Key Responsibilities:

Manage and maintain the data collection process for clinical trials, including tracking of study progress and data entry.
Perform quality checks on clinical trial data to ensure accuracy and completeness.
Develop and maintain data management plans and study-specific documentation.
Collaborate with study team members to identify and resolve data discrepancies.
Assist with database development and participate in user acceptance testing.
Generate data reports and provide regular updates to the clinical research team.
Ensure compliance with all relevant regulations and guidelines for data management and clinical research.
Maintain a thorough understanding of study protocols, data collection procedures, and study timelines.
Participate in study meetings and provide updates on data management activities.
Assist with data coding and data cleaning processes as needed.
Provide support for audits and inspections related to data management activities.

Qualifications:

Bachelor��s degree in a scientific or healthcare-related field.
Minimum of 2 years of experience in clinical data management.
Strong understanding of clinical research processes and regulations.
Proficient in data management systems and tools, such as EDC systems and Microsoft Excel.
Excellent attention to detail and organizational skills.
Ability to work independently and as part of a team.
Strong communication and interpersonal skills.
Experience with coding medical terminology is a plus.

This is an exciting opportunity to join a growing company and make a meaningful impact in the field of clinical research. If you are a self-motivated and detail-oriented individual looking for a challenging and rewarding position, we encourage you to apply for the role of Clinical Data Coordinator.

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