LEADS CLINICAL RESEARCH AND BIO SERVICES PVT LTDS

3 Job openings at LEADS CLINICAL RESEARCH AND BIO SERVICES PVT LTDS
Senior Clinical Research Coordinator bengaluru 3 years INR 3.0 - 4.8 Lacs P.A. On-site Full Time

Leads Clinical Research and Bio Services Pvt. Ltd is hiring Clinical Research Coordinators in Chennai and Bangalore. Experience: 3 years months to 6 years Qualification: Degree with Life Science background, Diploma in Clinical Research, MSc. Clinical Research, Pharm D Core Responsibilities Coordinate Screening and Consenting process, Source documentation Update Site Master Files and EDC data entries and query resolutions Investigational product accountability and maintain logs Ethics committee related documentation Job Type: Full-time Pay: ₹25,000.00 - ₹40,000.00 per month Work Location: In person

Clinical Research Coordinator chennai, tamil nadu 1 years INR 1.8 - 3.0 Lacs P.A. On-site Full Time

Leads Clinical Research and Bio Services Pvt. Ltd is hiring Clinical Research Coordinators in Chennai and Bangalore. Experience: 1 year months to 3years Qualification: Degree with Life Science background, Diploma in Clinical Research, MSc. Clinical Research, Pharm D Core Responsibilities Coordinate Screening and Consenting process, Source documentation Update Site Master Files and EDC data entries and query resolutions Investigational product accountability and maintain logs Ethics committee related documentation Job Type: Full-time Pay: ₹15,000.00 - ₹25,000.00 per month Experience: total work: 1 year (Preferred) Work Location: In person

Clinical Research Coordinator chennai,tamil nadu 1 - 5 years INR Not disclosed On-site Full Time

You will be responsible for coordinating various aspects of clinical research activities at Leads Clinical Research and Bio Services Pvt. Ltd in Chennai and Bangalore. Your key responsibilities will include: - Coordinating the screening and consenting process, as well as maintaining source documentation - Updating Site Master Files, EDC data entries, and resolving queries - Ensuring investigational product accountability and maintaining related logs - Handling ethics committee documentation You should have a minimum of 1 year of total work experience and a qualification that includes a degree with a background in Life Science, Diploma in Clinical Research, MSc. Clinical Research, or Pharm D. This is a full-time job that requires in-person work at the specified locations.,