Job Title: Manager
Company: Lambda Therapeutic Research Ltd.
Location: Ahmedabad, India
Job ID: 1468
Employment Type: Full-Time
CTC Range: INR 8,00,000 – 15,00,000 per annum
Experience Required: 2–3 years
About the Company
Lambda Therapeutic Research Ltd. is a globally recognized full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India. The organization operates advanced clinical research facilities in Mehsana (India), Las Vegas (USA), Toronto (Canada), Barcelona (Spain), London (UK), and Warsaw (Poland).
Lambda provides comprehensive end-to-end clinical research solutions to global pharmaceutical, biotechnology, and generic drug companies. With a strong focus on scientific excellence, regulatory compliance, and operational efficiency, the organization supports innovative drug development programs across multiple therapeutic areas.
Job Overview
Lambda Therapeutic Research Ltd. is seeking a qualified Manager to support clinical research operations and medical oversight of clinical studies. The role involves functioning as a Study Physician or Co-Investigator responsible for clinical assessments, volunteer screening, protocol compliance, and safety management in clinical trials.
The selected candidate will collaborate with cross-functional teams, including project coordinators, ethics committees, sponsors, and regulatory teams, to ensure high-quality study execution while maintaining compliance with Good Clinical Practice (GCP), regulatory standards, and organizational SOPs.
Key Responsibilities
Act as a Co-Investigator or Study Physician for clinical research studies conducted at the facility.
Perform medical screening and clinical evaluation of volunteers to determine eligibility for participation in clinical trials.
Support volunteer recruitment and screening activities in coordination with the screening and recruitment teams.
Conduct clinical examinations and ensure accurate medical assessments of study participants.
Monitor adverse events and coordinate follow-up activities with volunteer management teams.
Prepare, review, and support the development of clinical study protocols.
Coordinate with Institutional Ethics Committees (IEC) and communicate study-related updates to relevant stakeholders.
Ensure strict adherence to study protocols, standard operating procedures (SOPs), and regulatory guidelines.
Collaborate with project coordinators on study planning, implementation, and execution activities.
Monitor safety data and manage adverse events while ensuring timely responses to quality assurance observations.
Interact with study sponsors regarding medical and safety-related aspects of clinical trials.
Manage safety-related issues and ensure appropriate documentation and communication.
Prepare and review clinical study reports and medical documentation.
Maintain confidentiality of medical records and ensure accurate case management.
Support the development, maintenance, and updating of departmental systems and SOPs.
Perform additional responsibilities as assigned by department leadership or management.
Technical Skills
Strong knowledge of clinical trial processes and regulatory requirements.
Familiarity with Good Clinical Practice (GCP) guidelines and ethical standards in clinical research.
Experience in clinical examination, adverse event management, and protocol compliance.
Understanding of clinical documentation, reporting, and medical case management.
Soft Skills
Strong communication and interpersonal skills.
Ability to collaborate with cross-functional teams and external stakeholders.
High level of attention to detail and patient safety.
Strong organizational and problem-solving abilities.
Educational Qualification
MBBS (Bachelor of Medicine, Bachelor of Surgery).
Job Category: Clinical Research / Medical Affairs / Study Physician
How to Apply
Interested candidates with relevant clinical research experience are encouraged to apply through the official careers portal of Lambda Therapeutic Research Ltd. or explore additional pharmaceutical and clinical research opportunities on ThePharmaDaily.com.
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