Medical Director – Clinical Development – Nephrology
Pharma-Partners is working with a fast-growing Global CRO to help increase the medical expertise of the business in certain key therapeutic specialties. This organisation has expanded organically and has an operational office presence in multiple countries across the globe. A large proportion of the clinical research projects they manage for clinical-stage biotech sponsors are in rare diseases, across different therapy areas, which means their medical leaders are truly involved in high-science and innovation.
A Medical Director in this business is involved “top to bottom” activities, and will find you operating in a flatter more agile structure compared to larger CRO environments where decision-making can sometimes be less rapid.
Acting as the therapeutic subject matter expert for global and regional clinical trials cross different phases, you will provide on-going medical expertise for:
- Clinical trial design and site selection
- Clinical Study Report creation (CSRs)
- Trial feasibility assessments
- Management of Medical Information
- Regulatory document assessment and submission
- Supporting Business Development teams, staying involved in proposal meetings and sponsor engagement
- Management of drug safety activities and medical monitoring responsibility
Candidate requirements include:
- Qualified physician (local country registration required)
- Recognised specialist in Nephrology essential (Board Certified or equivalent)
- Experience in clinical research ideally in pharmaceutical medicine, however clinical academics considering a move into industry will be considered
- Medical monitoring experience and an understanding of global drug safety best practice
- Someone who enjoys a busy and fast-paced role
- Good experience managing multiple projects and challenges at one time
To apply for this position please use the “Easy Apply” option or feel free to send your CV directly to the Pharma-Partners team via email info@pharma-partners.co.uk