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Clinical Research Coordinator Job | Continental Hospitals Careers
Continental Hospitals is inviting applications for the position of Clinical Research Coordinator. If you’re passionate about advancing medical science and managing clinical trials with precision, this is your opportunity to grow your career with one of India’s most respected healthcare institutions. This Clinical Research Coordinator job is ideal for professionals with over 3 years of experience seeking to make a real impact in life science jobs in Hyderabad and contribute to cutting-edge research through Continental Hospitals careers.
Job Details:
- Job Position: Clinical Research Coordinator
- Location: Continental Hospitals, Hyderabad, India
About the Company:
Continental Hospitals is a premier multispecialty healthcare provider in Hyderabad, known for its excellence in clinical care, innovation, and medical research. As part of Continental Hospitals careers, professionals gain access to advanced infrastructure, world-class research facilities, and opportunities to contribute to life-changing discoveries. The institution is dedicated to fostering growth and excellence among individuals pursuing life science jobs in Hyderabad.
Qualifications:
- Education: Bachelor’s degree in Life Sciences or related field.
- Experience: Minimum of 3 years as a Clinical Research Coordinator or in a related clinical research role at multispecialty hospitals.
- Certifications: Preferred certification in Clinical Research (ACRP or SOCRA).
Clinical Research Coordinator Job Description:
The Clinical Research Coordinator will manage and coordinate clinical research studies while ensuring compliance with regulatory standards, institutional policies, and study protocols. This role is vital for the success of Continental Hospitals’ clinical research programs, where you’ll support the development of new therapies and innovative patient care.
Key Responsibilities:
- Study Coordination: Manage daily operations of clinical research projects from initiation through completion.
- Subject Recruitment & Enrollment: Recruit eligible participants and ensure all inclusion and exclusion criteria are met.
- Data Collection & Management: Maintain accurate, organized, and compliant study data.
- Compliance & Protocol Adherence: Follow GCP, ICH guidelines, and study protocols to ensure trial integrity.
- Patient Care Coordination: Communicate with participants and ensure their safety throughout the study.
- Collaborative Coordination: Work with investigators, internal research teams, and regulatory bodies for smooth execution.
- Regulatory Documentation: Prepare informed consent forms, ethics committee submissions, and sponsor documents.
- Quality Assurance: Conduct site visits, perform audits, and implement corrective actions when needed.
- Training & Mentorship: Support and mentor junior research staff on trial processes and GCP standards.
Clinical Research Coordinator Job – Skills:
- Strong understanding of GCP, ICH, and regulatory requirements.
- Excellent communication, organization, and time management abilities.
- Proficiency with clinical trial management software and electronic data capture (EDC) systems.
- Ability to handle multiple studies simultaneously and ensure data accuracy.
- Collaborative mindset and attention to compliance standards.
