JOB DESCRIPTION:

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), good 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.
• 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)