Clinical Data Coordinator (Boston, MA; Dallas, TX; ...)

Job Overview:
We are seeking a Clinical Data Coordinator on a contract basis to support our clinical data management team. In this role, you will be responsible for the accurate collection, entry, and maintenance of clinical trial data, ensuring it meets quality standards and regulatory requirements.

Key Responsibilities:

Data Collection & Entry

• Support the collection, review, and entry of clinical trial data into electronic data capture (EDC) systems.
• Monitor data for completeness, consistency, and accuracy to maintain data integrity.

Data Quality & Compliance

• Perform data validation checks and resolve data discrepancies in collaboration with clinical sites and study teams.
• Ensure data is collected in compliance with Good Clinical Practice (GCP), study protocols, and company SOPs.

Documentation & Reporting

• Assist in the preparation and maintenance of data management documentation, including data review guidelines, data entry manuals, and query resolution logs.
• Generate data reports and summaries as required for study teams and project managers.

Collaboration & Support

• Work closely with clinical research associates, data managers, and other cross-functional team members to facilitate smooth data management processes.
• Participate in data review meetings and contribute to problem-solving for data issues as needed.

Qualifications:

• Bachelor's degree in life sciences, health sciences, or a related field.
• 1-3 years of experience in clinical data management or clinical research is preferred.
• Familiarity with EDC systems, data entry, and basic data management principles.
• Strong organizational skills and keen attention to detail.
• Excellent communication skills and ability to work both independently and as part of a team.

This is a contract position