Study Coordinators
2 weeks ago
We are looking for skilled Study Coordinators to join our team at ClinSync Clinical Research Pvt. Ltd., with 5-7 years of experience in the field.
Roles and Responsibility
- Coordinate and manage clinical trials, ensuring compliance with regulatory requirements and company standards.
- Develop and maintain study protocols, case report forms, and investigational reports.
- Collaborate with cross-functional teams, including data management, biostatistics, and medical writing.
- Ensure timely and accurate reporting of study progress and results.
- Manage and resolve issues related to study conduct, data quality, or patient safety.
- Maintain up-to-date knowledge of industry regulations, guidelines, and best practices.
Job Requirements
- Strong understanding of clinical trial design, methodology, and statistical analysis.
- Excellent communication, organizational, and problem-solving skills.
- Ability to work independently and as part of a team.
- Proficient in using clinical trial management systems and software applications.
- Strong attention to detail and ability to prioritize tasks effectively.
- Familiarity with Good Clinical Practice (GCP) principles and regulations.
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