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Senior Manager Medical Affairs @ Abbott

Mumbai, Maharashtra, INOnsiteFull-time
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About this role

JOB DESCRIPTION

MAIN PURPOSE OF THE ROLE

Leads/supervises a team of more than 2 professionals within the Medical Affairs Sub-Function.

First level manager of a work team that may comprise professionals, technical and/or administrative staff.

Typically without budget or hire/fire authority.

Focuses on mentoring, coaching, and coordination.

MAIN RESPONSIBILITIES

  • As the Supervisor of the Medical Affairs Sub-Function, supervises professionals 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.
  • Coordinates and oversees investigator initiations and group studies.
  • May participate in adverse event reporting and safety responsibilities monitoring.
  • May act as consultant/liaison with other corporations when working under licensing agreements.

QUALIFICATIONS

Education Level Major/Field of Study or Equivalent

Associates Degree (± 13 years)

Experience/Background

Minimum 4 years

The base pay for this position is

N/AIn specific locations, the pay range may vary from the range posted.

JOB FAMILY

Medical & Scientific Affairs

DIVISION

EPD Established Pharma

LOCATION

India > Mumbai : BKC Building

ADDITIONAL LOCATIONS

WORK SHIFT

Standard

TRAVEL

Not specified

MEDICAL SURVEILLANCE

Not Applicable

SIGNIFICANT WORK ACTIVITIES

Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)

Skills

clinical trialstudy designadverse event reportinghuman clinical trialsData Collectionprotocol adherencegroup studieslicensing agreementsMentoringCoaching

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