At a Glance
- Tasks: Lead and manage Phase IV and Real-World Evidence studies across multiple countries.
- Company: Join a leading global pharmaceutical organisation with a collaborative culture.
- Benefits: Fully remote role offering flexibility, autonomy, and competitive salary.
- Other info: Gain exposure to scientific publications and medical strategy initiatives.
- Why this job: Make a real impact on patient outcomes through high-impact evidence generation.
- Qualifications: Degree in Life Sciences and 4+ years of study management experience required.
The predicted salary is between 60000 - 80000 £ per year.
We're partnering with a leading global pharmaceutical organization to find an experienced RWE Study Manager to lead the delivery of Phase IV and Real-World Evidence (RWE) studies across multiple countries. This is a fantastic opportunity to take ownership of multinational evidence-generation studies, working closely with Medical Affairs, CROs, investigators, and external partners from study start-up through to final reporting.
What you'll be doing:
- Lead the planning, execution, and delivery of Phase IV and RWE studies
- Manage study timelines, budgets, resources, risks, and key milestones
- Oversee CROs, vendors, sites, and external research partners throughout the study lifecycle
- Ensure compliance with GCP, GPP, regulatory requirements, SOPs, and data privacy standards
- Partner cross-functionally with Medical Affairs, Epidemiology, Biostatistics, Regulatory Affairs, Pharmacovigilance, Market Access, and Commercial teams
What we're looking for:
- Degree in Life Sciences, Epidemiology, Public Health, Pharmacy, or a related field
- 4+ years of Study Management experience within clinical research or pharmaceutical settings
- Experience managing Phase IV, observational, non-interventional, registry, or RWE studies internationally
- Strong project management, stakeholder management, vendor oversight, and risk management capabilities
- Knowledge of real-world data, post-marketing research methodologies, and pharmacovigilance requirements
Why this opportunity?
- Lead high-impact studies that contribute to evidence generation and patient outcomes
- Work within a highly collaborative and cross-functional global environment
- Gain exposure to scientific publications, congress presentations, and medical strategy initiatives
- Take ownership of complex multinational studies from start-up to final reporting
- Fully remote position with flexibility and autonomy
Interested or know someone who could be a fit? Feel free to reach out directly or apply confidentially!
RWE Study Manager employer: Meet Life Sciences
As a Market Access Consultant with our client, you will be part of a dynamic team that values innovation and collaboration in the evolving healthcare landscape. The company offers a supportive work culture with opportunities for professional growth, including mentoring junior team members and leading impactful projects. With competitive compensation, hybrid working options, and comprehensive benefits, this role provides a meaningful opportunity to contribute to the expansion of European Value & Access capabilities while enjoying a fulfilling work-life balance.
