Entry Level Document Control / Project Support Coordinator | Clinical Research
18–21 an hour
Behavioral Health Market Context
Apply Nowvia Glassdoor
Benefits
Health InsuranceDental CoveragePaid Time Off
Job Description
l advancements. This paid position offers an exciting opportunity to develop your skills in clinical trials management while making a meaningful impact on patient care and scientific discovery.
Duties
• Assist in the collection, review, and organization of source documents for clinical trials, ensuring completeness and adherence to protocol specifications.
• Support the creation and maintenance of source document builder templates aligned with GCP-ICH standards and regulatory requirements.
• Review clinical trial documentation for consistency, accuracy, and regulatory compliance before submission or archiving.
• Contribute to data management efforts by organizing source documents for efficient retrieval and audit readiness.
Qualifications
• Demonstrated ability to coordinate multiple tasks within a clinical research environment.
• Able to communicate fluently in English and Spanish
• Knowledge of basic clinical trials management, including familiarity with FDA regulations, ICH GCP standards, and CDISC data standards.
• Strong understanding of medical terminology, clinical laboratory procedures, blood sampling techniques, and patient monitoring protocols.
• Experience reviewing documentation for accuracy, completeness, and compliance with regulatory standards such as HIPAA and GCP.
• Proficiency in statistical software tools used for data analysis within clinical research settings.
• Background in clinical development or nursing with hands-on experience in clinical trials or laboratory environments preferred.
• Excellent organizational skills with attention to detail; ability to adhere strictly to compliance management protocols. Embark on a rewarding journey where your expertise fuels innovative healthcare solutions! We are committed to fostering an inclusive environment that supports your professional growth while contributing to life-changing medical research.
Pay: $18.00 - $21.00 per hour
Benefits:
• Dental insurance
• Health insurance
• Paid time off
• Vision insurance
Work Location: In person
Duties
• Assist in the collection, review, and organization of source documents for clinical trials, ensuring completeness and adherence to protocol specifications.
• Support the creation and maintenance of source document builder templates aligned with GCP-ICH standards and regulatory requirements.
• Review clinical trial documentation for consistency, accuracy, and regulatory compliance before submission or archiving.
• Contribute to data management efforts by organizing source documents for efficient retrieval and audit readiness.
Qualifications
• Demonstrated ability to coordinate multiple tasks within a clinical research environment.
• Able to communicate fluently in English and Spanish
• Knowledge of basic clinical trials management, including familiarity with FDA regulations, ICH GCP standards, and CDISC data standards.
• Strong understanding of medical terminology, clinical laboratory procedures, blood sampling techniques, and patient monitoring protocols.
• Experience reviewing documentation for accuracy, completeness, and compliance with regulatory standards such as HIPAA and GCP.
• Proficiency in statistical software tools used for data analysis within clinical research settings.
• Background in clinical development or nursing with hands-on experience in clinical trials or laboratory environments preferred.
• Excellent organizational skills with attention to detail; ability to adhere strictly to compliance management protocols. Embark on a rewarding journey where your expertise fuels innovative healthcare solutions! We are committed to fostering an inclusive environment that supports your professional growth while contributing to life-changing medical research.
Pay: $18.00 - $21.00 per hour
Benefits:
• Dental insurance
• Health insurance
• Paid time off
• Vision insurance
Work Location: In person
Qualifications
- •Demonstrated ability to coordinate multiple tasks within a clinical research environment
- •Able to communicate fluently in English and Spanish
- •Knowledge of basic clinical trials management, including familiarity with FDA regulations, ICH GCP standards, and CDISC data standards
- •Strong understanding of medical terminology, clinical laboratory procedures, blood sampling techniques, and patient monitoring protocols
- •Experience reviewing documentation for accuracy, completeness, and compliance with regulatory standards such as HIPAA and GCP
- •Proficiency in statistical software tools used for data analysis within clinical research settings
- •Excellent organizational skills with attention to detail; ability to adhere strictly to compliance management protocols
Benefits
- •Pay: $18.00 - $21.00 per hour
- •Dental insurance
- •Health insurance
- •Paid time off
- •Vision insurance
Responsibilities
- •Join our dynamic clinical research team as an Assistant Project Coordinator specializing in Source Documents Building!
- •In this vital role, you will support the management of clinical trial documentation, ensuring accuracy, compliance, and seamless data flow
- •Your proactive approach will help accelerate research progress, uphold regulatory standards, and contribute to groundbreaking medical advancements
- •This paid position offers an exciting opportunity to develop your skills in clinical trials management while making a meaningful impact on patient care and scientific discovery
- •Assist in the collection, review, and organization of source documents for clinical trials, ensuring completeness and adherence to protocol specifications
- •Support the creation and maintenance of source document builder templates aligned with GCP-ICH standards and regulatory requirements
- •Review clinical trial documentation for consistency, accuracy, and regulatory compliance before submission or archiving
- •Contribute to data management efforts by organizing source documents for efficient retrieval and audit readiness
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