you will be responsible for overseeing the safety evaluation of our pharmaceutical products and ensuring compliance with regulatory requirements. You will work closely with cross-functional teams to drive drug safety initiatives, enhance patient safety, and contribute to the overall success of our product portfolio.
Responsibilities:
Ensure compliance with regulatory requirements for adverse event reporting and safety data management
Oversee the preparation and submission of safety reports and regulatory documents to health authorities
Develop and implement risk management plans and strategies to mitigate safety risks associated with our products
Collaborate with clinical development, regulatory affairs, and marketing teams to ensure safety considerations are integrated throughout the product lifecycle
Provide expert guidance on safety-related issues during internal and external audits
Monitor industry trends and regulatory changes, adapting processes and policies as necessary
Foster a culture of safety within the organization, promoting education and awareness of drug safety issues
Requirements:
BCA,MCA,Bsc.IT,Msc.IT,IT,Diploma,B.Tech,M.Tech.
M.D., Ph.D., or Pharm.D. with a focus in pharmacology, toxicology, or related field
Skills-Proven ability to lead cross-functional teams and drive projects to successful completion
Other Details
Sallary-29K To 48K
Experience:-0 To 4 Years
Minimum Age-18+
Work Department-Pharmacovigilance
Work Industry-Pharma,Healthcare,
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Best Regards
HR TEAM
Keyskills: reporting