- Boehringer Ingelheim (Ridgefield, CT)
- …review of team output. + Provide updates of the assigned drug 's safety profile to senior management and recommend pharmacovigilance / risk management ... **Description** Director OR Senior Associate Director has responsibility for the pharmacovigilance...compounds. + Plan, manage / perform and monitor all pharmacovigilance activities for assigned drug responsibilities, including:… more
- Ascendis Pharma (Princeton, NJ)
- …8 years recent experience in Pharmacovigilance + Working knowledge of validated Drug Safety Databases (Argus preferred) + Experience with MedDRA coding and ... + Reviews and provides input to Business Partner or Pharmacovigilance Agreements and Safety Data Exchange Agreements...health care field with relevant pharmaceutical industry experience in drug safety . + Candidates with advanced scientific… more
- ThermoFisher Scientific (Greenville, NC)
- …(comparable to 1-2 years) in the industry; Or + Direct experience in safety / Pharmacovigilance medical monitoring (comparable to 2 years). + For Medical Director ... (comparable to 2+ years) in the industry; Or + Direct experience in safety / Pharmacovigilance (comparable to 2+ years) + Preferences are towards individuals with… more
- Astellas Pharma (Northbrook, IL)
- …teams. 1. ** Pharmacovigilance (6 months)** + Develop hands-on experience in safety monitoring and risk management throughout the drug lifecycle. + Develop ... diverse rotations-Clinical Development (12 months), Medical Affairs (6 months), and Pharmacovigilance (6 months), Participants will gain hands-on exposure to key… more
- ThermoFisher Scientific (Greenville, NC)
- …background check, which includes a drug screening. Our detailed, goal-oriented Pharmacovigilance colleagues manage the safety profile of new drugs in ... experience working on clinical trials through every stage of drug development. This includes management and oversight of all...years) in the industry; Or + Direct experience in safety / Pharmacovigilance (comparable to 2 years) **For Medical… more
- System One (East Windsor, NJ)
- Job Title: Quality Compliance Associate Location: East Windsor, New Jersey Type: Contract Compensation: $26 - $36 per hour Contractor Work Model: Onsite Hours: 8/9 ... Sterile Injectable Products Responsibilities: + Under the oversight of the Associate Manager of Quality Assurance (QA) Compliance, this position will be… more
- Sumitomo Pharma (Annapolis, MD)
- …including authoring clinical sections for INDs, NDAs, and other related documents. + Partner with Drug Safety & Pharmacovigilance to assess the safety ... a dynamic, highly motivated, and experienced individual for the position of ** Associate ** **Medical Director, Clinical Development - Oncology** . The associate … more
- Merck (Rahway, NJ)
- …for interacting with health agencies (eg FDA); understand key elements in pharmacovigilance , drug safety monitoring, signal detection and processing ... of study findings; (b) **Global Regulatory Affairs and Clinical Safety :** Focus on late-stage and lifecycle drug ...Clinical Safety :** Focus on late-stage and lifecycle drug activities, understand key regulatory policies and the procedures… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …inspire you and empower you to shine? Join us as an Associate Medical Director, Clinical Science, Neuroscience- Pulmonologist/Neurologist in our Cambridge, MA ... a vital contributor to our inspiring, bold mission. **POSITION OBJECTIVES:** The Associate Medical Director leads and drives strategy for the overall global… more
- Bristol Myers Squibb (Madison, NJ)
- …(SBRA) Lead will report into the Structured Benefit-Risk Assessment Head within Safety Evidence and Sciences and will be accountable to lead structured benefit-risk ... collaboration with relevant departments across the organization, including medical safety assessment, clinical development, global regulatory, epidemiology and others.… more
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