SESeven Consultancy
Drug Safety Associate
Bangalore ₹4-7 LPA Posted 12 Dec 2025
FULL TIME
Gcp
Fda
Case Processing
Drug Safety
Clinical Research
Job Description
- Ensure that safety reports received from investigational sites or post-marketing sectors are identified and reported in accordance with ICH-GCP standards and standard operational procedures.
- Organize collected reports based on the seriousness or effectiveness of the drug.
- Maintain consistency in assessing adverse reaction reports accurately and legibly.
- Apply knowledge of FDA and ICH-GCP regulations to make appropriate decisions.
- Communicate effectively with clinical physicians regarding drug safety and assess case report forms.
- Distinguish and analyze the ratio of risks and benefits of marketed drugs.