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responsibilities: set up, maintain and review trial master files including supporting Quality Control of documents support the clinical team in all aspects of the organization and management of Clinical trials according to ich-gcp, applicable .....
job description join us on our exciting journey! iqvia™ is the human Data Science company™, focused on using data and science to help Healthcare clients find better solutions for their patients. formed through the merger of ims Health and .....
job description join us on our exciting journey!iqvia™ is the human Data Science company™, focused on using data and science to help Healthcare clients find better solutions for their patients. formed through the merger of ims Health and .....
job description q2 solutions comprises quintiles’ former global central laboratories, bioanalytical/adme and Genomics businesses and quest Diagnostics’ former Clinical trials business.descriptionwe are always looking for new talent to join q2 .....
this position reports into the office of the pst (part of the Strategy management office) in the Pharmacovigilance and Patient Safety (pps) organization. the pps organization works collaboratively and strategically with colleagues across the product .....
job description q2 solutions comprises quintiles’ former global central laboratories, bioanalytical/adme and Genomics businesses and quest Diagnostics’ former Clinical trials business.descriptionwe are always looking for new talent to join q2 .....
job description q2 solutions comprises quintiles’ former global central laboratories, bioanalytical/adme and Genomics businesses and quest Diagnostics’ former Clinical trials business.descriptionwe are always looking for new talent to join q2 .....
 we believe that our people are the future of the industry. we provide a culture in which our employees can enjoy personal satisfaction, professional achievement and have the ability to strategically map out long-term Career plans. if you're .....
purpose/objective of the job·        conduct Good Clinical Practice (gcp) and Pharmacovigilance (pv) audits as above described.·        act as project-specific liaison between r&d quality - ct&s and key stakeholders, .....
    position summary the Medical Director, Risk Management Pharmacovigilance is accountable for executing the safety and Risk Management activities for one or more assigned Clinical Development projects or marketed products to enable the safe and .....
865 jobs

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