Are you passionate about making a difference in the pharmaceutical industry? Do you thrive in a dynamic and innovative environment? If so, you’re in the right place! ProPharma Group is seeking a talented Senior Pharmacovigilance Scientist to join our team in Hyderabad. In this role, you’ll have the opportunity to contribute to groundbreaking research and development initiatives that positively impact patient health and well-being.

About ProPharma Group

ProPharma Group has been at the forefront of advancing scientific breakthroughs for over two decades. As the world’s largest Research Consulting Organization (RCO), we partner with biotech, medical device, and pharmaceutical organizations of all sizes to provide expert advice and innovative solutions across the entire product lifecycle. Our deep domain expertise in regulatory sciences, clinical research, quality & compliance, pharmacovigilance, and medical information enables us to de-risk and accelerate our partners’ most high-profile drug and device programs.

Available Vacancies at ProPharma Group

At ProPharma Group, we are committed to fostering a diverse and inclusive workplace where every individual can thrive. Currently, we have an exciting opportunity for a Senior Pharmacovigilance Scientist to join our team in Hyderabad. This position offers a competitive salary, comprehensive benefits package, and the chance to work alongside industry-leading experts in a collaborative and supportive environment.

Position Title: Senior Pharmacovigilance Scientist

Company Name: ProPharma Group

Salary: Competitive

Job Description of Senior Pharmacovigilance Scientist

As a Senior Pharmacovigilance Scientist at ProPharma Group, you will play a pivotal role in ensuring the safety and efficacy of pharmaceutical products. Your responsibilities will include:

Responsibilities of Senior Pharmacovigilance Scientist

Authoring and reviewing Aggregate reports (PSURs/PBRERs, PADERs/Annual Reports/ ACO/ DSUR) for submission to local and other Health Authorities.
Authoring and reviewing Risk Management Plans (RMPs) as part of regular Pharmacovigilance activities.
Subject matter expert (SME) responsibilities, including training and mentoring of individuals.
Performing literature searches and validity checks for aggregate reports.
Generation of Line Listings (LL) from the safety database.
Providing reliable support for high-priority Ad-hoc activities.
Interacting with appropriate client personnel to resolve issues related to Aggregate reports.

Essential Functions and Necessary Skills

To excel in this role, you must possess the following:

Proficient computer knowledge and keyboarding skills.
Strong verbal, written, and interpersonal communication skills.
Strong organization and prioritization skills.
Flexibility to adapt and meet fluctuating business priorities.
Educational Requirements: PhD, M-Pharmacy/B-Pharmacy, Doctor of Pharmacy (PharmD) from PCI recognized University/College.
Experience Requirements: 2-5 years of experience in authoring ARs and at least 1-2 years of exposure to Quality review.

Company Culture and Commitment to Diversity

At ProPharma Group, we celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion, and we encourage employees to unleash their innovative, collaborative, and entrepreneurial spirits.

Propharma Hiring Senior Pharmacovigilance Scientist Hyderabad