Clinical Research Coordinator Jobs at Continental Hospitals Hyderabad

Clinical Research Coordinator Recruitment at Continental Hospitals Hyderabad: Join a Leader in Healthcare Innovation

Continental Hospitals, a premier healthcare institution in Hyderabad, seeks experienced Clinical Research Coordinators to join its dynamic research team. Suppose you have a Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or a related field and minimum of 10 years in clinical trials. In that case, this is your opportunity to contribute to cutting-edge medical research in a world-class hospital setting.

About Continental Hospitals
Continental Hospitals is a leading multi-speciality healthcare provider in Hyderabad. It is known for its state-of-the-art infrastructure and commitment to excellence in patient care and medical research. The hospital is dedicated to advancing healthcare through innovative clinical trials and research studies, ensuring better patient outcomes worldwide.

Job Overview

• Position: Sr Manager – Clinical Research Coordinator
• Location: Hyderabad, Telangana, India
• Experience Required: Minimum of 10 years
• QuBachelor’snss:Bachelor’ss degree in Life Sciences, Nursing, Pharmacy, or a related field
• Certifications: ACRP or SOCRA certification is preferred

Job Summary:

Continental Hospitals is seeking a dedicated and experienced Clinical Research Coordinator with a minimum of 4 years of experience in clinical trials to join our dynamic research team. The ideal candidate will be responsible for coordinating, managing, and executing clinical research studies in compliance with applicable regulations, protocols, and institutional policies.

Key Responsibilities:

• Study Coordination: I oversee the day-to-day operations of clinical research projects, ensuring smooth and efficient execution from initiation through completion.
• Subject Recruitment & Enrollment:Participants” recruitment and enrollment process, ensuring they meet all inclusion/exclusion criteria.
• Data Collection & Management: Ensure accurate and timely study data collection and maintain complete, organized, and compliant study documentation.
• Compliance & Protocol Adherence: Ensure all clinical trials are conducted according to Good Clinical Practice (GCP), ICH guidelines, and regulatory requirements. Monitor adherence to the study protocol and make necessary adjustments as needed.
• Patient Care Coordination: Communicate with study participants about their visits, procedures, and other relevant study information. Ensure proper follow-up, including adverse event reporting and participant safety.
• Collaborative Coordination: Liaise with internal and external stakeholders, including research teams, physicians, and regulatory bodies, to facilitate the successful completion of clinical trials.
• Regulatory Documentation: Prepare and maintain all regulatory documentation, including informed consent forms, case report forms, ethics committee submissions, and sponsor-related documentation.
• Quality Assurance: Conduct routine site visits and audits, ensuring compliance with all study-related activities and providing corrective actions where necessary.
• Training & Mentorship: Train and mentor junior research staff and new hires in clinical trial processes, protocols, and GCP standards.

QualificationBachelor’s

• : Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or related field.
• Experience: minimum of 10 years EXPERIENCE  as a Clinical Research Coordinator or in a similar clinical research role, preferably in a hospital or clinical setting.
• Certifications: Certification in Clinical Research (e.g., ACRP or SOCRA) is preferred.
• Skills:
• Strong knowledge of GCP, ICH guidelines, and regulatory requirements.
• Ability to manage multiple clinical trials simultaneously.
• Excellent organizational and time management skills.
• Strong interpersonal and communication skills, both written and verbal.
• Detail-oriented with a focus on accuracy and compliance.
• Ability to work collaboratively in a team environment and independently as needed.

Preferred Qualifications:

• Experience with electronic data capture (EDC) systems and clinical trial management software.
• Experience with hospital-based clinical research trials, patient recruitment, and compliance monitoring.

How to Apply
If you meet the qualifications and are passionate about clinical research, apply now for the Clinical Research Coordinator position at Continental Hospitals Hyderabad. Submit your application via LinkedIn: Apply Now.

Tagged as: Global Pharma Jobs, Good Clinical Practice (GCP), Pharmaceutical Careers, Pharmaceutical Jobs