✅ Lead Clinical Research as a Principal Investigator (MD Pharmacology)
Shape the Future of Medicine with Lambda Therapeutic Research
Lambda Therapeutic Research is a globally recognized, full-service Clinical Research Organization (CRO) committed to advancing healthcare through rigorous and innovative clinical trials. With our strategic footprint in Ahmedabad, Mehsana, Las Vegas, Toronto, Barcelona, London, and Warsaw, we deliver end-to-end clinical research solutions to pharmaceutical innovators worldwide.
Join us in a pivotal medical leadership role where your expertise directly influences study integrity, patient safety, and the successful development of new therapies.
Core Responsibilities & Impact
Protocol & Study Leadership
- Function as the responsible Principal Investigator or Co-Investigator for clinical studies.
- Lead the preparation, review, and finalization of study protocols and clinical study reports.
- Ensure strict compliance with approved protocols, SOPs, GCP, and regulatory requirements.
Ethics, Safety & Quality Oversight
- Coordinate and manage all activities related to the Independent Ethics Committee (IEC).
- Communicate IEC decisions, queries, and issues promptly to all stakeholders.
- Monitor, document, and manage adverse events with utmost diligence.
- Address all safety-related issues and ensure appropriate medical communication.
- Ensure timely and comprehensive responses to QA audit findings.
Strategic Collaboration & Communication
- Act as the primary medical point of contact for sponsors on study-related matters.
- Coordinate seamlessly with Project Coordinators for all project deliverables.
- Consult with specialist panels to seek expert medical opinions as required.
- Interact cross-functionally to ensure study milestones are met with scientific rigor.
Qualifications & Requirements
Essential:
- MD in Pharmacology from a recognized institution.
- Minimum 3 years of hands-on experience as a Principal Investigator or Co-Investigator in clinical research.
- In-depth knowledge of ICH-GCP, regulatory guidelines, and ethical committee processes.
- Proven experience in protocol development, study report writing, and safety management.
- Strong leadership, decision-making, and problem-solving skills.
- Excellent verbal and written communication skills in English.
Preferred:
- Experience across multiple therapeutic areas.
- Previous work in a global CRO or sponsor environment.
- Familiarity with electronic data capture (EDC) and clinical trial management systems.
Why Join Lambda Therapeutic Research?
- Global Impact: Lead studies that contribute to medical breakthroughs across continents.
- Career Growth: Clear pathway to senior medical and directorial positions within a growing global CRO.
- Expert Network: Collaborate with internationally renowned sponsors and therapeutic experts.
- Operational Excellence: Work with state-of-the-art facilities and processes in a structured, quality-driven environment.
- Diverse Portfolio: Gain exposure to a wide range of therapeutic areas and study phases.
Ready to Advance Clinical Research with Medical & Scientific Leadership?
Apply Now for the Principal Investigator Role at Lambda Therapeutic Research.
Lambda Therapeutic Research is an equal opportunity employer. We value diversity and are dedicated to creating an inclusive environment for all employees as we work together to deliver trusted clinical research outcomes globally.
