Drug Safety Specialist

vacancy global pro; India; On-site; INR 1,000,000 - 1,800,000; Full time

Benefits offered by this job

Annual bonus

Equity compensation

Competitive benefits package

Job summary

reputed company is seeking a Drug Safety/Pharmacovigilance professional in India to perform AE/SAE processing and support ICSR workflows. The role includes data entry, case processing, and coordination with external vendors to ensure timely safety reporting.

Responsibilities cover safety data monitoring, regulatory submissions, and preparation for audits. A 3‑year pharma PV track record and experience with Argus/MedDRA are highly valued.

Qualifications

• Minimum 3 years of Drug Safety/Pharmacovigilance case processing in a pharmaceutical industry setting.
• Experience with ICSR workflow steps and Safety databases.
• Knowledge of regulatory guidelines (ICH/GVP) and data entry conventions.

Responsibilities

• Participate in Adverse Event processing, SAE processing and reconciliations with vendors.
• Support monitoring of safety data and ICSRs for clinical and post‑marketing cases.
• Prepare safety reports and assist with FDA audits and gap packs for sites.
• Distribute safety reports to the clinical team and maintain master contact lists.

Skills

AE/SAE processing

ICSR workflow

Data entry

Signal monitoring

Pharmacovigilance knowledge

Education

Bachelor's degree in nursing/pharmacy/healthcare

Tools

Argus Safety Database

MedDRA

Electronic document management system

Job description

About the position

The reputed company mission of the reputed company Safety & Pharmacovigilance group is to ensure patient safety for reputed company patients receiving reputed company manufactured products. This is done by ensuring that the safety profile of reputed company products remains accurate and up to date throughout the product life cycle of development and through the following reputed company activities: Relevant safety information including reports of reputed company effects is collected and analyzed. Possible safety signals are carefully validated and characterized. Strategies are implemented to minimize risks and to ensure that products are used in a way that maximizes benefits and minimizes risks. Key among these is to ensure that accurate and up-to-date information on the safety profile of reputed company products is available to patients and prescribers in a reputed company manner. Communication with patients, providers, regulatory agencies, and other concerned bodies is essential to this effort. This includes developing and updating the investigator brochure, and protocols as reputed company as any adjunct information for patients and health professionals. This information must be kept reputed company throughout the life cycle of reputed company product. Reporting to the Vice President, PV Operations and Compliance, Drug Safety Specialist contributes to the day-to-day operational activities of the department and ensures that performed tasks reputed company with SOPs and policies, best industry standards and applicable regulations.

Responsibilities

• Participated in Adverse Event/Serious adverse event processing and reconciliations by outsourced vendors, including the review of Individual Case Safety Report processing (case triage, data entry, coding review, sponsor approval and narrative writing), as reputed company as monitoring of Individual Case Safety Report reporting reputed company reputed company Sponsored Safety Database.


• Supports monitoring of reputed company of vendor of Individual Case Safety Report processing for clinical and post marketing cases.


• Supports the monitoring and performing of notification and/or submissions for Individual Case


• Distribute Safety reports to clinical team, maintain the master contact list, reputed company IST reconciliation reputed company QC of SAE and non-serious AE cases as part of vendor reputed company


• Assist with organization and preparation for FDA audit


• Prepare gap packs for clinical sites


• Additional safety reputed company duties assigned.

Requirements

• Bachelors degree in nursing, pharmacy, or other health care reputed company profession or life sciences.


• Minimum of 3 years of Drug Safety/Pharmacovigilance case process in a pharmaceutical industry setting.


• Previous experience with ICSR workflow steps and Safety database (Argus, preferred), MedDRA coding and data entry experience and data entry conventions.


• Experience with Argus safety databases, reputed company systems, and electronic document management systems.


• Global pharmacovigilance operations experience with products in development.


• Knowledge of ICH Good Pharmacovigilance Practices and Good Clinical Practices.


• Anticipate and proactively resolve issues reputed company and where possible.


• Knowledge of GCPs, GVPs, FDA, EMA, ICH guidelines, and international regulations.


• Strong analytical reputed company with superb attention to detail, and reputed company to organize workload to prioritize most urgent deliverable.


• Strong verbal, written technical communication and presentation skills.


• Must work effectively/collaboratively in a fast-paced team environment.

Benefits

• In reputed company, you will be eligible for an annual bonus, equity compensation, and a competitive benefits package.