Company Description
C-TrialPro is a premier Site Management Organization (SMO) dedicated to providing high-quality clinical trial management services for pharmaceutical, biotechnology, and medical device companies. Our mission is to support the development of groundbreaking treatments through efficient and cost-effective clinical trial solutions. With expertise in site management, patient recruitment, data management, and regulatory affairs, we ensure seamless trial operations. Our commitment to quality assurance and compliance helps deliver reliable results and supports innovation in healthcare.
Role Description
This is a full-time, on-site role located in Kolkata for a Clinical Research Coordinator. The Clinical Research Coordinator will oversee and manage clinical trial activities, ensuring that protocols are followed and regulatory requirements are met. Responsibilities include conducting informed consent, coordinating with research teams, monitoring clinical trial processes, and maintaining accurate documentation. The role also involves managing patient recruitment and retention efforts, along with ensuring adherence to compliance and ethical standards.
Qualifications
- Proficiency with Informed Consent procedures and processes
- Familiarity with clinical trial Protocol implementation and adherence
- Experience with Research and Clinical Research operations
- Understanding and hands-on experience with Clinical Trials
- Strong organizational and documentation skills
- Excellent interpersonal and communication abilities for effective collaboration
- Bachelor's degree in life sciences, healthcare, or a related field
- Certification as a Clinical Research Professional (preferred)
- Knowledge of regulatory guidelines and good clinical practice (GCP) standards
