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Clinical Research Associate jobs at Msd in Turkey
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6 jobs found
20.07.2024
MSD
MSD Clinical Research Associate Turkey
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Performs clinical study sitemanagement/monitoringactivities in compliance with Good Clinical Practice and associated documents & regulations,. Collects, reviews, and monitors required regulatory documentation for study start-up, study maintenance and study close-out,....
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14.07.2024
MSD
MSD Clinical Research Associate Manager Turkey
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Work allocation, staff development and performance appraisal. Provides input for capacity planning, including reporting of current manpower and forecasting of - CRA capacity and needs, to provide efficient use of...
20.07.2024
MSD
MSD Senior Clinical Research Associate Turkey
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Performs clinical studysite management/monitoring activitiesin compliance with Good Clinical Practice and associated documents & regulations,. Collects, reviews, and monitors required regulatory documentation for study start-up, study maintenance and study close-out,....
21.07.2024
MSD
MSD Clinical Research Intern Turkey
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Drug & Non-Drug Supply Management. Payment and Invoice Management. Document & report checks from Veeva. Preparation of submissions to regulatory authorities. Management of safety documents. Pre and Post Monitoring Visit...
04.08.2024
MSD
MSD Clinical Research Manager Turkey
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Accountable for performance and compliance for assigned protocols in a country in compliance with ICH/GCP and country regulations, our company’s policies and procedures, quality standards and adverse event reporting requirements...
10.08.2024
MSD
MSD Clinical Operations Manager Turkey
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Ownership of country and site budgets. Development, negotiation and completion of Clinical Trial Research Agreements (CTRA). Provide support and oversight to local vendors as applicable. Interacts with EC and Regulatory...
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Description:Full job details
Performs clinical study sitemanagement/monitoringactivities in compliance with Good Clinical Practice and associated documents & regulations,. Collects, reviews, and monitors required regulatory documentation for study start-up, study maintenance and study close-out,....
These jobs might be a good fit
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