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…?patient journey? and the strategic plan for the compound), medical support for regulatory affairs and interactions with government agencies (medical support for
…functions including Research and Development (RD), Risk Management, Quality/Post-Market Vigilance, Regulatory Affairs , Clinical Research and Medical Affairs ,
J&J Family of Companies
…relationships with the global franchise and regionalcross-funcational partners (Medical Affairs , Clinical Research, Regulatory , HealthEconomics, Marketing, R&D).
Greenville Health System
…and related documents of the clinical research unit are submitted for regulatory review in accordance with Federal Regulations and GHS Policies and Procedures.
Technical Resources International
…writing, IRB activities, infectious diseases, working with HIV patients, and/or regulatory affairs is highly desirable. Technical Resources International is
AstraZeneca Pharmaceuticals LP
…conjugates, underpinned by personalized healthcare and biomarker technologies. Global Medical Affairs (GMA) ensures the best patient outcomes by providing healthcare
…healthcare and biomarker technologies. A Medical Director/Sr Medical Director in US Medical Affairs is a board-certified physician or PhD who has a history of
A Medical Director/Sr Medical Director in US Medical Affairs is a board-certified physician or PhD who has a history of clinical practice or significant industry
…and evaluation of research protocols and procedures with regards to regulatory concerns. Identify research projects that would benefit from consultation. Develop
…adoption * Driving clinical development plans in collaboration with key stakeholders including regulatory affairs , medical affairs and the business. *