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ACM Global Hiring for Study Support Coordinator in Clinical Research

Job Title: Study Support Coordinator

Location: Mumbai, India

About Us:

We are a rapidly expanding organization in the clinical trials and central laboratory sector. We are committed to precision, collaboration, and patient-focused excellence. We offer a dynamic and rewarding environment for individuals looking to build a career in clinical research, study coordination, or healthcare operations.

Job Summary:

We are seeking a highly motivated and detail-oriented Study Support Coordinator to join our team in Mumbai. This role provides a fantastic opportunity to grow within clinical operations and project management, with long-term career potential. The ideal candidate will have a strong scientific background and an interest in clinical data management, study support, compliance, and LIMS systems.

Responsibilities:

  • Participate in Clinical Trial Study Management meetings and cross-functional task forces.
  • Maintain strong working relationships with project stakeholders.
  • Perform LIMS data entry, including sample registration and result entry.
  • Track and process results from reference laboratories and 3PL partners.
  • Communicate with laboratory personnel for authorization of received results.
  • Support study validations, testing workflows, and ensuring test case compliance.
  • Assist Clinical Trial Research Associates with data queries and data cleaning.
  • File documentation and maintain audit-ready study records.
  • Participate in training and stay updated on GCP, ICH, GDP, and regulatory standards.
  • Support project managers with day-to-day operational tasks.
  • Contribute during audits and inspections.
  • Help ensure team productivity, motivation, and alignment with business goals.

Minimum Qualifications:

  • Graduate degree in Biochemistry, Biotechnology, Microbiology, Chemistry, or related scientific streams.
  • Strong written and verbal communication skills.
  • Computer proficiency and ability to work with reporting systems or relational databases.

Preferred Qualifications:

  • Master’s degree in a life science discipline.
  • 1+ year experience in clinical trials, laboratory operations, or healthcare services.
  • Customer service or stakeholder management experience.
  • Ability to manage workload and prioritize efficiently.
  • Strong critical thinking and problem-solving skills.

Employment Details:

  • Mode: Full-time
  • Working Schedule: Monday to Friday
  • Hours Per Week: 40 hours

Salary Range (Estimated):

  • INR 4,20,000 – 7,80,000 per year (Salary may vary based on experience, internal policy, and expertise.)

Benefits:

  • Opportunity to work in global clinical trial operations
  • Training and professional development support
  • Exposure to LIMS, regulatory compliance, GCP & ICH frameworks
  • Growth path toward Clinical Trial Coordinator / Project Associate roles

How to Apply:

If you are a motivated and qualified individual looking for a challenging and rewarding opportunity, we encourage you to apply.