The whole range of Phase I to IV clinical development services are offered by Parexel, one of the biggest clinical research organisations (CROs) in the world, to assist patients receive life-saving therapies more quickly. Our team of more than 20,000 global professionals collaborates with biopharmaceutical leaders, up-and-coming innovators, and sites to design and deliver clinical trials with patients in mind. By leveraging the depth of our clinical, regulatory, and therapeutic expertise, we can make clinical research a treatment option for anyone, anywhere.
Post Name: Pharmacovigilance
Qualification: M. Pharma/ M. Sc./ BDS/ MDS/ Pharm. D/ M. Tech (Biotechnology)
Location: Work from home
Job roles:
- keeping track of and disclosing adverse reactions obtained from patients and healthcare professionals
- interviewing patients and healthcare professionals in-depth
- acquiring in-depth product knowledge
- submitting recurring reports on the safety of medications and other therapies
- Forms and reports for major adverse effects are written and reviewed.
- highlighting the early warning symptoms of medication side effects
- reducing the possibility of harmful side effects
- carrying out safety audits
- working on new medicine clinical trials
Send Your CV to ajay.kumar2@parexel.com; bharat.mehta@parexel.com; srivyshnavi.kolluri@parexel.com; venkata.giri@parexel.com; and subramanyam.turga@parexel.com
Please send your Cv in PDF fromat between 10am to 2pm by renaming it as CV_first name last name_qualification_fresher
Subject of mail: CV for the post of Drug Safety Associate.
