing.
  • Ensure new COA instruments are patient‑centered, scientifically robust, and fit‑for‑purpose for clinical and regulatory use.

Internal SME Oversight & Quality Assurance

  • Serve as subject matter expert overseeing internal project teams executing COA and PED strategy and development work.
  • Review and approve key scientific deliverables to ensure quality, rigor, and alignment with best practices.
  • Mentor and coach COA and PED scientists and consultants, supporting capability development across the organization.

Business Development & Practice Growth

  • Support business development through proposal leadership, solution design, and client presentations.
  • Contribute to the evolution of COA strategy and PED methodologies, frameworks, and reusable assets.

External Scientific Leadership & Visibility

  • Maintain a strong external profile through publications, conference presentations, and scientific collaborations.
  • Represent IQVIA as a recognized expert in COA science and endpoint strategy.
  • Contribute to academic teaching, advisory boards, or industry working groups where appropriate.

Essential experience, skills and education required

  • Deep expertise across COA types (PRO, ObsRO, ClinRO, PerfO) and their application in clinical research.
  • Extensive experience developing COA endpoint strategies across multiple therapeutic areas.
  • Hands‑on experience developing new COA instruments, including item writing and qualitative validation.
  • Strong experience supporting FDA‑facing endpoint strategy and regulatory interactions.
  • Broad experience across PED methodologies and application of PED by regulators, payers and other stakeholders desirable.
  • Proven ability to lead, mentor, and oversee multidisciplinary scientific teams.
  • Excellent scientific writing, presentation, and stakeholder engagement skills.
  • Advanced degree (PhD, MD, PharmD, DrPH, MSc) in a relevant scientific discipline strongly preferred.
  • Strong publication record and recognized credibility in outcomes research or COA measurement science.
  • Well‑developed written and verbal communication skills including presentations, chairing meetings, external conference presentations, workshop facilitation, business and report writing.
  • An entrepreneurial nature and interest in developing new client offerings and solutions and in building the capability to deliver the same.

EEO Minorities/Females/Protected Veterans/Disabled

Global Scientific Lead - Clinical Outcome Assessment (COA) Strategy Consulting - Multiple locat[...] in London employer: IQVIA

Join a leading global organisation that prioritises patient-focused research and fosters a culture of continuous professional development. With the flexibility of hybrid or fully remote work options across multiple locations in the EU, Switzerland, and the UK, you will be part of a dynamic team that values innovation and collaboration while making a meaningful impact on patient care through scientifically rigorous strategies. Embrace the opportunity to grow your career in a supportive environment that champions excellence and encourages you to challenge yourself in addressing complex client needs.

IQVIA

Contact Details:

IQVIA Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Global Scientific Lead - Clinical Outcome Assessment (COA) Strategy Consulting - Multiple locat[...] in London

Tip Number 1

Network like a pro! Reach out to people in the industry, attend relevant events, and connect with professionals on LinkedIn. You never know who might have the inside scoop on job openings or can refer you directly.

Tip Number 2

Prepare for interviews by researching the company and its culture. Understand their patient-centered approach and be ready to discuss how your skills align with their mission. Show them you’re not just another candidate!

Tip Number 3

Practice makes perfect! Conduct mock interviews with friends or mentors to refine your answers and boost your confidence. Focus on articulating your experience with COA strategies and how they can benefit potential clients.

Tip Number 4

Don’t forget to follow up after interviews! A simple thank-you email can leave a lasting impression and keep you top of mind. Plus, it shows your enthusiasm for the role and the company.

We think you need these skills to ace Global Scientific Lead - Clinical Outcome Assessment (COA) Strategy Consulting - Multiple locat[...] in London

Clinical Outcome Assessment (COA) expertise
Patient Experience Data (PED) knowledge
Qualitative research methods
Quantitative research methods
Regulatory interactions experience
FDA engagement skills
COA instrument development

Some tips for your application 🫡

Tailor Your Application:Make sure to customise your CV and cover letter for the Global Scientific Lead role. Highlight your expertise in COA measurement science and patient experience data, as these are key to standing out.

Showcase Your Experience:Don’t just list your qualifications; share specific examples of how you've developed COA strategies or led multidisciplinary teams. We want to see your impact and how you can contribute to our Patient Centered Solutions team.

Be Clear and Concise:When writing your application, keep it straightforward. Use clear language and avoid jargon where possible. This will help us understand your skills and experiences without getting lost in complex terminology.

Apply Through Our Website:We encourage you to submit your application directly through our website. It’s the best way to ensure your application gets into the right hands and shows your enthusiasm for joining our team!

How to prepare for a job interview at IQVIA

Know Your COA Inside Out

Make sure you have a solid understanding of Clinical Outcome Assessments (COAs) and Patient Experience Data (PED). Brush up on the different types of COAs, their applications in clinical research, and recent developments in the field. This will help you demonstrate your expertise and show that you're genuinely interested in the role.

Prepare for Client Strategy Discussions

Think about how you would approach client meetings and strategic discussions. Be ready to share examples of how you've differentiated proposals or solutions in the past. This will showcase your ability to bring senior COA and PED expertise into conversations and highlight your strategic thinking.

Showcase Your Leadership Skills

Since this role involves people management and mentoring, be prepared to discuss your leadership style and experiences. Share specific examples of how you've developed talent or driven excellence in scientific outputs. This will help the interviewers see you as a potential leader within their team.

Engage with Regulatory Insights

Familiarise yourself with regulatory expectations around COA endpoint strategies, especially regarding FDA interactions. Be ready to discuss how you've supported sponsors in these areas before. This will demonstrate your capability to guide clients through complex regulatory landscapes and reinforce your value as a subject matter expert.