- GE HealthCare (IL)
- **Job Description Summary** The Pharmacovigilance Agreement Associate , working on the Global Pharmacovigilance Team, will be responsible for supporting ... the preparation and maintenance of GE HealthCare Pharmacovigilance Agreements (PVAs), Safety Data Exchange Agreements (SDEAs), and other related contractual … more
- Organon & Co. (Plymouth Meeting, PA)
- **Job Description** **Position Overview** The Associate Director is responsible for ensuring that Primary Market Research, Competitive Intelligence, and Data ... regulations, Company policies and procedures, and governing body rules and standards. The Associate Director will: + Be a champion for ethical and compliant Primary… more
- Merck (Rahway, NJ)
- **Job Description** ** Associate Director, Regulatory Submissions Archive Operations** Location: Rahway, NJ (Hybrid role - onsite 3 days per week required) Functional ... (RIIM) within Global Regulatory Affairs & Clinical Safety (GRACS) The Associate Director of Regulatory Submissions Archive Operations serves as the Business… more
- Parexel (Columbia, SC)
- …we are expanding our esteemed Medical Sciences Team and seeking an Associate /Medical Director to support the growth of our Global Immunology and Inflammation ... Therapeutic Franchise. As an Associate / Medical Director, you will work closely with...for successful delivery of the projects according to contracted agreement with the sponsor (ie: tasks and time per… more
- Otsuka America Pharmaceutical Inc. (Baton Rouge, LA)
- The Associate Director of Regulatory Intelligence leads the collection and dissemination of regulatory intelligence and collaborates with SMEs to interpret the ... EMA, PMDA, ICH, etc. + General knowledge of global regulations for pharmacovigilance reporting for approved and investigational products. + Confirm list of upcoming… more
- Organon & Co. (Plymouth Meeting, PA)
- **Job Description** **The Position** We are looking for an experienced Associate Director, Program Manager to join our team. This successful candidate will provide ... in R&D functions (eg, Clinical Research, Early Development, Medical Affairs, Pharmacovigilance , Regulatory Affairs, etc.) + At least three years of experience… more
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