Study Start Up Specialist (FSP) - Istanbul
3 days left
- Experience Level
- Experienced (non-manager)
Permanent, full-time position. Dedicated to one prestigious sponsor.
1/2 days office-based Istanbul with option for 3/4 days home-based.
Sponsorship is not available.
Everything we do has the potential to impact patient lives, and our Site Activation Partners (SAP) take their work seriously, demonstrate empathy, and act with heart. They also perform with urgency, navigating our streamlined clinical operating model to drive effectiveness, reduce handoffs and increase employee, client, and site satisfaction.
As a SAP at Parexel, you will be joining a team with a wide variety of experiences and knowledge. We’re looking for people like you to take the initiative to do things better and smarter people who want to grow personally and professionally. We recognize and uphold the importance of all people, the way we do things, our quest for innovation, and most importantly, our patients.
The SAP is responsible for supporting operational activities related to site evaluation, activation, initiation, monitoring and close out for assigned investigator sites/studies to ensure compliance with study timelines and GCP standards.
Completion of critical information for site activation including Investigator Initiation Packages (IIP), confidentiality agreements, study contracts, clinical supply shipment information, payment information, IRB submission and status.
Skills and Education:
Experience in study activation and/or site management from a pharmaceutical / biotechnology or CRO environment.
EC submissions experience.
Demonstrated knowledge of global and local regulatory requirements
Demonstrated understanding of key operational elements of a clinical trial (e.g., study start-up, conduct, close-out activities, reporting.
Fluent in English and local language.
About ExecuPharm/Parexel FSP
A global provider of functional service solutions across a range of specialized disciplines for clinical development and biopharmaceutical product lifecycle support including clinical operations, biometrics, safety, regulatory, medical writing, and medical affairs.
For results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is the CRO trusted by life sciences companies to innovate keeping patients at the center of everything we do, and where an inclusive global community helps you be your best, transforming any career into a life-changing achievement.
For an immediate telephone interview please contact the job poster
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