Pharmacovigilance Associate jobs in Bhubaneswar - clinstinct clinical research

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  • Job View 17 Views
  • Applicants Less than 5 Applicants
  • 2019-04-05

Job Description

Job Summary

A pharmacovigilance officer may also be called a drug safety officer. They are responsible for monitoring and reporting the effectiveness and any adverse effects or side effects of pharmaceutical products on the market in the general population and in hospitals and research trials. They must liaise closely with medical and drug company representatives, patients, doctors and other healthcare professionals to record the effectiveness of drugs and other treatments.

Responsibilities and Duties

Responsibilities include:

recording and reporting adverse reactions received from healthcare professionals and consumers

conducting in-depth interviews with patients and healthcare professionals

developing a thorough knowledge of products

completing periodic safety update reports on drugs and other treatments

writing and reviewing serious adverse effects reports and forms

flagging up early warning signs of adverse effects of drugs

Industry

Pharma/BioTech/Clinical Research

Functional Area

Pharma / R&D / Biotech

Number of Vacancy

1

Education

BDS, BHM, B.Pharma, M.Pharma, M.Sc


About clinstinct clinical research

The Clinical Research Coordinator (CRC) is responsible for the coordination and administration
of clinical trials under the direction of the Clinical Research Manager, the Principal Investigator
and the Medical Director. The CRC will develop, implement, and coordinate research and
administrative procedures for the successful management of clinical trials. The CRC will perform
diverse administrative duties requiring analysis, sound judgment, and a high level of knowledge
of study specific protocols.
DUTIES AND RESPONSIBILITIES
Administratively and clinically manage an average of six to eight clinical trials
Adhere to Research SOP’s
Adhere to Good Clinical Practices and the study protocols
Ensure scientific integrity of data and protect the rights, safety, and well-being of patients
enrolled in clinical trials
Discuss study protocols with patients and verify the informed consent documentation
Provide patient with written communication of their participation (i.e. copy of the signed
informed consent)
Ensure patient’s referring physician receives notification of patient’s participation in
studies as requested by the patient
Meet with patient for each visit and maintain accessibility to discuss any
questions/concerns regarding the study
Dispense study medication in a professional and accountable manner following protocol
requirements

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