- Merck & Co. (Rahway, NJ)
- Job DescriptionOur Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical trials and ... produce safe, effective, innovative medicine.The Global Clinical Data Standards Vocabulary Specialist , Associate Director, is a subject matter expert in CDISC… 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
- Merck (Austin, TX)
- **Job Description** Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical ... safe, effective, innovative medicine. The Global Clinical Data Standards Vocabulary Specialist , Associate Director, is a subject matter expert in CDISC Controlled… more
- Amgen (Washington, DC)
- …best work alongside other innovative, driven professionals in this meaningful role. ** Specialist Technical Business Analyst** **Live** **What you will do** Let's do ... limited to: Java or Python + Proficient with implementation and supporting COTS Pharmacovigilance Platforms (for example Argus) is a plus or other safety database +… more
- ThermoFisher Scientific (Cambridge, MA)
- …on - now and in the future. Location/Division Specific Information Remote/ Pharmacovigilance \#CorEvitas Discover Impactful Work: Quality and accuracy of reporting ... Drug Safety events is a critical function within CorEvitas, part of Thermo Fisher Scientific. This role will support the collection, tracking, data management, adjudication and reporting of adverse events reported by registry sites to support post… more
- Randstad US (Trenton, NJ)
- …occupations + reference47911 job details job summary: The GRADS Compliance Specialist contractor is responsible for executing Regulatory and PV compliance activities ... and management of continuous improvements across the Regulatory and Pharmacovigilance system, including the implementation, tracking, maintenance, and effectiveness… more
- Randstad US (Cambridge, MA)
- …the guidance of the CRD he/she collaborates with the Coding specialist , Biostatisticians, Data Managers, Global and Regional Study Managers, Feasibility Managers, ... Pharmacovigilance representative, Medical Writer (eg planning and review of...cases with the Clinical Trial Team (Monitoring Teams) or Pharmacovigilance . + To better serve the activity, and depending… more
- Lilly (Indianapolis, IN)
- …COE, Discovery and Clinical Research, Business Units).Demonstrate knowledge in pharmacovigilance and risk minimization, which includes and understanding of relevant ... Understanding the roles and responsibilities of the European Union Qualified Person for Pharmacovigilance (QPPV). + Ensure support is provided to enable the QPPV to… more
- Lilly (Indianapolis, IN)
- …level degrees: PhD, PharmD, Nursing with advanced clinical specialty (Clinical Nurse Specialist /Nurse Practitioner). + Combined with a minimum of 1 year experience ... areas relevant to drug discovery or development, eg epidemiology, toxicology, pharmacovigilance , regulatory affairs + Experience within Global Patient Safety or… more
- Bristol Myers Squibb (Chicago, IL)
- …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
- 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 (Washington, DC)
- …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
- AbbVie (Mettawa, IL)
- …Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description Provides specialist medical/scientific strategic and operational input into core medical affairs ... in a relevant therapeutic specialty. Must have an understanding of Pharmacovigilance practices for Clinical Development programs. *Ability to interact externally and… more
- Bristol Myers Squibb (Chicago, IL)
- …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
- Boehringer Ingelheim (Ridgefield, CT)
- …The Associate Director, Medical Coding, Analytics & Process is responsible for specialist expertise in medical coding (MedDRA and WHO Drug Global) both for ... conventions and related trainings. + Firm knowledge of regulatory environment in Pharmacovigilance and GCP. + Experience with clinical trial databases and/or PV… more
- AbbVie (Mettawa, IL)
- …Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description Provides specialist medical/scientific strategic and operational leadership into global oncology ... strategy and the protocols. + Must have an understanding of the Pharmacovigilance practices for Clinical Development programs. + Ability to interact externally and… more
- Organon & Co. (Plymouth Meeting, PA)
- …feasible to execute, efficient and in line with Good Clinical and Good Pharmacovigilance Practice (GCP and GPvP). + Ensure excellent understanding of the external ... sciences activities at Organon. **Required Education, Experience and Skills** + MD specialist , several years of clinical experience exercising medical judgment as a… more
