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Parexel is seeking an experienced Clinical Project Leader/Senior Project Leader to oversee global biotech studies. The role focuses on delivering projects on time and on budget with high quality, while aligning with ICH GCP standards.
This position requires strong leadership in cross-functional teams and deep clinical research insight to meet client expectations and drive outcomes. Preferred candidates will have oncology exposure and broader therapeutic area knowledge, with a proactive,
When our values align, theres no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Parexel is in the business of improving the worlds health. We do this by providing a suite of biopharmaceutical services that help clients across the world transform scientific discoveries into new treatments. We believe in our values, _ Patients First, Quality, Respect, Empowerment & Accountability. _
We are currently looking to recruit an experienced _ Project Leader or Senior Project Leader _ to lead project delivery to our _ Biotech clients _ and their projects on a global level. You will ideally have Therapeutic Area expertise in a combination of the following: Oncology plus any of the following Dermatology, Women’s Health, Neurology, Rare Disease or Radiopharmaceuticals.
This position is available in the following EMEA locations - _ UK, Ireland, Poland, Romania, Spain, Hungary, Lithuania _ and we offer fully remote (country stipulated) home based working.
As the _ Clinical _ Project Leader or Senior Project Leader (Clinical Project Manager) you will actively lead the Parexel and client teams by combining your deep clinical research experience with insight into client pressures in order to develop the right solution for the client.
You will provide overall cross-functional leadership of our clinical trials and studies as well as the project teams to achieve operational excellence and deliver projects on time, to budget, with the highest quality as well as being compliant with ICH GCP to meet client expectations.
Bachelors degree or equivalent level of education (Science or Medical related field preferred) or proven substantial clinical project management experience.
Advanced degree desirable.
Strong previous CRO experience and understanding of _ Phase I, II-III clinical trial project management _ with demonstrable _ project leadership _ skills are essential.
In-depth knowledge of the Therapeutic Areas due to our current resource needs: Oncology is essential plus any of the following Dermatology, Women’s Health, Neurology, Rare Disease, Radiopharmaceuticals are desirable.
Strong command of written and spoken English language is essential.
Strong _ financial management _ and _ client relationship _ skills as well as involvement with _ bid defense activities _ are essential.
Applications from candidates with pharma experience may also be considered.
- Familiarity with standard business and eClinical systems used in Clinical Research is desirable.
ICH and GCP regulations in relevant geographies.
Solid clinical knowledge and understanding of clinical research and protocol design.
In return we will be able to offer you a structured career pathway and development within the role including awareness and understanding of the industry. Your hard work will be rewarded with a competitive salary, bonus, (car allowance is country specific) and a benefits package including holiday, pension and other leading-edge benefits that you would expect with a company of this type.
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