Are you searching for rewarding Pharma jobs in India? ProductLife Group, a leading name in the pharmaceutical industry, is hiring a Clinical Safety Associate to join their dynamic team. This remote, full-time opportunity, posted on March 03, 2025, is perfect for professionals with a background in pharmacovigilance and drug safety. If you’re passionate about contributing to clinical safety and advancing your career in the pharma sector, this could be your next big step. Read on to explore the job details, responsibilities, qualifications, and how to tailor your resume for this role—all brought to you by Pharmabharat.org, your trusted source for Pharma jobs in India.
Job Overview: Clinical Safety Associate at ProductLife Group
- Location: Remote (India)
This Clinical Safety Associate job offers a chance to work remotely while playing a pivotal role in pharmacovigilance activities. With over 100 applicants already, competition is heating up—don’t miss out! Visit Pharmabharat.org for more Pharmacovigilance jobs in India and career insights.
Key Responsibilities
As a Clinical Safety Associate at ProductLife Group, you’ll contribute to critical safety processes in their hub. Your responsibilities include:
- Processing Adverse Events (AEs), Serious Adverse Events (SAEs), and Suspected Unexpected Serious Adverse Reactions (SUSARs) in the safety database, ensuring timely communication with customers.
- Preparing and following up on queries related to safety data.
- Maintaining study trackers and reconciliation tools.
- Assisting in aggregate periodic safety reports and expedited safety report submissions.
- Collaborating with customers, CROs, and data management teams for seamless safety operations.
These tasks require precision, analytical skills, and a strong understanding of pharmacovigilance regulations—making this an ideal role for experienced professionals in drug safety.
Qualifications and Skills Required
To qualify for this Pharma job, candidates need:
- Education: BSc in Life Sciences or PharmD (or equivalent).
- Experience: Prior experience in pharmacovigilance or drug safety data entry.
- Technical Knowledge: Familiarity with safety databases (e.g., SafetyEasy) and pharmacovigilance tools.
- Regulatory Expertise: Understanding of national and international pharmacovigilance regulations.
- Skills: Analytical mindset, adaptability, good writing skills, and proficiency in MS Office.
If your resume reflects these qualifications, you’re already a strong contender for this Clinical Safety Associate job.