Posted:1 day ago|
Platform:
On-site
Full Time
MAIN PURPOSE OF ROLE
Experienced professional individual contributor that works under limited supervision.
Applies subject matter knowledge in the area of Medical Affairs.
Requires capacity to apply skills/knowledge within the context of specific needs or requirements.
MAIN RESPONSIBILITIES
.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.
.Contributes to implementation of clinical protocols, and facilitates completion of final reports.
.Recruits clinical investigators and negotiates study design and costs.
.Responsible for directing human clinical trials, phases III & IV for company products under
development.
.Participates in adverse event reporting and safety responsibilities monitoring.
.Coordinates and provides reporting information for reports submitted to the regulatory agencies.
.Monitors adherence to protocols and determines study completion.
The base pay for this position is
N/AIn specific locations, the pay range may vary from the range posted.
Abbott Healthcare
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