Drug Safety Associate at Zydus Pharmaceuticals

Hopewell Township, New Jersey, United States -

Full Time

Start Date

Immediate

Expiry Date

15 Jun, 26

Salary

0.0

Posted On

17 Mar, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Adverse Event Reporting, Pharmacovigilance, FDA Regulations, ICH GCP, GVP Standards, Safety Database, Case Narratives, Seriousness Evaluation, Expectedness Evaluation, MedDRA Coding, ICSR Processing, Product Complaints, Data Reconciliation, Quality Review, Regulatory Inspections, Risk Benefit Analysis

Industry

Pharmaceutical Manufacturing

Description

Description SUMMARY: Responsible for executing US Adverse Event and Pharmacovigilance activities as required by FDA Regulations. Provide support and oversight in drug safety related activities including Product Quality Complaints and Medical Information activities. Zydus Pharmaceuticals (USA) Inc. is a globally integrated generic pharmaceutical company with a focus on providing high service, quality, and affordable products. Our US leadership, which has over 60 years of US generic market experience, understands the customer’s business which allows Zydus the ability to provide unique models to help drive their customer’s success. Our parent company, Zydus Cadila, has a large presence in global markets, including relationships with many top tier international pharmaceutical companies. Based on a manufacturing and development history that spans over 50 years, it is the 4th largest pharmaceutical company in India. RESPONSIBILITIES: · Serve as second line of contact for the incoming calls to medical affairs department. · Intake new and follow up spontaneous Adverse Events and record the discussion in relevant AE worksheet · Writing case narratives for serious/non-serious, study reports and quality/ product complaint reports prior to sign off by medical information manager or Global Pharmacovigilance Team (GPV) · Evaluate cases for seriousness and expectedness criteria. · Enter in AE cases in safety database in timely manner for further processing by MIS and Pharmacovigilance Group. · Maintain Adverse event and safety database log and coordinate distribution of safety data as needed. · Maintain verification of reconciliation and email correspondence in Drug Safety shared drive · Distribute adverse event reports to plant QA/GPV/ partner companies in accordance with Safety Data Exchange Agreements (SDEAs) · Obtain follow-up information via mail or telephone from healthcare professionals and consumers as per the relevant SOP or as per the ongoing medical conditions. · Monitor status of follow-up letters to ensure follow-up information is requested in the required timeframes. · Follow up with reporter/ patient/ HCP at defined interval either by phone or email. · Maintain US Adverse Event and safety database and coordinate distribution of safety data. · Interact with data intake and entry group to ensure complete quality and output and provide guidance on follow up as needed. · Handling Product Complaints related to Adverse Events. · Performing reconciliation with business partners and vendors for AE reports exchanges · Responsible for taking appropriate decisions by applying knowledge of FDA and ICH GCP and GVP standard regulations to write overall case summary. · Assist with Pharmacovigilance reconciliation of databases and listings (post marketing and clinical trial sources) as required. · Perform Quality Review on safety database for other Drug Safety Associate’s cases. · Assist with additional drug safety activities as required. · Perform retrospective equality review and document findings, and contribute to metric compilation · Support the identification of corrections and creation of updates in safety database following medical review. · Implement and execute QC on key fields for serious cases. · Offer during reviews and audits of safety data and database. · Perform Individual Case Safety Report (ICSR) processing activities within the safety database and do quality checks on the assigned ICSR. · Support for Regulatory Inspections. · Ability to distinguish and analyze the ratio of risk and benefits of the drug that is marketed. · Database searches, as necessary. Requirements QUALIFICATIONS – SKILLS & REQUIREMENTS: · Hands on experience with safety database, i.e. ARGUS, ARIS-G, PVNet or other · Extensive working knowledge of FDA regulations, FDA guidance and ICH guidance; some familiarity exposure to EMEA regulations · In-depth understanding of the ICSR assessment and reporting process · Proficient in outlook, MS Word, PowerPoint and Excel. EDUCATION & EXPERIENCE: · Bachelor’s Degree in life sciences, pharmacy, nursing (RN, RPh) or combination of Health-Related Degree and clinical experience in a medical setting. · Two years of experience in pharmaceutical drug safety/pharmacovigilance including experience in triaging of cases, coding of terms using MedDRA, data entry and narrative writing. TRAVEL: · As and when required.

Responsibilities

The associate is responsible for executing US Adverse Event and Pharmacovigilance activities according to FDA regulations, including serving as a second line of contact for medical affairs calls and intake/recording of spontaneous Adverse Events. Key duties involve writing case narratives, evaluating seriousness and expectedness, entering cases into the safety database, and distributing safety data reports.