About Company IJCP GROUP www ijcpgroup com The IJCP Group was founded in 1990 by Padmashri and Dr B C Roy National Awardee Dr KK Aggarwal and was the pioneer of medical journalism in India It was started with the basic objective of updating the knowledge of the medical professionals which was the need of the day at that time and even now Job Location Marol Mumbai Near Metro Station Clinical Research Coordinator Experience Minimum 1 year Job Summary We are seeking a proactive and detail-oriented Clinical Research Coordinator CRC to support and manage clinical research activities across multiple centers The CRC will ensure adherence to protocol ICH-GCP guidelines regulatory requirements and SOPs The ideal candidate must possess a sound understanding of scientific documentation digital data systems and the ability to effectively communicate with healthcare professionals HCPs and project teams Key Responsibilities Electronic Data Capture EDC - Understand and operate EDC platforms - Fill digital forms accurately as per project-specific norms and regulatory standards Scientific Documentation CRF Management - Comprehend clinical protocols and Case Report Forms CRFs - Ensure complete and accurate CRF data entry either directly by the center or by entering data from scanned CRFs with prior approvals Center and HCP Coordination - Enroll clinical centers and HCPs in the study ensuring consent letters and necessary documentation are signed and submitted - Coordinate and dispatch study-related materials documents to participating centers Training Communication - Schedule and conduct Zoom training sessions for HCPs and site staff in collaboration with the medical team - Train sites on EDC usage study protocol and SOPs Data Quality Review - Collaborate with the medical team to review CRFs for accuracy and completeness before data lock - Ensure data queries are resolved in a timely manner Compliance SOP Adherence - Follow study-specific SOPs and regulatory guidelines GCP ICMR etc - Attend mandatory training sessions and maintain documentation of all project-related activities Documentation Logistics - Maintain organized records of courier dispatches site communications and training logs - Ensure document version control and regulatory readiness Audit Review Meetings - Be prepared and presentable to attend client audits and review meetings - Maintain updated and organized data archives to support audit-readiness and seamless review processes Qualifications Bachelor s or Master s degree in Life Sciences Pharmacy Nursing or related field Prior experience 1-3 years preferred in clinical research or site coordination Strong understanding of CRF ICH-GCP and clinical trial processes Experience working on EDC platforms is an advantage Excellent communication coordination and documentation skills Ability to multitask and work across different stakeholders with attention to detail Additional Requirements Willingness to travel if required for site visits audits or training sessions Proficiency in MS Office Zoom Teams and document tracking tools Ability to work independently and as part of a multidisciplinary team Job Types Full time Permanent Pay 15 000 00 - 32 000 00 per month Benefits Provident Fund Application Question s Current Salary Expected Salary Notice Period Looking for who can join immediate or max 30 Days Experience Clinical Research 1 year Required CRC 1 year Required Work Location In person

📌 Clinical Research Coordinator (crc) (Maharashtra)
🏢 IJCP Group
📍 Maharashtra