채용
(Senior) Principal - Clinical Outcome Assessment Science - Multiple locations in Europe - Hybrid/Home-based

(Senior) Principal - Clinical Outcome Assessment Science - Multiple locations in Europe - Hybrid/Home-based
London; Amsterdam; Madrid; Paris; Basel; Berlin
·
On-site
·
Full-time
·
3w ago
This opportunity is available in multiple locations in Europe (within European Union, Switzerland and the UK). Please don't hesitate to apply even if you don't find your preferred location on the location list. The role can be hybrid or home-based. Please submit your CV in English.
IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics, and human ingenuity to drive healthcare forward.
The Patient Centered Solutions team(PCS)
The PCS team 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?
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Become part of a recognized global leader in patient-focused research
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Keep growing with an organization that encourages and invests in continuous professional and personal development
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Apply your business and leadership skills in an entrepreneurial and multi-disciplinary team
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Continue challenging yourself by addressing the toughest client issues, working across multiple geographies and solutions in a dynamic and crucial field for the industry
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Make a difference to patients by enabling the successful approval or launch of new treatments with features that are truly patient-centric
Responsibilities
The Principal/ Senior Principal Clinical Outcome Assessment (COA) Endpoint Strategy serves as the senior scientific authority for COA endpoint strategy, endpoint development, COA regulatory strategy, and COA instrument science in client engagement and project delivery. This role brings deep expertise in COA measurement science to differentiate client solutions through expert-driven, highly insightful endpoint 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. Key responsibilities include:
Client Strategy Leadership & Scientific Differentiation
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Develop COA endpoint strategies across clinical development programs, including primary and key secondary endpoint positioning in consulting projects.
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Bring senior COA expertise into client meetings, workshops, and strategic discussions.
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Differentiate proposals and client solutions through expert-driven COA strategy narratives.
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Translate emerging scientific and regulatory expectations into actionable client recommendations.
Regulatory-Grade Endpoint Strategy & FDA Engagement
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Advise sponsors on development and justification of COA endpoint strategies for regulatory interactions.
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Support preparation for and participation in FDA meetings as the COA subject matter expert.
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Guide sponsors on evidence expectations, context of use, and fit-for-purpose COA strategies.
COA Instrument Development Leadership
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Provide senior scientific leadership in the development of new COA instruments from concept to validation-ready tools.
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Lead and advise on drafting and refinement of COA instrument items, response options, recall periods, and scoring approaches.
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Oversee qualitative research activities supporting content validity, including concept elicitation and cognitive interviewing.
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Ensure new COA instruments are patient-centered, scientifically robust, and fit-for-purpose for clinical and regulatory use.
Internal SME Oversight & Quality Assurance
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Serve as subject matter expert overseeing internal project teams executing COA strategy and development work.
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Review and approve key scientific deliverables to ensure quality, rigor, and alignment with best practices.
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Mentor and coach COA scientists and consultants, supporting capability development across the organization.
Business Development & Practice Growth
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Support business development through proposal leadership, solution design, and client presentations.
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Contribute to the evolution of COA strategy methodologies, frameworks, and reusable assets.
External Scientific Leadership & Visibility
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Maintain a strong external profile through publications, conference presentations, and scientific collaborations.
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Represent IQVIA as a recognized expert in COA science and endpoint strategy.
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Contribute to academic teaching, advisory boards, or industry working groups where appropriate.
Essential experience, skills and education required
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Deep expertise across COA types (PRO, ObsRO, ClinRO, PerfO) and their application in clinical research.
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Extensive experience developing COA endpoint strategies across multiple therapeutic areas.
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Hands-on experience developing new COA instruments, including item writing and qualitative validation.
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Strong experience supporting FDA-facing endpoint strategy and regulatory interactions.
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Proven ability to lead, mentor, and oversee multidisciplinary scientific teams.
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Excellent scientific writing, presentation, and stakeholder engagement skills.
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Advanced degree (PhD, MD, PharmD, DrPH, MSc) in a relevant scientific discipline strongly preferred.
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Strong publication record and recognized credibility in outcomes research or COA measurement science.
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Well-developed written and verbal communication skills including presentations, chairing meetings, external conference presentations, workshop facilitation, business and report writing.
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An entrepreneurial nature and interest in developing new client offerings and solutions and in building the capability to deliver the same.
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.
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IQVIA 소개

IQVIA
PublicIQVIA Holdings, Inc. is an American company based in Durham, North Carolina, focused on health information technology and clinical research.
10,001+
직원 수
Durham
본사 위치
$17B
기업 가치
리뷰
3.6
10개 리뷰
워라밸
3.8
보상
2.5
문화
4.0
커리어
3.2
경영진
2.8
65%
친구에게 추천
장점
Good work-life balance
Supportive team and collaborative environment
Flexible hours and good benefits
단점
Compensation below industry standards
High workload and overwhelming at times
Poor management communication and organization
연봉 정보
51개 데이터
Junior/L3
Senior/L5
Junior/L3 · Analyst
2개 리포트
$107,910
총 연봉
기본급
$93,834
주식
-
보너스
-
$97,750
$118,068
면접 경험
3개 면접
난이도
3.0
/ 5
소요 기간
14-28주
경험
긍정 0%
보통 33%
부정 67%
면접 과정
1
Application Review
2
HR Screen
3
Hiring Manager Interview
4
Technical Manager Interview
5
Executive/GM Interview
6
Offer
자주 나오는 질문
Behavioral/STAR
Case Study
Technical Knowledge
Past Experience
Culture Fit
뉴스 & 버즈
Whittier Trust Co. Has $4.04 Million Stake in IQVIA Holdings Inc. $IQV - MarketBeat
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4d ago
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