- United Therapeutics (Concord, NH)
- …and compliance with respect to ISCR processing and reporting. The Lead Pharmacovigilance QC Specialist provides strategic oversight of end-to-end case safety ... biology, or BSN, and 8+ years of experience in pharmacovigilance in either case processing or quality assurance of...chemistry or biology, and 6+ years of experience in pharmacovigilance in either case processing or quality assurance of… more
- Merck (Rahway, NJ)
- **Job Description** **The Senior Specialist , Global Pharmacovigilance will be responsible for some or all of the following core activities:** + Case ... external stakeholders (eg, Competent Authorities) for products for which the Senior Specialist is responsible + PV Statement preparation in compliance with relevant… 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 ... Rhythm's safety vendor. This position will report to the Director of Pharmacovigilance . Responsibilities and Duties + Reviews adverse event information received for… more
- US Tech Solutions (CA)
- …* Perform **quality review** of **external providers'** reconciliation tasks for clinical and post-marketing ( **medical information, product complaints, and ... This role will be 100 % remote. Candidates must posses **3 to 5 years of experience** or application/environment specific knowledge to perform tasks where large quantities of information, data or documents need to be maintained or manipulated in a **structured… more
- Cardinal Health (Indianapolis, IN)
- Job Description **Senior Consultant, Product Sales Specialist - NPHS** **The territory covers Indiana, Michigan, Ohio, Kentucky, Missouri** The Product Sales ... Specialist is responsible for developing opportunities, selling, growing and...stakeholders. + Be very familiar with and observe all pharmacovigilance policies and procedures and ensure that any product… more
- Merck (North Wales, PA)
- **Job Description** **Position Overview:** This Senior Specialist position is part of the GRACS US Subsidiary function within our Research & Development Division. ... the direction of the Senior Director and Associate Director, the Senior Specialist Financial Disclosure US Subsidiary role is responsible for the tracking,… more
- AssistRx (Kansas City, MO)
- The Vendor Management Specialist at AssistRx is responsible for managing the full lifecycle of vendor relationships to ensure alignment with organizational policies, ... the Compliance Department, including audits, hotline management, internal controls, pharmacovigilance , document control, training, risk management, business continuity, CAPA… more
- Grifols Shared Services North America, Inc (Research Triangle Park, NC)
- …every clinical study + **Qualification and periodic assessment of clinical and pharmacovigilance vendors participating in the clinical studies** + Perform a quality ... assessment (including a risk assessment) of all the vendors selected as candidates to participate in the clinical studies + Qualify the clinical vendors before their participation in the clinical studies and re-qualify them when applicable + Perform an annual… more
- AbbVie (North Chicago, IL)
- …is a robust, two-year rotational program specifically targeting Medical Doctor (MD) specialist talent (graduating fellows). Those who have completed their MD program ... considered. The goal of the program is to develop and support high-potential specialist physician talent in transitioning to a successful career within R&D at… more
- AbbVie (North Chicago, IL)
- …is a robust, two-year rotational program specifically targeting Medical Doctor (MD) specialist talent (graduating fellows). Those who have completed their MD program ... considered. The goal of the program is to develop and support high-potential specialist physician talent in transitioning to a successful career within R&D at… more
- Bristol Myers Squibb (Philadelphia, PA)
- …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