Clinical Research Coordinator
Location: Bangalore, India
Are you passionate about contributing to advancements in medical science and improving patient care? Are you detail-oriented, organized, and possess excellent communication skills? If so, we have an exciting opportunity for you to join our team as a Clinical Research Coordinator in Bangalore.
About Us:
We are a leading research organization dedicated to conducting groundbreaking clinical trials aimed at developing innovative medical treatments and therapies. Our commitment to excellence in research and patient care drives us to continually seek talented individuals to join our dynamic team.
Job Overview:
As a Clinical Research Coordinator, you will play a crucial role in the planning, coordination, and execution of clinical research studies. Working closely with investigators, sponsors, and regulatory authorities, you will ensure that all aspects of the research comply with ethical, regulatory, and protocol requirements.
Responsibilities:
- Study Coordination: Assist in the development and implementation of clinical research protocols. Coordinate study activities, including participant recruitment, informed consent procedures, and scheduling of study visits.
- Regulatory Compliance: Ensure compliance with regulatory requirements, including obtaining necessary approvals from ethics committees and regulatory authorities. Maintain accurate and up-to-date documentation throughout the research process.
- Data Management: Collect, record, and manage study data in accordance with protocol requirements and Good Clinical Practice (GCP) guidelines. Perform data quality checks and resolve discrepancies as needed.
- Participant Interaction: Serve as the primary point of contact for study participants. Provide education and support regarding study procedures, informed consent, and any potential risks or benefits associated with participation.
- Safety Monitoring: Monitor participant safety throughout the course of the study. Report adverse events and protocol deviations in a timely manner, following established procedures.
- Study Documentation: Maintain study files and documentation, including case report forms, source documents, and study-related correspondence. Ensure that all essential documents are accurate, complete, and filed appropriately.
- Collaboration: Collaborate with interdisciplinary team members, including investigators, study coordinators, clinical research associates, and data managers, to ensure the successful implementation and completion of research studies.
- Quality Assurance: Participate in internal and external quality assurance audits and inspections. Implement corrective and preventive actions as necessary to address findings and improve study processes.
Qualifications:
- Bachelor's degree in life sciences, nursing, pharmacy, or a related field.
- Previous experience in clinical research is preferred but not required for fresher candidates.
- Knowledge of regulatory requirements and guidelines governing clinical research (e.g., ICH-GCP, FDA regulations).
- Strong organizational skills and attention to detail.
- Excellent communication and interpersonal skills.
- Ability to work both independently and collaboratively in a fast-paced environment.
Additional Information:
- Age Range: We welcome candidates aged 18 to 60 years, regardless of gender.
- Location: This position is based in Bangalore, India.
- Apply Now: If you are enthusiastic about contributing to meaningful research and making a difference in healthcare, click the "Apply For Job" button below to submit your application.
Join us in our mission to advance medical knowledge and improve patient outcomes through innovative clinical research. Apply now to embark on an exciting career journey as a Clinical Research Coordinator!
