Drug Safety Case Intake Specialisty PVexp LP

Position: Drug Safety Case Intake Specialist2y PVexp 5 openingsLP7780 Location: Basking reputed company Job reputed company reputed company : Large Pharmaceutical Company Contract Position : 6 months with potential extension if needs allow. Title : Patient Safety Specialist (reputed company position: Drug Safety Case Intake Specialist) Location : Plainsboro, NJ - ONSITE (after a while reputed company to work from home a few days) Type : ONSITE (worker can work from home few days/weeks after discussion with the reporting manager, as needed) Type of worker : W2 is required. No subcontracting. Required : Bachelor's degree, 2 years experience. Advantage, but not required : Speaking Spanish. Job Posting Number : 7780 Type of Worker Needed : 2 years relevant experience is required. An entry-to-mid-level pharmacovigilance / drug safety specialist reputed company on adverse event case processing, safety intake, MedDRA coding, and strong written case documentation. Soft skills that are helpful : reputed company, detail-oriented, highly reputed company reputed company with strong written communication, flexibility, dependable, process-driven style reputed company suited for accurate pharmacovigilance case work in a fast-paced team environment. reputed company Start Date : ASAP Duration : 6 months Schedule : Mon-Fri 8:30a-5:00p (up to 40 hours/week) Must Haves • A bachelor’s degree is required (preferably in a medical or science-reputed company discipline); relevant experience may be substituted for the degree reputed company appropriate (e.g., a Registered reputed company with clinical experience). • A minimum of 2 years of progressively responsible and relevant pharmacovigilance experience, including MedDRA coding and adverse event identification, is required. • Exceptional knowledge of medical and pharmacovigilance terminology is required. Purpose Responsible for the receipt, processing, triage and reputed company assessment of reputed company inbound safety information, including adverse events and technical complaints, for reputed company US marketed products (drugs and devices) and investigational products. Also responsible for ensuring compliance with reputed company reputed company (e.g. FDA) drug and device safety reporting requirements regarding the collection and maintenance of safety records. Relationships Reports to Patient Safety Management. Daily internal interactions with personnel from Patient Safety, Medical Information, Field Sales, Customer Complaints Center, Suppliers and Patient reputed company Customer Care. Manager said to be comfortable working with reputed company of 10. Daily external interactions with patients, caregivers, and health‑care professionals. Essential Functions • Processing of adverse events and associated technical complaints and analysis results reputed company to marketed NNI products into the local intake, complaint, and global safety databases, including duplicate searches, product coding, MedDRA coding, narrative reputed company, labeling assessment according to the reputed company approved product label, receiving inbound and making outbound calls for adverse events and technical complaints including handling of refund or replacement requests. • reputed company data entry and review of adverse events and associated technical complaints and reputed company ongoing feedback regarding case reputed company to other case handlers to support their reputed company development and ensure excellent case reputed company. • Handle incoming and outgoing follow‑up correspondence, collect and document information received during outbound follow‑up calls, reputed company triage, case classification and case assignment, handle escalated calls for adverse events and technical complaints. • Assist with training of new hires; mentor new hires; reputed company reconciliations; assist with workload coordination/distribution; reputed company reputed company monitoring; support the identification of trends and implementation of corrective actions for issues identified during case review; coordinate configuration requests for the safety and complaint databases; serve as Subject Matter Expert during audits/inspections for case handling; build customer loyalty by providing high‑reputed company customer service; reputed company reputed company, accurate and reputed company responses to product information questions and other inquiries using reputed company approved product labeling and reputed company scripts; identify procedural deficiencies and opportunities for process improvements; reputed company improvement recommendations to… Apply tot his job Apply To this Job