Are you an experienced Clinical Research Coordinator looking for a rewarding career in Hyderabad? Continental Hospitals, a leading multi-specialty healthcare provider, is hiring Senior Managers – Clinical Research Coordinators to join their dynamic research team. If you have a Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or a related field and a minimum of 10 years of experience in clinical trials, this could be your ideal opportunity.
Location: Hyderabad, Telangana, India
Job Type: Full-time
Experience Required: 10+ years in clinical research
Certifications Preferred: ACRP or SOCRA
About Continental Hospitals
Continental Hospitals is a premier healthcare institution in Hyderabad, known for its state-of-the-art infrastructure, advanced medical research, and patient-centric care. The hospital is committed to innovative clinical trials that contribute to global healthcare advancements. By joining their team, you will be part of a world-class research environment that fosters professional growth and excellence.
Job Overview – Senior Manager (Clinical Research Coordinator)
Key Responsibilities:
✔ Study Coordination: Manage day-to-day operations of clinical research studies, ensuring smooth execution from initiation to completion.
✔ Subject Recruitment & Enrollment: Oversee participant screening, ensuring compliance with inclusion/exclusion criteria.
✔ Data Collection & Management: Maintain accurate, complete, and compliant study documentation in line with regulatory standards.
✔ Compliance & Protocol Adherence: Ensure trials follow Good Clinical Practice (GCP), ICH guidelines, and regulatory requirements.
✔ Patient Care Coordination: Communicate with participants regarding study visits, procedures, and follow-ups, including adverse event reporting.
✔ Regulatory Documentation: Prepare and maintain informed consent forms, case reports, ethics committee submissions, and sponsor documentation.
✔ Quality Assurance: Conduct site audits and monitoring visits to ensure compliance with study protocols.
✔ Training & Mentorship: Guide junior research staff on clinical trial processes, GCP, and protocol adherence.
Qualifications & Skills Required
Education & Experience:
- Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or related field.
- Minimum 10 years of experience as a Clinical Research Coordinator in a hospital or clinical research setting.
- Certifications (Preferred): ACRP, SOCRA, or equivalent.
Essential Skills:
- Strong knowledge of GCP, ICH guidelines, and regulatory compliance.
- Ability to manage multiple clinical trials efficiently.
- Excellent organizational, communication, and interpersonal skills.
- Proficiency in electronic data capture (EDC) systems and clinical trial management software.
- Detail-oriented with a strong focus on accuracy and compliance.
