Clinical Trial Assistant
1 week ago
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.
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