:

MAIN PURPOSE OF THE ROLE

Individual contributor that works under limited supervision.

Applies subject matter knowledge.

Requires capacity to understand specific needs or requirements to apply skills/knowledge.

MAIN RESPONSIBILITIES

. Plans, directs, creates and communicates clinical study time-lines.

. Gathers input from cross-functional teams and creates plans that help the team produce deliverables on schedule.

. Ensures consistency of clinical study and processes across clinical trials.

. Oversees and resolves operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), positive clinical practice (GCP) and specific country regulations such as site and vendor selection, preparing clinical trial budgets.

. Ensures study is conducted within clinical trial protocols.

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Monitors progress and follows up with team members and line managers when issues develop.

QUALIFICATIONS

Education Level Major/Field of Study or Equivalent

Associates Degree (± 13 years)

Experience/Background

Minimum 1 year 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:

MD Medical Devices

LOCATION:

India Gurgaon : BPTP Park Centra

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)

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