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Manager

Lambda Research Accelerated
Lambda Research accelerated
2-3 years
INR 8–15 LPA
Ahmedabad, Gujarat, India
10 March 24, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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

Manager – Clinical Research (Study Physician / Co-Investigator)

Location: Ahmedabad, Gujarat, India
Job Type: Full-Time
Industry: Clinical Research / CRO
Company: Lambda Therapeutic Research Ltd.
Experience Required: 2–3 years
Salary Range: INR 8–15 LPA

Job Overview
Lambda Therapeutic Research Ltd., a leading global Contract Research Organization (CRO), is seeking a qualified Manager – Clinical Research (Study Physician / Co-Investigator) to support and oversee clinical trial activities. This role involves conducting medical evaluations, ensuring subject safety, managing clinical study protocols, and maintaining regulatory compliance. The position is ideal for medical professionals looking to build a career in clinical research with hands-on exposure to trials and patient safety management.

Key Responsibilities
Act as a Co-Investigator and Study Physician for clinical trials, ensuring adherence to study protocols and regulatory guidelines. Conduct clinical examinations and assess subject eligibility for participation in clinical studies. Lead volunteer screening and recruitment processes in coordination with relevant teams. Monitor, evaluate, and manage adverse events, ensuring appropriate documentation and timely follow-up.

Coordinate with Institutional Ethics Committees (IEC) and communicate study-related updates and issues to stakeholders. Prepare and review clinical study protocols, reports, and medical documentation. Ensure strict compliance with SOPs, regulatory requirements, and study protocols throughout the trial lifecycle. Collaborate with project coordinators and cross-functional teams to ensure smooth execution of clinical studies.

Train and guide contractual staff on study-related procedures and maintain accurate training records. Handle medical confidentiality, case management, and safety-related communications with sponsors and internal teams. Support quality assurance activities, respond to audit findings, and contribute to continuous improvement of systems and SOPs.

Eligibility Criteria
Candidates must hold an MBBS degree from a recognized institution. A minimum of 2–3 years of relevant experience in clinical research, clinical practice, or as a study physician is required.

Required Skills and Competencies
Strong understanding of clinical research processes, GCP guidelines, and regulatory requirements. Experience in subject screening, clinical assessments, and adverse event management. Excellent communication and stakeholder coordination skills. Strong attention to detail and ability to maintain accurate medical documentation. Ability to work in a fast-paced clinical research environment while ensuring patient safety and data integrity.

Why Join Lambda Therapeutic Research Ltd.
Lambda Therapeutic Research offers a dynamic environment with exposure to global clinical trials and end-to-end research services. Employees benefit from structured career growth, hands-on clinical experience, and the opportunity to work with international sponsors and multidisciplinary teams.

Equal Opportunity Statement
Lambda Therapeutic Research Ltd. is an equal opportunity employer committed to diversity, inclusion, and fair employment practices. All qualified applicants will be considered based on merit and organizational needs.

This role is ideal for MBBS professionals seeking to transition or advance in clinical research as a Study Physician or Co-Investigator within a globally recognized CRO.