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Clinical Trial Manager

On-site EPD, India full time

JOB DESCRIPTION:

Main Purpose of the Role

  • Summarize the main purpose of the role Individual contributor with comprehensive knowledge in specific area.
    Ability to execute highly complex or specialized projects.
    Adapts precedent and may make significant departures from traditional approaches to develop solutions.

Main Responsibilities

  • List the main responsibilities this role regularly performs. Processes, reviews, and receives patient data and records and organizes clinical data forms from particular therapeutic groups and outside investigators. Provides accurate, timely, and consistent clinical data to the medical department and other groups. Responsible for data management plans including data preparation, data validation activities, etc. Follows Good Clinical Practices (GCP) data-handling procedures and guidelines. Requires knowledge of drug and disease terminology. May manage service providers that perform these activities. Participates in the review of clinical research protocols, reports and statistical analysis plans.

The base pay for this position is

N/A

In specific locations, the pay range may vary from the range posted.

JOB FAMILY:

Clinical Affairs / Statistics

DIVISION:

EPD Established Pharma

LOCATION:

India > Mumbai : Mumbai Development Center - EPD

ADDITIONAL LOCATIONS:

WORK SHIFT:

Standard

TRAVEL:

Not specified

MEDICAL SURVEILLANCE:

Not Applicable

SIGNIFICANT WORK ACTIVITIES:

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

Source: the employer's careers page. Last checked 2026-10-23. Posted 2026-10-19.

Applications happen on Abbott's own site. View role and apply

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