...responsibility of this position relies on Managing the Department including coaching/mentoring/training/support of direct reports and development plan... .... An educational background as a B...
...Responsibilities :-
Processing of Individual Case Safety Reports from all sources (post-marketing and clinical trials, including device and combination products) in compliance with applicable regulations, PrimeV...
...Clinical Research Associate
Job Requirements Techno Endura Is Offering Internship, For Pharmacy Medical & LifeScience Grads On Live Projects & Clinical Software and Will support Job In Clinica...
...procedures
Conduct risk-benefit assessments of pharmaceutical products
Stay up-to-date on the latest pharmacovigilance regulations and guidance
Qualifications
~ Bachelor's degree in a related field, such ...
...We're seeking highly motivated and self-starting individuals to join our diverse and very engaged quality auditing team! We offer a quality auditing function, with good visibility into our Research & Development fun...
...Job Description :
1) Should be a medical doctor - preferably with MD in Pharmacology
2) 4+ years- experience in handling Phase 2/Phase 3 clinical trials in India
3) Manage the CRO team for all clinical ...
Pharmacovigilance Associate- Freshers
Essential Duties and Responsibilities
Collect and evaluate adverse event reports from various sources, including healthcare professionals, patients, and drug company representatives
Assess the severit...
The Pharmacovigilance (PV) Physician II is responsible for medical review of ICSRs and literature review, writing signal detection reports, supporting writing and or reviewing of aggregate reports (DSURS, PSURS, PBRERs, PADERS).
To review and app...
...You will be expected to develop and review complex edit checks, patient profile listings, reports, preprocessing checks & map datasets for validation based on study requirements using different tools/techs such as Cognos / SAS, ...
...Pharmacovigilance Associate- Freshers
Essential Duties and Responsibilities
Collect and evaluate adverse event reports from various sources, including healthcare professionals, patients, and drug company rep...
