- Integrated Resources, Inc (Cambridge, MA)
- Job Title: Senior Drug Safety Specialist Location: Cambridge, MA Duration: 8+ Months Job Description: Duties: . Reporting to the Associate Director, Drug ... Safety and Pharmacovigilance Compliance and Operations, you will play a pivotal role in drug safety activities, supporting records management and compliance… more
- 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 ... surveillance, we ensure the safety and efficacy of our existing and pipeline products...safe, effective, innovative medicine.The Global Clinical Data Standards Vocabulary Specialist , Associate Director, is a subject matter expert in… more
- ThermoFisher Scientific (Cambridge, MA)
- …safe and effective treatments to market. Your objectivity and dedication to patient safety will improve health outcomes that people and communities depend on - now ... and in the future. Location/Division Specific Information Remote/ Pharmacovigilance \#CorEvitas Discover Impactful Work: Quality and accuracy of reporting Drug … more
- Grifols Shared Services North America, Inc (Los Angeles, CA)
- …and guidelines + Expertise in therapeutic products and areas; medical coding; safety -data administration + Pharmacovigilance Specialist should possess ... 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 ... チーム全体で以下の業務を担っています。中心業務の他については、これまでのご経験に合わせて分担して対応いただきます。 GVPに基づく安全性情報の処理 + 入手した安全管理情報の処理（評価・安全性データベースへの入力・評価資料の作成・フォローアップ等）: 使用する安全性データベースはGlobal safety databaseであり、入力言語は英語 + 安全性評価／安全対策に係る案件に関する当社Global Head… more
- University of Southern California (San Diego, CA)
- …investigator, internal and external project team meetings. + Assists in overseeing the Medical Safety Specialist team within the Medical Safety unit + ... questions, assists in evaluating AEs and SAEs, laboratory and other safety parameters, medical history, and concomitant medications. + Assesses and evaluates… more
- Merck (Austin, TX)
- **Job Description** Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical ... trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products...effective, innovative medicine. The Global Clinical Data Standards Vocabulary Specialist , Associate Director, is a subject matter expert in… 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 ... or Python + Proficient with implementation and supporting COTS Pharmacovigilance Platforms (for example Argus) is a plus or...Platforms (for example Argus) is a plus or other safety database + Knowledgeable of Agile project methodologies and… 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
- Lilly (Indianapolis, IN)
- … pharmacovigilance , regulatory affairs + Experience within Global Patient Safety or demonstrated knowledge and understanding of pharmacovigilance , ... through philanthropy and volunteerism. **Purpose:** The purpose of the Medical Device Safety Scientist Associate Director role is to leverage clinical and scientific… more
- Randstad US (Cambridge, MA)
- …data validation and review processes, support the CRD for the Clinical Case review ( safety events reported to Pharmacovigilance or safety events of special ... neuroscience + Medical writing experience (drafting consents or protocols) + Medical safety experience is a plus skills: Pharmacovigilance , Data Validation Plan,… more
- Lilly (Indianapolis, IN)
- …of the Clinical Research Scientist, GPS Medical is to perform clinical safety functions within Global Patient Safety Medical, including supporting ... safety expertise. The CRS will support the management and evaluation of safety information by performing medical monitoring of individual case reports (ICRs) and… 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 ... execution of clinical trial support activities (as per established scope documents) ** Pharmacovigilance ** + Ensures that FM team has the required knowledge to… more
- AbbVie (Mettawa, IL)
- …Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description Provides specialist medical/scientific strategic and operational input into core medical affairs ... (medical education, data, guidelines and value proposition); safeguarding patient safety (risk minimization activities / safety surveillance activities).… 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 ... processes to secure an industry-benchmarked clinical development and clinical safety organization, operating in full compliance. + Ensure proactive intelligence… 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 ... clinical study databases and the global safety database, including the conception, planning and execution of...related trainings. + Firm knowledge of regulatory environment in Pharmacovigilance and GCP. + Experience with clinical trial databases… more
- Bristol Myers Squibb (Los Angeles, CA)
- …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
