Senior Manager – Investigator & Physicians | Clinical Research Operations
Location: Ahmedabad, India
Company: Lambda Therapeutic Research Ltd.
CTC Range: INR 12,00,000 – 18,00,000 per annum
Employment Type: Full-Time
Job Overview
Lambda Therapeutic Research Ltd. is seeking a highly qualified Senior Manager – Investigator & Physicians to lead clinical research activities and ensure the successful execution of clinical studies. This role is critical in overseeing protocol compliance, managing study teams, and ensuring adherence to regulatory and ethical standards. The ideal candidate will bring strong medical expertise, leadership capabilities, and hands-on experience in clinical trial conduct within a CRO or pharmaceutical environment.
Key Responsibilities
Clinical Study Oversight & Execution
Conduct feasibility assessments for clinical studies based on sponsor requirements and molecule profiles
Review clinical study protocols to ensure scientific and regulatory alignment
Act as Principal Investigator/Medical Lead to ensure strict adherence to inclusion/exclusion criteria and protocol compliance
Supervise and coordinate study teams to ensure smooth and compliant study execution
Regulatory & Stakeholder Management
Liaise with sponsors on medical and clinical study-related matters
Communicate with Institutional Ethics Committees (IEC) and regulatory authorities for approvals, updates, and issue resolution
Ensure all clinical activities comply with regulatory guidelines, SOPs, and Good Clinical Practice (GCP)
Safety Monitoring & Risk Management
Monitor, assess, and manage Adverse Events (AEs) and Serious Adverse Events (SAEs)
Ensure timely reporting and resolution of safety concerns in collaboration with study teams
Maintain high standards of patient safety and data integrity throughout the study lifecycle
Process Improvement & Scientific Contribution
Contribute to the scientific and operational development of the organization
Develop, review, and update departmental SOPs and clinical systems
Support continuous improvement initiatives in clinical research processes
Required Qualifications
MD in Pharmacology (mandatory)
Strong knowledge of clinical trial design, regulatory requirements, and GCP guidelines
Excellent understanding of safety reporting and pharmacovigilance processes
Strong leadership, communication, and stakeholder management skills
Experience Required
2–3 years of relevant experience in clinical research, preferably within a CRO or pharmaceutical organization
Experience in clinical trial conduct, investigator responsibilities, and protocol management
Hands-on experience in safety monitoring, AE/SAE management, and regulatory interactions
Key Skills
Clinical Trial Management
Protocol Review & Compliance
Investigator & Site Management
Safety Monitoring (AE/SAE Handling)
Regulatory & Ethics Committee Coordination
Leadership & Team Management
Scientific & Analytical Thinking
Why Join Lambda Therapeutic Research?
Work with a globally recognized full-service CRO with operations across multiple countries
Exposure to international clinical trials and diverse therapeutic areas
Collaborative and research-driven work environment
Opportunities for career advancement and professional growth
About Lambda Therapeutic Research Ltd.
Lambda Therapeutic Research is a global Contract Research Organization (CRO) headquartered in Ahmedabad, India, with a strong international presence across the USA, Canada, Europe, and Asia. The organization provides 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 advanced career opportunities in clinical research leadership.
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