Clinical Research Associate

Role Overview: You will be assisting in the preparation and coordination of clinical trial protocols and associated documents. Your responsibilities will include supporting the monitoring of clinical trials at various stages, ensuring compliance with Good Clinical Practice (GCP) and regulatory requirements, conducting site visits, and communicating with investigators and site staff. Key Responsibilities: - Assist in the preparation and coordination of clinical trial protocols and associated documents - Support the monitoring of clinical trials at various stages - Ensure study sites are compliant with Good Clinical Practice (GCP) and regulatory requirements - Conduct site visits to assess trial progress, monitor data accuracy, and ensure patient safety - Communicate with investigators and site staff to address issues or concerns - Review and manage clinical trial documentation including case report forms (CRFs) and informed consent forms - Maintain study files and data to ensure compliance with regulatory agencies - Support the clinical team in preparing reports and regulatory documents - Attend internal meetings and training sessions to enhance knowledge and skills in clinical research Qualifications Required: - Bachelor's degree in a related field (e.g., life sciences, healthcare) - Understanding of Good Clinical Practice (GCP) guidelines - Strong attention to detail and organizational skills - Excellent communication and interpersonal skills - Ability to work effectively in a team environment Please note that this job is full-time and suitable for freshers. Kindly note that the work location for this role is in person. Benefits include health insurance, paid sick time, and provident fund. Role Overview: You will be assisting in the preparation and coordination of clinical trial protocols and associated documents. Your responsibilities will include supporting the monitoring of clinical trials at various stages, ensuring compliance with Good Clinical Practice (GCP) and regulatory requirements, conducting site visits, and communicating with investigators and site staff. Key Responsibilities: - Assist in the preparation and coordination of clinical trial protocols and associated documents - Support the monitoring of clinical trials at various stages - Ensure study sites are compliant with Good Clinical Practice (GCP) and regulatory requirements - Conduct site visits to assess trial progress, monitor data accuracy, and ensure patient safety - Communicate with investigators and site staff to address issues or concerns - Review and manage clinical trial documentation including case report forms (CRFs) and informed consent forms - Maintain study files and data to ensure compliance with regulatory agencies - Support the clinical team in preparing reports and regulatory documents - Attend internal meetings and training sessions to enhance knowledge and skills in clinical research Qualifications Required: - Bachelor's degree in a related field (e.g., life sciences, healthcare) - Understanding of Good Clinical Practice (GCP) guidelines - Strong attention to detail and organizational skills - Excellent communication and interpersonal skills - Ability to work effectively in a team environment Please note that this job is full-time and suitable for freshers. Kindly note that the work location for this role is in person. Benefits include health insurance, paid sick time, and provident fund.