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Life Sciences CRC Jobs at Canvass Clinical Research Services, Apply on Biotecnika
Looking for rewarding Life Sciences CRC Jobs at Canvass Clinical Research Services? Apply on Biotecnika to explore exciting career opportunities in clinical research and data management. Join a leading organization where you can contribute to innovative life sciences projects, gain hands-on experience, and advance your career in the pharmaceutical and clinical research industry. Don’t miss your chance to be part of Canvass Clinical Research Services’ dynamic team.
Job Title: Clinical Research Coordinator
Company Name: Canvass Clinical Research Services Pvt. Ltd
Experience: 6 month – 1year experience
CTC: ₹2.4 L – ₹3 LPA Or Hike on last withdrawn CTC
Number of vacancies: above 1
Rounds of interview: 2 rounds Virtual
Qualification: B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences
Location: Nagpur
Job Summary:
The Clinical Research Coordinator at Canvass Clinical Research Services Pvt. Ltd.
plays a critical role in the successful execution of clinical trials at the site level.
This role involves coordinating clinical trial operations, managing study
participants, maintaining high-quality data, and ensuring adherence to GCP and
regulatory standards. Based in Nagpur, this full-time position is ideal for
professionals with at least one year of CRC experience who are seeking hands-
on exposure to clinical trials, strong learning opportunities, and long-term career growth
in the clinical research industry.
Responsibilities:
• Coordinate day-to-day clinical trial activities at the site, including scheduling, resource
allocation, and workflow management to ensure timely study progress.
• Manage subject recruitment, screening, enrollment, and follow-up visits to ensure
participant retention and adherence to study timelines.
• Maintain accurate and complete trial documentation and source records, including
CRFs, informed consent forms (ICFs), and source data.
• Perform data entry, verification, and updates in Electronic Data Capture (EDC) systems
(e.g., Medidata Rave or similar), and resolve data queries or discrepancies.
• Ensure strict compliance with study protocols, ICH-GCP guidelines, and applicable
regulatory requirements (including CDSCO), and support audit readiness.
• Support Principal Investigators (PIs), sub-investigators, and the clinical research team
by coordinating communication, addressing queries, and providing study updates.
• Assist during monitoring visits, audits, and inspections by preparing site documents,
accompanying CRO monitors, and implementing corrective actions as required.
• Track study timelines, milestones, and deliverables to ensure timely completion of trial
activities and reporting.
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