Manager – Clinical Research (Study Physician / Co-Investigator)
Location: Ahmedabad, India
Company: Lambda Therapeutic Research Ltd.
CTC Range: INR 8,00,000 – 15,00,000 per annum
Employment Type: Full-Time
Job Overview
Lambda Therapeutic Research Ltd. is seeking a qualified medical professional for the role of Manager – Clinical Research (Study Physician / Co-Investigator). This position involves overseeing clinical trial activities, ensuring subject safety, and maintaining compliance with regulatory and ethical standards. The ideal candidate will play a key role in study execution, volunteer management, and clinical oversight within a dynamic CRO environment.
Key Responsibilities
Clinical Trial Execution & Medical Oversight
Act as Co-Investigator/Study Physician for clinical trials
Conduct clinical examinations and assess subject eligibility as per study protocols
Oversee volunteer recruitment and screening processes
Monitor and manage Adverse Events (AEs) and ensure appropriate follow-up and reporting
Protocol & Documentation Management
Prepare and review clinical study protocols and study-related documentation
Maintain accurate medical records, case reports, and confidential subject data
Ensure timely preparation and review of clinical study reports
Regulatory & Compliance Management
Ensure compliance with Good Clinical Practice (GCP), SOPs, and regulatory requirements
Coordinate with Institutional Ethics Committees (IEC) for approvals and updates
Address quality assurance findings and ensure timely resolution
Team Coordination & Training
Train and guide contractual staff on study-related procedures and maintain training records
Collaborate with project coordinators and cross-functional teams for smooth study execution
Communicate effectively with sponsors on medical and study-related matters
Safety & Risk Management
Handle safety-related issues and ensure proper documentation and communication
Monitor ongoing subject health and manage clinical risks throughout the study lifecycle
Process Improvement & Documentation
Support the development and updating of departmental SOPs and systems
Contribute to continuous improvement initiatives in clinical research processes
Required Qualifications
MBBS (Bachelor of Medicine and Bachelor of Surgery)
Strong understanding of clinical trial processes, GCP guidelines, and regulatory requirements
Good clinical judgment and patient management skills
Experience Required
2–3 years of relevant experience in clinical research or healthcare
Experience as a Study Physician or Co-Investigator in clinical trials is preferred
Hands-on experience in subject screening, safety monitoring, and protocol compliance
Key Skills
Clinical Trial Management
Patient Screening & Medical Assessment
Adverse Event (AE) Management
Protocol Review & Compliance
Regulatory & Ethics Coordination (IEC)
Documentation & Reporting
Team Training & Collaboration
Why Join Lambda Therapeutic Research?
Be part of a globally recognized CRO with international operations
Gain exposure to diverse clinical trials and therapeutic areas
Collaborative and research-driven work environment
Opportunities for professional growth and advancement
About Lambda Therapeutic Research Ltd.
Lambda Therapeutic Research Ltd. is a global full-service Contract Research Organization (CRO) headquartered in Ahmedabad, India, providing end-to-end clinical research services to pharmaceutical, biotechnology, and generic drug companies worldwide.
How to Apply
Interested candidates can apply through the official company careers portal or submit their updated resume via ThePharmaDaily.com to explore opportunities in clinical research and medical roles.
Manager – Clinical Research (Study Physician / Co-Investigator)
Location: Ahmedabad, India
Company: Lambda Therapeutic Research Ltd.
CTC Range: INR 8,00,000 – 15,00,000 per annum
Employment Type: Full-Time
Job Overview
Lambda Therapeutic Research Ltd. is seeking a qualified medical professional for the role of Manager – Clinical Research (Study Physician / Co-Investigator). This position involves overseeing clinical trial activities, ensuring subject safety, and maintaining compliance with regulatory and ethical standards. The ideal candidate will play a key role in study execution, volunteer management, and clinical oversight within a dynamic CRO environment.
Key Responsibilities
Clinical Trial Execution & Medical Oversight
Act as Co-Investigator/Study Physician for clinical trials
Conduct clinical examinations and assess subject eligibility as per study protocols
Oversee volunteer recruitment and screening processes
Monitor and manage Adverse Events (AEs) and ensure appropriate follow-up and reporting
Protocol & Documentation Management
Prepare and review clinical study protocols and study-related documentation
Maintain accurate medical records, case reports, and confidential subject data
Ensure timely preparation and review of clinical study reports
Regulatory & Compliance Management
Ensure compliance with Good Clinical Practice (GCP), SOPs, and regulatory requirements
Coordinate with Institutional Ethics Committees (IEC) for approvals and updates
Address quality assurance findings and ensure timely resolution
Team Coordination & Training
Train and guide contractual staff on study-related procedures and maintain training records
Collaborate with project coordinators and cross-functional teams for smooth study execution
Communicate effectively with sponsors on medical and study-related matters
Safety & Risk Management
Handle safety-related issues and ensure proper documentation and communication
Monitor ongoing subject health and manage clinical risks throughout the study lifecycle
Process Improvement & Documentation
Support the development and updating of departmental SOPs and systems
Contribute to continuous improvement initiatives in clinical research processes
Required Qualifications
MBBS (Bachelor of Medicine and Bachelor of Surgery)
Strong understanding of clinical trial processes, GCP guidelines, and regulatory requirements
Good clinical judgment and patient management skills
Experience Required
2–3 years of relevant experience in clinical research or healthcare
Experience as a Study Physician or Co-Investigator in clinical trials is preferred
Hands-on experience in subject screening, safety monitoring, and protocol compliance
Key Skills
Clinical Trial Management
Patient Screening & Medical Assessment
Adverse Event (AE) Management
Protocol Review & Compliance
Regulatory & Ethics Coordination (IEC)
Documentation & Reporting
Team Training & Collaboration
Why Join Lambda Therapeutic Research?
Be part of a globally recognized CRO with international operations
Gain exposure to diverse clinical trials and therapeutic areas
Collaborative and research-driven work environment
Opportunities for professional growth and advancement
About Lambda Therapeutic Research Ltd.
Lambda Therapeutic Research Ltd. is a global full-service Contract Research Organization (CRO) headquartered in Ahmedabad, India, providing end-to-end clinical research services to pharmaceutical, biotechnology, and generic drug companies worldwide.
How to Apply
Interested candidates can apply through the official company careers portal or submit their updated resume via ThePharmaDaily.com to explore opportunities in clinical research and medical roles.
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