Are you an MD in Pharmacology looking for a dynamic leadership role in clinical research? Lambda Research Accelerated, operating under Novum Pharmaceutical Research Services, is actively seeking a dedicated and experienced Principal Investigator to join our esteemed team in Ahmedabad. This is a fantastic opportunity to advance your career with a global Contract Research Organization (CRO) at the forefront of pharmaceutical innovation.
About Lambda Research / Novum Pharmaceutical Research Services
Lambda Research is a prominent global Contract Research Organization (CRO) providing comprehensive clinical trial services to the pharmaceutical and biotechnology industries. With a strong operational presence across India, the USA, Canada, the UK, Spain, and Poland, we are committed to accelerating the development of new therapies through scientific excellence and rigorous research standards.
Our parent platform, Novum Pharmaceutical Research Services (www.novumprs.com), is a well-known name in the industry, and we also run Pharmabharat.org, a dedicated platform for the pharma community in India. Working with us means being part of a culturally diverse and scientifically stimulating environment where your work makes a real impact on global health.
Job Description: Principal Investigator
Location: Ahmedabad, India
Required Qualification: MD (Pharmacology) with 2-3 years of relevant experience in clinical research.
As a Principal Investigator at Lambda Research, you will be the cornerstone of our clinical trials, responsible for the scientific and ethical integrity of the study at the site. You will play a critical role in leading our research efforts and ensuring the highest standards of patient safety and data quality.
Key Responsibilities:
- Conduct in-depth feasibility assessments of potential molecules and provide expert reviews of clinical study protocols sponsored by our clients.
- Act as the Principal Investigator for assigned studies, taking ultimate responsibility for the conduct of the trial at the site.
- Perform thorough eligibility screenings and continuous compliance checks to ensure all participants strictly adhere to the study protocol.
- Provide coordination, leadership, and supervision to the entire study team, ensuring compliance with the protocol, Standard Operating Procedures (SOPs), and all relevant regulatory guidelines (ICMR GCP, FDA, etc.).
- Serve as the primary point of contact for sponsors on all medical and scientific matters related to the study.
- Liaise with the Independent Ethics Committee (IEC) and other regulatory authorities, providing them with necessary study updates and promptly addressing any concerns.
- Take charge of safety management, including the coordination, monitoring, and reporting of Adverse Events (AEs) and Serious Adverse Events (SAEs).
- Contribute to the organization’s scientific growth by helping to maintain, update, and develop departmental systems and SOPs.
How to Apply
If you are an MD in Pharmacology with a passion for clinical research and meet the experience requirements, we encourage you to apply!
Please email your updated CV or profile to:
saurabhkharya@lambda-cro.com
