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Manager

Lambda Research Accelerated
Lambda Research accelerated
2-3 years
₹8,00,000 – ₹15,00,000 per year
Ahmedabad, India
10 March 10, 2026
Job Description
Job Type: Full Time Education: MBBS 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: Manager (Clinical Research)

Company: Lambda Therapeutic Research Ltd.

Location: Ahmedabad, India

Req ID: 1468

Date Posted: Feb 19, 2026

Salary (CTC): ₹8,00,000 – ₹15,00,000 per year

Category: Clinical Research / Medical Affairs


Job Overview

The Manager will function as a Co-Investigator and Study Physician responsible for overseeing medical aspects of clinical studies. The role includes screening and recruitment of volunteers, conducting clinical assessments, ensuring compliance with study protocols and regulatory requirements, and managing safety and adverse event reporting. The position requires coordination with project teams, sponsors, and regulatory bodies to ensure successful execution of clinical trials.


Key Responsibilities

  • Act as a Co-Investigator / Study Physician for assigned clinical studies.

  • Perform medical screening and recruitment of volunteers for clinical trials.

  • Conduct clinical examinations and determine eligibility of study participants.

  • Train and guide contractual staff involved in study-related activities and maintain training records.

  • Coordinate with volunteer recruitment and screening teams regarding adverse events and follow-ups.

  • Prepare and review clinical study protocols and ensure adherence during study execution.

  • Coordinate activities related to Institutional Ethics Committee (IEC) submissions and approvals.

  • Ensure compliance with study protocols, SOPs, and regulatory requirements.

  • Collaborate with Project Coordinators on study planning, execution, and reporting.

  • Monitor and manage adverse events and safety-related issues during studies.

  • Ensure timely response and resolution of QA findings.

  • Interact with study sponsors regarding medical and safety-related matters.

  • Prepare and review clinical study reports and documentation.

  • Manage confidential medical records and case documentation.

  • Support the maintenance and updating of departmental systems and SOPs.

  • Perform additional responsibilities as assigned by management or department leadership.


Required Skills & Competencies

  • Strong understanding of clinical trial processes and medical monitoring.

  • Knowledge of GCP guidelines, regulatory requirements, and ethical standards in clinical research.

  • Ability to manage participant screening, safety monitoring, and adverse event reporting.

  • Excellent communication and coordination skills for working with cross-functional teams and sponsors.

  • Strong documentation and reporting skills for clinical study records.

  • Ability to maintain medical confidentiality and regulatory compliance.


Experience

  • 2–3 years of relevant experience in clinical research or medical practice, preferably within a Clinical Research Organization (CRO) or hospital setting.


Educational Qualification

  • M.B.B.S. (Bachelor of Medicine and Bachelor of Surgery).