Clinical Trial Associate Opportunity in Mumbai – Bristol Myers Squibb

Clinical Trial Associate Vacancies at Bristol Myers Squibb

About the Company (Bristol Myers Squibb)

Welcome to Bristol Myers Squibb, where the extraordinary happens daily. Our commitment goes beyond the ordinary, as we strive to make a meaningful impact on patients’ lives. At Bristol Myers Squibb, we embrace diverse and challenging work that transforms careers and directly influences patient outcomes. If you’re looking for a career that is both challenging and meaningful, you’re in the right place.

Bristol Myers Squibb Vacancies List

Position Title: Clinical Trial Associate

Company Name: Bristol Myers Squibb

Job Category: Clinical Development

Job ID: R1576538

Job Location: Mumbai, India

Employment Type: Full Time

Job Description

About the Department & Responsibilities

Purpose/Objective of the Job: This position involves managing administrative and business activities related to the conduct of clinical trials from study start-up to study closure.

Key Responsibilities:

1. Set up vendors during the study start-up period.
2. Enter necessary data/tracking in systems (CTMS, eTMF, SAP).
3. Manage documentation within the electronic master file and other systems.
4. Coordinate the importation of drugs and non-drug items to support study sites.
5. Complete payment activities, including preparing invoices and creating fund/PO.
6. Coordinate study-related materials for translation.
7. Provide administrative support to the study team.
8. Obtain insurance certificates.
9. Support equipment calibration and tracking.
10. Handle archiving processes at study closure.

Qualification and Experience:

• Bachelor’s degree within Life Sciences area, Administrative, Financial, or Accounting related field preferred, or minimum 2 years of working experience in any of these areas in addition to a high school degree or local equivalent.
• 1 – 3 years’ experience in Clinical Research or related work experience.
• Experience in the use of industry Clinical Trial Management Systems and Clinical Trial Master File Systems or equivalent preferred.

Competencies:

• Basic understanding of GCPs, ICH Guidelines, and local regulations.
• Basic knowledge of the drug development process in relation to the execution of clinical trials.
• Experience in managing multiple priorities and accomplishing tasks within set timeframes.
• Demonstrates the ability to function independently.
• General knowledge of software systems and web-based applications.
• Good verbal and written communication skills (both in English and local language).

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