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Bristol Myers Squibb Hiring Clinical Research Associates

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Bristol Myers Squibb

2 - 7 Years

6 - 11 Lacs per anum

Hyderabad

B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences

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Job highlights

Work/Life Balance

Time management

challenging projects

Insurance

Bristol Myers Squibb (BMS) is a global biopharmaceutical company dedicated to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. With a focus on oncology, cardiology, immunology, and neurology, BMS leverages cutting-edge science and technology to deliver transformative therapies. Joining BMS means becoming part of a team that is passionate about making a difference in patients’ lives.

Responsibilities in the Job

As a Clinical Research Associate (CRA) at BMS, you will play a vital role in ensuring the success of clinical trials. Key responsibilities include:

  • Conducting site monitoring visits, including Site Initiation Visits (SIV), Site Monitoring Visits (SMV), and Site Selection Visits (SSV).
  • Managing end-to-end monitoring processes for clinical trials spanning phases 1 to 4.
  • Collaborating with site staff to ensure compliance with regulatory requirements and trial protocols.
  • Ensuring the collection and documentation of high-quality clinical data.
  • Addressing site-specific challenges to maintain timelines and data accuracy.
  • Supporting sites in areas of indication such as immunology, cardiology, oncology, and neurology.

Qualifications

To excel in this role, candidates must meet the following qualifications:

  • A degree in life sciences, pharmacy, or a related field.
  • 2 to 7 years of experience in clinical research.
  • Demonstrated expertise in conducting 30+ site monitoring visits.
  • Hands-on experience across various phases of clinical trials (phase 1 to phase 4).
  • Knowledge of Good Clinical Practice (GCP) and ICH guidelines.

Skills Required

Candidates should possess the following skills to thrive in this position:

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  • Strong expertise in site monitoring activities (SIV, SMV, SSV).
  • In-depth understanding of clinical trial processes and protocols.
  • Exceptional communication and interpersonal skills to build rapport with site staff.
  • Problem-solving capabilities to address site challenges effectively.
  • Knowledge and experience in key therapeutic areas: immunology, cardiology, oncology, and neurology.

How to Apply

Take the next step in your career with this exciting opportunity at Bristol Myers Squibb! Interested candidates are encouraged to submit their resumes to fatima.sufi@iqvia.com. Ensure your application highlights your experience with site monitoring, clinical trials, and your expertise in relevant therapeutic areas.