Associate Director – Global Study Management - Poland
In continued support to one of our global Pharma clients, I am looking to speak with clinical project managers with experience of managing global study studies, ideally in the field of Oncology drug development.
This is an opportunity to join a leading pharmaceutical company in an Associate Director level role where you bring not only your clinical project management skills but also build on the leadership skills that you may have.
Candidates need to live in either Warsaw or Krakow region to make occasional visits to the company office(s).
Reporting to the Senior Study Director, you will be helping to lead a team of study managers by providing guidance towards success clinical study delivery.
Working across a range of often complex and cutting-edge clinical trials, you will be putting your excellent clinical project management skills in place as you work with both external stakeholders (Vendors/CROs, KOLs, labs etc.) as well as internal stakeholders and cross-functional teams (Data Management, Biometrics, Regulatory etc.).
In leading this study team, you will be making sure that studies stay on-track according to time and budget, be the main point of contact with the CRO for any outsourced studies and maintain the general oversight of the CRO/Vendor in tandem with the level or service and timelines agreed.
Experience of managing study budgets and input towards financial forecasting will be desirable.
Your experience within Clinical Operations will ideally include measuring the study performance against planned study milestones.
If you have strong, global clinical project management experience and some team leaderships skills, then this Associate Director role with a global pharma company will be an excellent career opportunity.
Get in touch with me – Simon Penrose – on +44 (0) 1293 584 300 or email firstname.lastname@example.org to discuss this position and your experience in more detail.
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