We are seeking dedicated and enthusiastic individuals to join our team as Clinical Research Coordinators. At Catalyst, we are committed to advancing clinical research and improving patient outcomes through innovative and rigorous clinical trials.
Vacancy Details :
- Position Name : Clinical Research Coordinator (3 Positions)
- Organization : Catalyst Clinical Services Pvt Ltd
- Qualification: B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences
- Experience: 0 YEARS / Freshers – 1 Year
- Salary: 25,000 – 35,000 /month
- Location: Delhi
Description :
Study Coordination and Management:
- Coordinated and managed all aspects of clinical trials, including recruitment, screening, and enrollment of study participants.
- Maintained accurate and up-to-date study documentation, including informed consent forms, case report forms, and regulatory binders.
Regulatory Compliance:
- Ensured compliance with Good Clinical Practice (GCP), Institutional Review Board (IRB) requirements, and all applicable regulations and guidelines.
- Prepared and submitted regulatory documents to IRBs and other oversight bodies, ensuring timely approvals and renewals.
Patient Interaction and Support:
- Conducted informed consent discussions, educating participants about the study purpose, procedures, and potential risks and benefits.
- Monitored participant safety and well-being throughout the study, managing adverse events and providing necessary support and follow-up care.
Data Collection and Management:
- Collected, recorded, and managed clinical trial data accurately and efficiently, ensuring data integrity and quality.
- Utilized electronic data capture (EDC) systems and other data management tools to streamline data entry and tracking processes.
Study Implementation and Monitoring:
- Implemented study protocols and procedures, ensuring adherence to study timelines and objectives.
- Conducted regular monitoring visits and audits to assess study progress, identify issues, and implement corrective actions.
Collaboration and Communication:
- Collaborated with principal investigators, study sponsors, and other stakeholders to facilitate study operations and address challenges.
- Communicated study updates, findings, and requirements to research teams, ensuring alignment and informed decision-making.
Training and Education:
- Trained and supervised research staff and students on study protocols, regulatory requirements, and data management practices.
- Developed and delivered educational materials and sessions for participants and staff to enhance study comprehension and compliance.
Quality Assurance and Improvement:
- Implemented quality assurance processes to monitor and improve study conduct and data quality.
- Identified opportunities for process improvements and implemented strategies to enhance study efficiency and effectiveness.
How to Apply :
Interested candidates are invited to send their CV to Pulkit at- pulkit@catalystclinicalservices.com.