Clinical Trial Assistant

We are seeking a highly organized and detail-oriented Clinical Trial Coordinator (Fresher) to join our dynamic clinical research team. In this role, you will play a crucial part in ensuring the successful execution of our clinical trials from start to finish. You will collaborate with a multidisciplinary team of researchers, investigators, and study personnel to coordinate all aspects of clinical trial operations.

Key Responsibilities:

• Study Coordination:

  Coordinate the day-to-day activities of assigned clinical trials, ensuring adherence to protocols, timelines, and regulatory requirements.

• Site Management:

  Assist in site selection, initiation, monitoring, and close-out activities.

• Documentation:

  Maintain accurate and complete study records, including case report forms, source documents, and regulatory binders.

• Communication:

  Facilitate effective communication between study sites, sponsors, investigators, and internal team members.

• Data Management:

  Ensure timely and accurate data collection, entry, and query resolution.

• Regulatory Compliance:

  Ensure compliance with all applicable regulations, guidelines, and standard operating procedures.

• Patient Recruitment:

  Support patient recruitment and retention efforts.

• Training:

  Provide training and support to study staff on study protocols and procedures.

• Quality Assurance:

  Participate in quality control activities and internal audits.

Qualifications and Skills:

• Education:

  Bachelor's degree in life sciences, nursing, or a related field.

• Experience:

  Fresher or recent graduate with a strong interest in clinical research.

• Knowledge:

  Basic understanding of clinical research principles and Good Clinical Practice (GCP).

• Skills:

  Excellent organizational, communication, and interpersonal skills.