Senior Clinical Trials Data Coordinator
Behavioral Health Market Context
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Job Description
a staff
Required Qualifications
Bachelor's degree in Science, Health, or a related field, or equivalent relevant work experience
5-7 years of clinical research or related experience
Completion of Good Clinical Practice (GCP) and Human Subjects Protection (HSP) training within 1 month of employment
Ability to obtain SOCRA or ACRP certification within 2 years of employment
Experience with Clinical Trial Management Systems (CTMS) and Electronic Medical Records (EMR)
Required Qualifications
Bachelor's degree in Science, Health, or a related field, or equivalent relevant work experience
5-7 years of clinical research or related experience
Completion of Good Clinical Practice (GCP) and Human Subjects Protection (HSP) training within 1 month of employment
Ability to obtain SOCRA or ACRP certification within 2 years of employment
Experience with Clinical Trial Management Systems (CTMS) and Electronic Medical Records (EMR)
Qualifications
- •Bachelor's degree in Science, Health, or a related field, or equivalent relevant work experience
- •5-7 years of clinical research or related experience
- •Completion of Good Clinical Practice (GCP) and Human Subjects Protection (HSP) training within 1 month of employment
- •Ability to obtain SOCRA or ACRP certification within 2 years of employment
- •Experience with Clinical Trial Management Systems (CTMS) and Electronic Medical Records (EMR)
Benefits
Responsibilities
- •Coordinate data collection, entry, quality assurance, and query resolution for oncology clinical trials
- •Ensure data accuracy and compliance with regulatory guidelines while managing adverse event documentation
- •Support monitoring visits and contribute to data management improvements and training of research data staff
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