Opening for Drug Safety Specialist (GPIO) @ Parexel
PAREXEL has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis. As a leading global biopharmaceutical service provider, they supply knowledge-based contract research, medical communications and consulting services across a broad range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries. They have helped over 800 clients to develop and launch some of the most important drugs and devices of our time-helping people live better and healthier lives everywhere in the world. Headquartered near Boston, Massachusetts, PAREXEL operates in more than 50 countries around the world.
Post: Drug Safety Specialist (GPIO)
Job Description
The Drug Safety Specialist will provide technical, process-related and administrative support to drug safety management and medical monitoring activities, regulatory information collection and organization, regulatory reporting, and medical project management activities.
For members of the Global Pharmacovigilance Information Office (GPIO):
- Support collection and organization of global PV requirements
- Data entry and maintenance of country specific requirements in PAREXEL’s PV repository
- Receipt and triage of requests for updates to country requirements
- Communicate country-specific regulatory updates to project teams as required
- Maintain updated network list of Named Safety Contacts/LQPPV
- Work directly with relevant stakeholders on standalone GPIO projects
Candidate Profile
Related experience gained in a healthcare environment is an advantage.
Fluent in spoken and written English.
Additional Information:
Location: Telangana - Hyderabad
Functional Area: Medical Affairs
Requisition: pare-10042116
Industry Type: Pharma/ Biotech/Clinical Research
Employment Type: Full Time
Job Type: Regular
End Date: 30th April, 2015
Click here to apply
PAREXEL has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis. As a leading global biopharmaceutical service provider, they supply knowledge-based contract research, medical communications and consulting services across a broad range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries. They have helped over 800 clients to develop and launch some of the most important drugs and devices of our time-helping people live better and healthier lives everywhere in the world. Headquartered near Boston, Massachusetts, PAREXEL operates in more than 50 countries around the world.
Post: Drug Safety Specialist (GPIO)
Job Description
The Drug Safety Specialist will provide technical, process-related and administrative support to drug safety management and medical monitoring activities, regulatory information collection and organization, regulatory reporting, and medical project management activities.
For members of the Global Pharmacovigilance Information Office (GPIO):
- Support collection and organization of global PV requirements
- Data entry and maintenance of country specific requirements in PAREXEL’s PV repository
- Receipt and triage of requests for updates to country requirements
- Communicate country-specific regulatory updates to project teams as required
- Maintain updated network list of Named Safety Contacts/LQPPV
- Work directly with relevant stakeholders on standalone GPIO projects
Candidate Profile
Related experience gained in a healthcare environment is an advantage.
Fluent in spoken and written English.
Additional Information:
Location: Telangana - Hyderabad
Functional Area: Medical Affairs
Requisition: pare-10042116
Industry Type: Pharma/ Biotech/Clinical Research
Employment Type: Full Time
Job Type: Regular
End Date: 30th April, 2015
Click here to apply
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