- Merck & Co. (Rahway, NJ)
- Job DescriptionPosition Description: Senior Specialist , Clinical Literature MonitoringProvides pertinent and timely information on our Company's products and ... search request results meet current regulatory requirements Collaborates with pharmacovigilance teams to meet current literature-related adverse event monitoring… more
- Merck & Co. (North Wales, PA)
- Job DescriptionOur Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new ... data governance reviewsThe Global Clinical Data Standards (GCDS) Data Standards Specialist may contribute to the definition and maintenance of business processes… more
- Merck & Co. (Rahway, NJ)
- …the pharmaceutical industry (eg, Medical Affairs, Regulatory Affairs, Clinical, Pharmacovigilance ).- - Required experience and skills: Project management skills with ... the ability to handle multiple projects and prioritize work accordingly. Tolerance for ambiguity and action oriented. Strong written and oral communication skills. Attention to detail and accuracy. Ability to influence and negotiate. Ability to distill an… more
- Careerbuilder-US (Millsboro, DE)
- Job Title: Biological Labeling Specialist Job Location: Millsboro, DE Job Duration: 14 Months+ Schedule: Hybrid schedule (require to be onsite for 3 days/week ... labels and artworks and liaises with departments such as Marketing, Pharmacovigilance and Technical Services to ensure compliance with established regulations.… more
- Careerbuilder-US (De Soto, KS)
- Job Title: Biologicals Labeling Specialist Job Location: DeSoto, KS Job Duration: 15 months+ Shift: 8 AM - 5 PM Job Description: This position is responsible but is ... labels and artworks and liaises with departments such as Marketing, Pharmacovigilance and Technical Services to ensure compliance with established regulations.… more
- Integrated Resources, Inc (Rahway, NJ)
- Job Title: Labeling Specialist Job Location: Rahway, NJ Job Duration: 12 months+ Shift: Hybrid (3 days onsite) Job Description: * Under general supervision, ... of labels and artworks and liaises with departments such as Marketing, Pharmacovigilance and Technical Services to ensure compliance with established regulations. *… more
- Nesco Resource (Jersey City, NJ)
- …towards a more lean and efficient procedural document framework governing pharmacovigilance and safety surveillance at client. Qualifications: Advanced knowledge of ... end-to-end PV procedural requirements Ability to review/direct PV procedural documents to ensure compliance with international standards and regulations while also promoting a lean and efficient procedural framework. Mid-level understanding of quality… more
- Grifols Shared Services North America, Inc (Los Angeles, CA)
- …in therapeutic products and areas; medical coding; safety-data administration + Pharmacovigilance Specialist should possess autonomy and sense of responsibility, ... and regions. **_Job Summary:_** Provides operational support for global pharmacovigilance activities of Grifols marketed products. Ensures pharmacovigilance … more
- Mallinckrodt Pharmaceuticals (Jobe, MO)
- Job Title 安全管理（ファーマコビジランス）業務従事者/Senior Specialist , Pharmacovigilance Requisition JR000012874 安全管理（ファーマコビジランス）業務従事者/Senior Specialist , Pharmacovigilance ... (Open) Location Kobe - JPN304 Additional Locations Kobe Job Description 医療用医薬品の安全管理業務を中心に担っていたいだくポジションです。担当いただく製品は国内外で販売されており、当該医薬品の個別症例情報・文献情報の取扱いとそれらに関連する業務を中心に担っていただきます。業務にあたってはGlobal PVチーム及び国内提携会社との連携も必要となります。… more
- Rhythm Pharmaceuticals (Boston, MA)
- …learn, and our tenacity to overcome barriers, together. Opportunity Overview As a PV Specialist , you will have a critical role in shaping the pharmacovigilance ... This newly created position will report to the Associate Director of Pharmacovigilance . Responsibilities and Duties + Reviews adverse event information received for… more
- Actalent (St. Louis, MO)
- Remote Pharmacy Technician; specializing in Pharmacovigilance Hiring Pharmacy Technicians to work remotely and ensure drug safety. Will identify and document cases ... of adverse effects of medicines and vaccines. Data input and manipulation using ScriptMed and Microsoft word, Excel, and PDF Will work very closely on a remote team of medical professionals to ensure daily and weekly goals are met. Will complete 33 reports per… more
- Randstad US (Cambridge, MA)
- specialist , global case management. + cambridge , massachusetts (remote) + posted 1 day ago **job details** summary + $40 - $50 per hour + contract + bachelor degree ... poising the company for substantial growth in the upcoming years. The Specialist , Global Case Management will provide critical support to the company's future… more
- Merck (North Wales, PA)
- **Job Description** **Position Description:** Senior Specialist , Clinical Literature Monitoring Provides pertinent and timely information on our Company's products ... request results meet current regulatory requirements + Collaborates with pharmacovigilance teams to meet current literature-related adverse event monitoring… more
- Merck (North Wales, PA)
- **Job Description** Our Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new ... governance reviews + The Global Clinical Data Standards (GCDS) Data Standards Specialist may contribute to the definition and maintenance of business processes… more
- Merck (Rahway, NJ)
- …the pharmaceutical industry (eg, Medical Affairs, Regulatory Affairs, Clinical, Pharmacovigilance ). **Required experience and skills:** + Project management skills ... with the ability to handle multiple projects and prioritize work accordingly. + Tolerance for ambiguity and action oriented. + Strong written and oral communication skills. + Attention to detail and accuracy. + Ability to influence and negotiate. + Ability to… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …directly to the VP, GMS&G. **Responsibilities:** + Co-manage and support Clinical Safety Specialist (CSS) for their respective BU + Responsibility in the area of ... VP, Global Medical Safety and Governance + Oversight for central MA BD Pharmacovigilance + Participation in oversight activities (eg, Clinical Safety and Drug Safety… more
- Boehringer Ingelheim (Ridgefield, CT)
- …candidate will be experienced in clinical research and would be an MD, Retinal Specialist with experience in late stage clinical trials. As an employee of Boehringer ... of cross-functional evidence team (Clinical Operations, Biostatistics, Translational Medicine, Pharmacovigilance , Regulatory, Medical Affairs, Market Access, Epidemiology, RWE etc)… more
- Bristol Myers Squibb (San Antonio, TX)
- …the community, facilitated by their commercial counterpart, TAS (Therapeutic Area Specialist ), to answer unsolicited off-label and technically complex questions in ... agreed upon with home office medical and GDO + Ensure that BMS Pharmacovigilance procedural documents are understood and applied by investigators of local studies,… more
- Bristol Myers Squibb (Philadelphia, PA)
- …of gaps in FM resources; collaborates with the Field Medical Communication Specialist (FMCS), TA point, Medical Information and Medical Strategy on development of ... Adverse Events (AEs) and fully understand and comply with BMS Pharmacovigilance SOPs regarding identification and reporting timelines + Contributes to managing… more
- International Rescue Committee (New York, NY)
- …teams during country program led procurements. * Serve as subject matter specialist to HQ and Country Program Supply Chain staff on pharmaceutical regulations, ... prequalification, quality assurance and control, cold chain storage, distribution, and pharmacovigilance . * Good planning and coordination skills and ability to… more
