Senior RWE Expert
- Hiring from
- United Kingdom
- Work type
- Remote
- Posted
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We are recruiting a Senior RWE Expert to join a leading Pharmaceutical company on an initial 12 month contract. As the Senior RWE Expert you will be responsible for designing and delivering Real World Evidence programmes focused on women of childbearing age and other special patient populations, including older people and children.
This role will shape evidence that informs R&D, supports external healthcare decisions and strengthens understanding of disease. Your work will help patients, regulators, policymakers, payers and prescribers make better-informed decisions, with a particular focus on maternal and infant health.
This role offer fully remote working in the UK (You must have the right to work in the UK without sponsorship)
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Senior Real World Evidence Expert will be varied however the key duties and responsibilities are as follows:
1. As the Senior RWE Expert, you will shape asset level evidence strategy and tactical plans alongside the relevant strategy lead. You will identify evidence gaps across epidemiology, natural history, disease burden, care pathways and unmet need, while developing disease specific real world data infrastructure for special patient populations.
2. As the Senior RWE Expert, you will deliver global studies on time and within budget, from study concepts and protocols through statistical analysis plans, governance, quality control and milestone reporting. You will lead complex primary and secondary data studies, represent real world evidence on primary data collection teams, support local study teams and resolve operational challenges with external vendors, medical experts and analytical colleagues.
3. As the Senior RWE Expert, you will generate evidence addressing comparative effectiveness, long-term and patient-centred outcomes, background safety rates, drug utilisation and early post-launch experience. You will contribute to regulatory safety and effectiveness commitments, post-marketing surveillance, external control arms, hybrid designs, joint clinical assessment evidence needs and the data requirements of managed-entry programmes and value-based contracts.
4. As the Senior RWE Expert, you will interpret findings and communicate their implications through presentations, abstracts, posters and manuscripts. As the Senior Real World Evidence Expert, you will work with evidence synthesis, health economics, health technology assessment and pharmacovigilance colleagues to define evidence needs, defend scientifically sound methods and explore new data sources, advanced analytics, machine learning and artificial intelligence.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Senior Real World Evidence Expert we are looking to identify the following on your profile and past history:
1. Relevant degree in Epidemiology or Outcomes Research.
2. Extensive global or regional experience conceptualising and delivering real world evidence (RWE) studies using primary and secondary data within the pharmaceutical industry, a consultancy, CRO or Biotech organisation. Experience covering fertility, preterm birth, obstetric conditions, pregnancy, lactation or neonatal health, and/or innovative study designs, would be valuable.
3. A working knowledge and practical experience with rigorous quantitative research methods, cross-functional and cross-cultural collaboration, and translating findings into strategic recommendations and scientific communications. You will bring strong written and spoken English, confident presentation skills, scientific curiosity, adaptability and a commitment to maternal and infant health.
Key Words: Real World Evidence / Epidemiology / Pharmacoepidemiology / Outcomes Research / Maternal Health / Special Patient Populations / Secondary Data Studies / Comparative Effectiveness / Regulatory Evidence / Advanced Analytics / RWE / Epidemiologist / Primary Data / Secondary Data / US Claims Data / UK CPRD / Biotechnology / Biotech / Clinical / CRO / Pharma / Pharmaceutical
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
