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 โ Clinical Research Coordinators to join their dynamic research team. If you have a Bachelorโs 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:ย Hyderabad, Telangana, India
Job Type:ย Full-time
Experience Required:ย 10+ years in clinical research
Certifications Preferred:ย 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 โ Senior Manager (Clinical Research Coordinator)
Key Responsibilities:
โย Study Coordination:ย Manage day-to-day operations ofย clinical research studies, ensuring smooth execution from initiation to completion.
โย Subject Recruitment & Enrollment:ย Oversee participant screening, ensuring compliance withย inclusion/exclusion criteria.
โย Data Collection & Management:ย Maintainย accurate, complete, and compliant study documentationย in line with regulatory standards.
โย Compliance & Protocol Adherence:ย Ensure trials followย Good Clinical Practice (GCP), ICH guidelines, and regulatory requirements.
โย Patient Care Coordination:ย Communicate with participants regardingย study visits, procedures, and follow-ups, includingย adverse event reporting.
โย Regulatory Documentation:ย Prepare and maintainย informed consent forms, case reports, ethics committee submissions, and sponsor documentation.
โย Quality Assurance:ย Conductย site audits and monitoring visitsย to ensure compliance with study protocols.
โ Training & Mentorship:ย Guide junior research staff onย clinical trial processes, GCP, and protocol adherence.
Qualifications & Skills Required
Education & Experience:
- Bachelorโs degreeย inย Life Sciences, Nursing, Pharmacy, or related field.
- Minimum 10 years of experienceย as aย Clinical Research Coordinatorย in aย hospital or clinical research setting.
- Certifications (Preferred):ย ACRP, SOCRA, or equivalent.
Essential Skills:
- Strong knowledge ofย GCP, ICH guidelines, and regulatory compliance.
- Ability toย manage multiple clinical trialsย efficiently.
- Excellentย organizational, communication, and interpersonal skills.
- Proficiency inย electronic data capture (EDC) systemsย andย clinical trial management software.
- Detail-oriented with aย strong focus on accuracy and compliance.