Posted:4 weeks ago|
Platform:
On-site
Full Time
Responsibilities: Collect and process adverse event reports from clinical trials and post-marketing sources Perform case triage, data entry, and quality checks in safety databases Assist in preparation of regulatory reports (e.g., CIOMS, MedWatch) Conduct literature screening for safety data Ensure compliance with global pharmacovigilance regulations and SOPs Job Types: Full-time, Fresher Pay: ₹286,000.00 - ₹970,000.00 per year Benefits: Health insurance Schedule: Day shift Work Location: In person
Fusion Technology Solutions
Upload Resume
Drag or click to upload
Your data is secure with us, protected by advanced encryption.
Browse through a variety of job opportunities tailored to your skills and preferences. Filter by location, experience, salary, and more to find your perfect fit.
We have sent an OTP to your contact. Please enter it below to verify.
Instantly access job listings, apply easily, and track applications.
Hyderabad, Bengaluru, Mumbai (All Areas)
Experience: Not specified
0.6 - 0.7 Lacs P.A.
Mumbai, Maharashtra, India
Experience: Not specified
Salary: Not disclosed
Hyderabad
5.0 - 8.0 Lacs P.A.
Satara, Maharashtra
Experience: Not specified
2.86 - 9.7 Lacs P.A.
Mumbai, Maharashtra, India
Experience: Not specified
Salary: Not disclosed
Satara, Maharashtra
Experience: Not specified
2.86 - 9.7 Lacs P.A.
