You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success.
We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires.
Your ideas influence the way we work, and your voice matters here.
As an essential part of our team, you help us deliver the medical innovation that patients are desperate for.
Join us and build your future here.
Review internal data and external literature to obtain a background understanding of Premier Research experience, country specific treatment patterns, available medications and competitive studies/market for disease areas to support Request For Proposal (RFP)
Design protocol specific site-level electronic feasibility questionnaires to collect metrics-based data, collate responses and analyse data to provide regularly updated summary report to proposal team for review
Compile the data into a report based on available data, together with the study team, make a recommendation on country selection, type of sites, numbers of sites, number of patients per country and recruitment timelines for inclusion in the proposal
Identify key information to be collated from local Study Start-Up Associates to support country strategy development
Write up medical informatics results and recommendations on strategic patient recruitment plan for inclusion in proposals and/or feasibility reports and bid defense slides
Undertake scientific literature reviews in collaboration with the medical strategist to understand treatment patterns, guidelines, standards of care and available medications for therapeutic disease areas within sponsor areas of focus.
Identify patient sources and flow, i.e. diagnosis, referral and treatment/care pathways in each country, to support the proposal bid and ultimately the project delivery post award.
Use computer-based models to project patient recruitment in studies, tailored to protocol design and country/site distribution
What We Are Searching For:
Minimum undergraduate degree in a clinical, biological, scientific, or health-related field, preferred postgraduate degree (MSc, MPhil or PhD) in a clinical, biological, scientific, or health-related field.
2+ years’ experience in a global Feasibility/Informatics related role required.
Prior clinical trials support or pharmaceutical industry experience is required.
Experience using external Clinical Trial Databases (e.g. Citeline) is highly desirable.
Excellent verbal and written English communication and presentation skills, demonstrating credibility in customer-facing situations.
