Posted:
8/18/2025, 5:48:54 PM
Location(s):
Maharashtra, India ⋅ Mumbai, Maharashtra, India
Experience Level(s):
Junior ⋅ Mid Level
Field(s):
Medical, Clinical & Veterinary
MAIN PURPOSE OF ROLE
MAIN RESPONSIBILITIES
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As the Experienced professional in the Medical Affairs Sub-Function, possesses well developed skills in overseeing the direction, planning, execution, clinical trials/research and the data collection activities.
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Contributes to implementation of clinical protocols, and facilitates completion of final reports.
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Recruits clinical investigators and negotiates study design and costs.
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Responsible for directing human clinical trials, phases III & IV for company products under development.
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Participates in adverse event reporting and safety responsibilities monitoring.
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Coordinates and provides reporting information for reports submitted to the regulatory agencies.
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Monitors adherence to protocols and determines study completion.
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Coordinates and oversees investigator initiations and group studies.
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May participate in adverse event reporting and safety responsibilities monitoring.
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May act as consultant/liaison with other corporations when working under licensing agreements.
Education
Education Level: Associates Degree (± 13 years)
Experience/Background
Experience: Minimum 1 year
The base pay for this position is
N/AIn specific locations, the pay range may vary from the range posted.
Website: https://abbott.com/
Headquarter Location: Illinois City, Illinois, United States
Employee Count: 1001-5000
Year Founded: 1944
IPO Status: Public
Last Funding Type: Post-IPO Debt
Industries: Biotechnology ⋅ Emergency Medicine ⋅ Genetics ⋅ Health Care ⋅ Health Diagnostics ⋅ Manufacturing ⋅ Medical ⋅ Medical Device ⋅ Nutrition ⋅ Pharmaceutical