Job Title: Manager – Clinical Research (Principal Investigator)
Req ID: 1147
Location: Ahmedabad, Gujarat, India
Company: Lambda Therapeutic Research Ltd.
CTC Range: INR 16,00,000 – 20,00,000 per annum
Experience Required: Minimum 3 years of relevant clinical research experience
Job Type: Full-Time | On-Site | Permanent
Job Category: Clinical Research | Medical Affairs | Pharmacology | CRO Operations
About the Company
Lambda Therapeutic Research Ltd. is a global full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India. With strategically located facilities in Mehsana (India), Las Vegas (USA), Toronto (Canada), Barcelona (Spain), London (UK), and Warsaw (Poland), the organization provides comprehensive end-to-end clinical research services to innovators, biotechnology companies, and generic pharmaceutical firms worldwide.
The company supports Phase I–IV clinical trials with strong expertise in regulatory compliance, medical oversight, pharmacovigilance, and global clinical operations.
Role Overview
The Manager – Clinical Research will function as a Principal Investigator (PI) or Co-Investigator (Co-I), providing medical and scientific leadership for clinical studies. The role requires in-depth knowledge of clinical trial conduct, regulatory compliance, pharmacovigilance, and ethical oversight.
This position plays a critical role in ensuring protocol adherence, subject safety, sponsor communication, and inspection readiness within a regulated CRO environment.
Key Responsibilities
Function as Principal Investigator or Co-Investigator for assigned clinical studies
Prepare, review, and provide medical input on clinical study protocols
Coordinate activities related to Institutional Ethics Committee (IEC) submissions and approvals
Communicate IEC-related updates and requirements to internal stakeholders
Ensure compliance with study protocols, SOPs, ICH-GCP guidelines, and regulatory requirements
Collaborate with Project Coordinators on all project-related operational matters
Monitor, assess, and manage adverse events and serious adverse events
Coordinate with medical consultants to obtain expert opinions when required
Ensure timely and appropriate responses to Quality Assurance (QA) findings
Interact with sponsors on medical and safety-related matters
Oversee safety reporting and ensure appropriate communication to regulatory authorities
Prepare and review clinical study reports and related documentation
Required Experience
Minimum 3 years of experience in clinical research
Experience functioning as Principal Investigator or Sub-Investigator preferred
Strong understanding of ICH-GCP guidelines, regulatory frameworks, and IEC processes
Hands-on experience in adverse event management and safety reporting
Strong medical writing, sponsor communication, and compliance management skills
Educational Qualifications
MD in Pharmacology (Mandatory)
Uttar Pradesh :
Agra | Gajraula | Gautam buddha Nagar | Ghaziabad | Gorakhpur | Greater Noida | Jhansi | kanpur | Lucknow | Mathura | Noida | Park City | Prayagraj | Satyamev | Varanasi |Gujarat :
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Siliguri |Illinois :
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Bulgaria | Vedant |Denmark :
Copenhagen | Denmark |Europe :
Europe | France | Latvia | Lendava | Leuven | Poland | Slovenia | Spain |Finland :
Finland |Istanbul :
Istanbul | Turkey |Norway :
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Netherlands |Remote Australia :
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England | Harlow | Leeds | London | Maidenhead | Salt Lake City | Stevenage | Stirling | United Kingdom |North Yorkshire :
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Sheffield |Oxfordshire :
Witney |Ontario :
Renfrew | Uxbridge | Australia | Richmond Hill | Mississauga | North York |Canada :
Canada |Quebec :
Montreal |Brussels :
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Heist op den Berg |Flemish Brabant :
Zaventem |South America :
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Sao paulo | Brazil |Attica :
Koropi | Athens |Greece :
Greece |North Island :
Auckland |New Zealand :
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Manila |Croatia :
Croatia |Zagreb :
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Tallinn |Hà Nội :
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Oulu |Southwest Finland (Varsinais-Suomi) :
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Remote Korea |Republic of Korea :
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