Jobs at Parexel
Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.
Local Study Associate Director - FSP
Job ID R0000029748 , TurkeyParexel FSP is hiring an Associate Clinical Study Director to join us on a
permanent full-time, 3 days office based.
If you’re driven by the potential of science to create meaningful change and eager to explore your capabilities, join us.
Dedicated to a single sponsor in BioPharma, who is revolutionizing healthcare by harnessing the power of science to benefit people, society, and the planet. Turkey is a vital part of their global network, hosting colleagues from every life sciences value chain segment. Their science-driven approach aims to transform healthcare and improve patient outcomes while fulfilling a purpose-led role in society.
As an Associate Study Director, you will lead Local Study Teams(LST) at the country level to deliver clinical studies according to agreed resources, budget, and timelines complying with procedural documents, international guidelines, and relevant local regulations. In addition to leading LST(s), ) may perform site monitoring as needed to support the flexible capacity model.
Responsible for ensuring that sites are identified, site qualifications performed, set up, initiated, monitored, closed and documentation archived. Overall responsibility for the study commitments within the country, for timely delivery of data to required quality as per SMA. Lead Local Study Team(s) consisting of CRAs, start-up specialists, and study administrator(s).
Essential Requirements
Bachelor’s degree in a related discipline, preferably in life science, or equivalent qualification.
At least 1 year experience as a Clinical Trial Leader or Project leader.
Minimum 3 years of experience in Development Operations (CRA, SrCRA) or other related fields (Medical Affairs-led or Academic-led studies).
Experience in oncology trials.
Good knowledge of international guidelines ICHGCP as well as relevant local regulations.
Proven ability to lead and motivate cross-functional teams to deliver clinical trials according to or ahead of time plan, budget, and with required quality.
Excellent project management skills.
We offer exceptional financial rewards, training, and development. Expect exciting professional challenges but with a healthy work/life balance. We value your welfare just as highly as that of our patients.
Apply today!
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