At Merck, known as MSD outside of the United States and Canada, we are unified around our purpose: We use the power of leading-edge science to save and improve lives around the world. For more than 130 years, we have brought hope to humanity through the development of important medicines and vaccines. We aspire to be the premier research-intensive biopharmaceutical company in the world – and today, we are at the forefront of research to deliver innovative health solutions…
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Full company description
At Merck, known as MSD outside of the United States and Canada, we are unified around our purpose: We use the power of leading-edge science to save and improve lives around the world. For more than 130 years, we have brought hope to humanity through the development of important medicines and vaccines. We aspire to be the premier research-intensive biopharmaceutical company in the world – and today, we are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. We foster a diverse and inclusive global workforce and operate responsibly every day to enable a safe, sustainable and healthy future for all people and communities. For more information, visit www.merck.com.
This site is intended for residents of the United States and Canada and their territories only. FLS: http://merck.us/3TKXNuZ
LinkedIn followers
2,737,187
People associated on LinkedIn
44,477
Reported office locations
126 E Lincoln Ave, P.O. Box 2000, Rahway, New Jersey 07065, US
351 N Sumneytown Pike, North Wales, PA 19454, US
Other recorded names
Merck, S.A. - Panama
Merck Regional Headquarters LLC
Merck S.A.
Merck LLC
Merck C.A.
Merck Ilac
Merck
Specialties
Pharmaceutical
Profile identifies a recruitment agency
No
Industry
Pharmaceutical Manufacturing
Size
10,001+ employees
Headquarters
Rahway, New Jersey
Organization type
Public Company
Specialties
Pharmaceutical
Merck Sharp & Dohme LLC has 1 open jobs in Canada as of November 6, 2026.
4+ YOEExpertise in clinical data standards development and implementation; Deep knowledge of CDISC CDASH, SDTM and Controlled Terminology; Experience in clinical trial data management and regulatory requirements