Clinical Research Regulatory Specialist
We have 91 ads for keyword clinical research regulatory specialist
(0.001 seconds)Study Startup Lead
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Full-time Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A
Associate Study Start-Up Manager | REE419
Job Overview Direct and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol
(K295) Literature science Specialist
Why join Stryker? We are proud to be named one the World's Best Workplaces and a Best Workplace for Diversity by Fortune Magazine! Learn more about our
Statistical Programming Associate Director
Do you have expertise in and passion for statistical programming and understanding of drug development programs? Would you like to apply your skills to
Associate Director Statistical Programming
Do you have expertise in and passion for statistical programming and understanding of drug development programs? Would you like to apply your skills to
Study Startup Lead
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Full-time Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A
Regulatory Affairs Specialist
Department: Global Regulatory Affairs Are you passionate about what you are doing? Do you want to build excellence within processes in the most efficient way?
Senior Software - Java full stack and cloud
JOB TITLE: SENIOR CONSULTANTCAREER LEVEL: D1 Leverage technology to impact patients and ultimately save lives Do you have expertise in, and passion for,
Study Startup Lead
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Full-time Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A
Site Identification Specialist (Feasibility)
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Full-time Company DescriptionWe are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A
[OY340] - Senior regulatory writer
900! That is the approximate number of individual regulatory documents the dynamic team at Regulatory Writing and Submissions (RWS) planned, developed and
Site Identification Specialist (Feasibility)
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Full-time Company DescriptionWe are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A
Senior Quality Assurance Specialist
The Senior Quality Assurance Specialist works in a Good Clinical Practices compliant setting as part of a global team, assessing quality compliance,
Study Start:Up Specialist (SSUS)
Job Location: Bangalore Are you experienced Clinical research professional and passionate about clinical trials? Does being part of a growing, yet dynamic
Technical Service : Specialist 1
For 70 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join
Study Startup Lead
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Full-time Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A
[MF-939] | Assoc Centralized Monitoring Lead
JOB DESCRIPTIONJob OverviewProvides support to CMS leads on activities related to the CMS team, in partnership with project and clinical lead, and in
Technical Service : Specialist 1
For 70 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join
ZUO93 Reg Intelligence Specialist
Job description Essential Function - Acts as a Regulatory Team Leader on more complex projects, which may include technical writing; - Prepares and / or
Senior Quality Assurance Specialist
The Senior Quality Assurance Specialist works in a Good Clinical Practices compliant setting as part of a global team, assessing quality compliance,