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Job highlights

Work/Life Balance

Time management

challenging projects

Insurance

Job 1: Specialist, Study Start-up

Job Title: Specialist, Study Start-up
Location: Mumbai, India
Type: Full-time

About Us:

Bristol Myers Squibb is a leading pharmaceutical company that transforms patients’ lives through science. We’re looking for a talented Specialist, Study Start-up to join our team!

Job Description:

We’re seeking a highly motivated and organized individual to lead study start-up activities and ensure successful recruitment and delivery to trial milestones. As a Specialist, Study Start-up, you will:

  • Manage study and site level deliverables during start-up and maintenance
  • Plan and develop strategies for start-up activities
  • Prepare Investigator Sites to conduct clinical trials
  • Support local regulatory in preparing and performing submissions for Health Authorities
  • Collaborate with internal and external stakeholders to ensure tasks and priorities are aligned to defined study timelines

Requirements:

  • Bachelor’s degree in Life Sciences or equivalent
  • 2+ years of industry-related experience
  • Strong organizational and planning skills
  • Ability to communicate effectively in English and local language

What We Offer:

Competitive salary and benefits package
Opportunity to work on high-impact clinical trials
Collaborative and dynamic work environment

Job 2: Clinical Trial Monitor

Job Title: Clinical Trial Monitor
Location: Mumbai, India
Type: Full-time

About Us:

Bristol Myers Squibb is a leading pharmaceutical company that transforms patients’ lives through science. We’re looking for a talented Clinical Trial Monitor to join our team!

Job Description:

We’re seeking a highly motivated and organized individual to oversee the progress of clinical trials and ensure they are conducted, recorded, and reported in accordance with protocol, SOPs, GCP, and regulatory requirements. As a Clinical Trial Monitor, you will:

  • Conduct site visits to monitor trial progress
  • Ensure compliance with regulations and guidelines
  • Collaborate with sites to resolve issues and implement corrective actions
  • Prepare and submit written reports

Requirements:

  • Bachelor’s degree in Life Sciences or equivalent
  • 2-3 years of clinical research experience
  • Strong analytical and problem-solving skills

What We Offer:

Competitive salary and benefits package
Opportunity to work on high-impact clinical trials
Collaborative and dynamic work environment

Application Link For Study Startup Specialist

Application Link for Clinical Trial Monitor

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