Drug Safety Associate Jobs

Tata Consultancy Services - Pune, Maharashtra, India

Qualification - Registered Nurse/ Licensed Practical Nurse/ Pharmacist or Life Science Graduates/ BDS/ BHMS/ BAMS/ MBBS can apply. *Be fully competent to perform all steps within the case-handling processing...

from: linkedin.com - 15 days ago

Novo Nordisk - Bangalore, Karn, IN

a growing team, working in an international environment. The Position A Senior Drug Safety Associate will perform initial evaluation of reported adverse events (serious and non-serious) from all sources

from: Novo Nordisk (+1 source) - 16 days ago

Pharmazone - Ahmedabad, IN

with Regulatory Affairs to ensure appropriate reporting of pharmacovigilance and drug safety information to regulatory agencies and prescriber community. Serves as a subject matter expert for vendors providing drug 300000 - 500000 per year

from: expertia.ai (+1 source) - More than 30 days ago

EDGEPHARMA PVT. LTD. - Mumbai (All Areas)

Summary: The Pharmacovigilance Associate assists with the collection, recording, and reporting of adverse events associated with medications. This role contributes to patient safety by monitoring Not disclosed INR

from: naukri.com - 21 days ago

Clinilaunch Research Institute Llp - Bengaluru / Bangalore, India

This is a full-time on-site role in Bengaluru for a Drug Safety Associate. The Drug Safety Associate will be responsible for tasks such as Reviewing safety data, writing narratives, performing Not Mentioned

from: Monsterindia.com - More than 30 days ago

Sitero - India

and pharmacovigilance services. Training and mentoring of Pharmacovigilance Associates EDUCATION AND EXPERIENCE REQUIRED: Minimum 1+ year of experience in drug safety or clinical research domain Degree in Life Science Not Mentioned

from: Monsterindia.com - More than 30 days ago

Sitero - India

Senior Drug Safety Associate MICC is a safety professional responsible for assessing the safety of pharmaceutical drugs undergoing clinical trials or once they are in the market. Using standard Not Mentioned

from: Monsterindia.com - More than 30 days ago

Novartis - Hyderabad / Secunderabad, Telangana, India

of single case reports. Good fluency in English. Knowledge of other languages desirable. 3+ years of PV or Clinical Drug Development experience post MBBS. Experience in safety document or medical writing Not Mentioned

from: Monsterindia.com - More than 30 days ago

EVERSANA - India

projects. · May work with client Clinical Research, sometimes in a lead capacity, regarding Safety Data Exchange Agreements (SDEA). · Lead team members, e.g., Drug Safety Coordinators, Drug Safety Associates Not Mentioned

from: Monsterindia.com - More than 30 days ago

Sitero - India

into the global drug safety database Perform peer review QC of abstracts. Accessing EV on daily basis and downloading MLM search and MLM ICSR results (excel spreadsheets) Tracking all the MLM search results, MLM Not Mentioned

from: Monsterindia.com - More than 30 days ago