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1747 jobs

bristol-myers squibb is a global biopharmaceutical company focused on discovering, developing and delivering innovative medicines for patients with serious diseases. our medicines are helping millions of patients around the world in disease areas .....
descriptionthe product safety specialist is responsible for receipt and Documentation of safety information for marketed and investigational products. interacts with Health professionals and consumers to obtain and follow-up reports of possible .....
teva is a global Pharmaceutical Leader and the world’s largest generic medicines producer, committed to improving Health and increasing access to quality Health solutions worldwide.  our employees are at the core of our success, with .....
    position summary the Associate Director, global ds operations lead is responsible for ensuring the proper execution and implementation of drug safty operational activities within global Drug Safety, study management teams, Clinical operations, .....
responsibilities department description:the Health safety and environmental group (hse) is responsible for implementing programs and policies that comply with all local, state and federal hse rules and regulations and continuously strive to reduce .....
solvay is an equal opportunity employer. we evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other legally protected characteristics. .....
job description dupont has a rich history of scientific Discovery that has enabled countless innovations and today, we're looking for more people, in more places, to collaborate with us to make life the best that it can be. as a Member of the global .....
purpose/objective of the jobthe ad of gq ct&s risk assessments is an essential role to lead the enterprise risk assessments related to Clinical trials. this role reports to the head of gq ct&s quality governance and risk assessments.key .....
description\:   the Director has responsibility for the Pharmacovigilance Risk Management activities of core strategic * marketed and/or investigational compounds on global level. in additional to reporting to us Line Management, this position .....
correct title: senior manager, trial safety science core work hours - 8 hour day as long as core hours of 9am-4pm are covered. extension of the contract will be contingent upon performance. work site: summit, nj. general responsibilities: • .....
1747 jobs