Cliantha Research is a leading clinical research organization (CRO) providing end-to-end clinical trial solutions globally. Known for its expertise in biopharmaceutical and medical device research, Cliantha Research ensures high-quality data and regulatory compliance. With a strong presence in the industry, the company fosters innovation and professional growth.
Job Description
As a Clinical Team Lead, you will oversee clinical trial operations, ensuring compliance with protocols, SOPs, and regulatory guidelines.
Key Responsibilities:
✔ Lead and manage clinical monitoring teams
✔ Ensure adherence to ICH-GCP, FDA, and other regulatory guidelines
✔ Conduct site selection, initiation, monitoring, and close-out visits
✔ Review case report forms (CRFs) and source documents
✔ Train and mentor CRAs and site staff
✔ Resolve protocol deviations and data discrepancies
✔ Collaborate with sponsors, investigators, and internal teams
Skills & Competencies:
✅ Strong knowledge of clinical trial monitoring
✅ Excellent communication and leadership skills
✅ Proficiency in risk-based monitoring (RBM)
✅ Ability to handle multiple trials simultaneously
How to Apply?
Interested candidates with 8-10 years of onsite monitoring experience can send their resume to:
📧 vdesai@cliantha.com
📧 mjunnarkar@cliantha.com
Subject Line: “Application for Clinical Team Lead – [Your Name]”
