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Research Associate

Lambda Research Accelerated
Lambda Research accelerated
5-7 years
500,000 – 700,000
10 Jan. 12, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Research Associate
Req ID: 1306
Location: Ahmedabad, India
Company: Lambda Therapeutic Research Ltd.
CTC Range: INR 500,000 – 700,000

Organizational Overview:
Lambda Therapeutic Research Ltd. is a global full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India. With strategically located facilities in Mehsana (India), Las Vegas (USA), Toronto (Canada), Barcelona (Spain), London (UK), and Warsaw (Poland), we provide end-to-end clinical research solutions to innovators, biotech companies, and generic pharmaceutical industries worldwide.

Position Overview:
We are seeking an experienced Research Associate to join our clinical operations team. The ideal candidate will play a key role in volunteer recruitment, data management, and study coordination, ensuring high-quality execution of clinical trials in compliance with regulatory standards.

Key Responsibilities:

  • Maintain and enhance the volunteer databank to ensure a robust pool of study participants.

  • Conduct tele-calling and field visits for volunteer recruitment and screening.

  • Ensure adequate number of eligible subjects are recruited and available for clinical trials.

  • Coordinate effectively between project coordinators, subjects, and study teams.

  • Verify laboratory reports against requisitions and ensure data accuracy.

  • Complete, compile, and review Master Screening Records (MSRs), consent forms for screening, and Participant Information Forms (PIFs).

  • Prepare identification cards and index cards for study participants.

  • Conduct post-study follow-up activities to ensure participant safety and study integrity.

  • Participate in project-related activities and support the department in achieving operational goals.

  • Perform additional responsibilities assigned by the Head of Department.

Experience Required:

  • 5 to 7 years of experience in clinical research operations, volunteer recruitment, or related roles.

Educational Qualification:

  • Any Graduate degree from a recognized institution.

Why Join Lambda Therapeutic Research:

  • Opportunity to work with a global CRO with multi-country operations.

  • Exposure to end-to-end clinical research processes, including volunteer management and data coordination.

  • Professional development and career growth in a collaborative and high-performance environment.