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Senior Clinical Research Associate jobs at Msd in Malaysia
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11 jobs found
30.06.2024
MSD
MSD Senior Clinical Research Associate Malaysia, Selangor
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Develops strong site relationships and ensures continuity of site relationships through all phases of the trial. Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws...
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30.06.2024
MSD
MSD Clinical Research Associate Malaysia, Selangor
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Based in Malaysia, named one of the Best Companies to Work for in 2019 by HR Asia. We were awarded ‘Sponsor of the Year’ in 2019, 2020 and 2022 from...
28.06.2024
MSD
MSD Clinical Trial Coordinator CTC Malaysia, Selangor
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Based in Malaysia, named one of the Best Companies to Work for in 2019 by HR Asia. We were awarded ‘Sponsor of the Year’ in 2019, 2020 and 2022 from...
30.06.2024
MSD
MSD Country Clinical Quality Manager South East Asia Malaysia, Selangor
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Opportunity to join a leading global biopharma company. Exciting chance to work with passionate and collaborative teams. Be at the centre of innovation and excellence in execution....
Yesterday
MSD
MSD STS Tier Support Associate Specialist Malaysia, Selangor
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Part of a team of STS professionals executing STS SRD Tier2 processes Globally applying “Follow the Sun Model’’. Ensure tickets are taken care with utmost quality and in timely manner...
06.07.2024
MSD
MSD STS Tier Support Associate Specialist Japanese Speaker Malaysia, Selangor
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Part of a team of STS professionals executing STS SRD Tier2 processes Globally applying “Follow the Sun Model’’. Ensure tickets are taken care with utmost quality and in timely manner...
Yesterday
MSD
MSD STS Vendor Master Data Management Initial Reviewer Associate... Malaysia, Selangor
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Position OverviewThe Vendor Master Data Initial Review Associate Specialist is accountable for overseeing the qualification, data analysis, data accuracy, and change control of Master Data. Working independently, this role demonstrates...
Description:Full job details
Develops strong site relationships and ensures continuity of site relationships through all phases of the trial. Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws...
These jobs might be a good fit
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