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Clinical Research Coordinator
Clinical Research CoordinatorConfidential • Hyderabad / Secunderabad, Telangana, India
Clinical Research Coordinator

Clinical Research Coordinator

Confidential • Hyderabad / Secunderabad, Telangana, India
26 days ago
Job description

Job Summary :

Continental Hospitals is seeking a dedicated and experienced Clinical Research Coordinator with a minimum of 3 years of experience in clinical trials . The ideal candidate will be responsible for the coordination, management, and execution of clinical research studies in compliance with applicable regulations, protocols, and institutional policies.

Key Responsibilities :

  • Study Coordination : Oversee day-to-day operations of clinical research projects, ensuring smooth and efficient execution from initiation through completion.
  • Subject Recruitment & Enrollment : Manage the recruitment and enrollment process for study participants, ensuring they meet all inclusion / exclusion criteria.
  • Data Collection & Management : Ensure accurate and timely collection of study data, 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 regarding their visits, procedures, and any 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.

Qualifications :

  • Education : Bachelor's degree in Life Sciences, Nursing, Pharmacy, or related field.
  • Experience : Minimum of 3 years of experience as a Clinical Research Coordinator or in a similar clinical research role, in Multispecialty Hospitals
  • 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.
  • Skills Required

    Regulatory Requirements

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    Clinical Coordinator • Hyderabad / Secunderabad, Telangana, India

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