Safety & PV Specialist I - Literature review Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization
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
Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated
Summary of Responsibilities: To complete Other duties/activities as assigned by study management team, but not limited to: Manage clinical systems and access management. Maintain study databases (CTMS, IWRS, EDC, etc.) Support study team in e-TMF management activities.
Safety & PV Specialist 1 - Clinical Trial case processing Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development
Project Data Manager Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity,
Astellas is a global life sciences company committed to turning innovative science into VALUE for patients. We provide transformative therapies in disease areas that include oncology, ophthalmology, urology, immunology and womens health. Through our research and
The Senior CRA will provide operational and administrative support to global clinical trial teams involved in New Chemical Entity (NCE) development programs. The role involves coordination of clinical trial documentation, regulatory submissions, site and vendor communications,
The Senior Document Management Associate (SDMA) will provide support for Trial Master File (TMF) activities to the clinical teams for all assigned projects. This role will be responsible for working with study teams, both internal and external,
Job Title: Global Clinical Supply Chain Business Unit: Global External Manufacturing and Supply Chain - Biologics Job Grade Location : Mumbai At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an
Principal Safety & PV Specialist (Literature CP & Review) Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and
Clinical Trial Manager - SCP Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them
Safety & PV Specialist I - Literature Case processing Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and
Summary of Responsibilities: Follow all applicable departmental Standard Operating Procedures and Work Instructions. Complete day-to-day tasks ensuring quality and productivity. Execute high quality, timely monitoring and reporting plan(s) including specialized monitoring requests for approved protocols. Track
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Clinical Trial Coordinator – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750