Clinical Research Coordinator jobs in United States
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Monument Health · 5 hours ago

Clinical Research Coordinator

Monument Health is seeking a Clinical Research Coordinator responsible for the full implementation and management of clinical trials. This role involves collaboration with various stakeholders to ensure the safety and effective care of clinical research participants.

Health CareHospitalNon ProfitRehabilitation

Responsibilities

Assist in developing source document templates in Microsoft Word, Excel, or similar program. Source documents should be routinely maintained to reflect accurate information that is required of sponsors by verifying against eCRF software
Completes relevant data collection, entry and analysis as and when needed
Coordinates the efforts of case finding and recruitment of study patients
Create, organize, submit, and maintain all pertinent study documents, records, and logs from start-up to study closure between sponsor and other offices. Documents include regulatory documents, contracts, temperature logs, budgets, licenses, training documentation, etc
Creates and maintains study and subject specific case report forms. Develop data collection worksheets that ensure complete collection of data which can be accurately transmitted by data entry staff
Demonstrates the ability to work in collaboration with other members of the Clinical Research Team to provide safe quality care to our subject population and efficiently complete daily responsibilities which include but not limited to the following: Develop documents and processes for successful trial implementation which are consistent with internal processes and procedures, regulatory requirements, and 'Good Clinical Practice.' Facilitate site monitoring visits by assuring they have all the information and materials needed to effectively perform their job, assisting them while on site, close-out visit with investigator, addressing action items in monitoring letter. Follows study protocol in scheduling of tests, procedures, and administration of medications. Implement effective study-specific screening, enrollment, and follow-up processes
All other duties as assigned

Qualification

Human Subject Protection CertificationClinical Practice CertificationClinical Research Coordinator CertificationHealthcare ExperienceMicrosoft WordMicrosoft ExcelData CollectionCollaboration

Required

Certification - Human Subject Protection (HSP) - Collaborative Institutional Training Initiative (CITI); OR Good Clinical Practice (GCP) - Collaborative Institutional Training Initiative (CITI)

Preferred

Education - Bachelors degree in Healthcare
Experience - 3+ years of Healthcare Experience
Certification - Clinical Research Coordinator Certification - Accredited University or accredited training professionals

Benefits

Supportive work culture
Medical, Vision and Dental Coverage
Retirement Plans, Health Savings Account, and Flexible Spending Account
Instant pay is available for qualifying positions
Paid Time Off Accrual Bank
Opportunities for growth and advancement
Tuition assistance/reimbursement
Excellent pay differentials on qualifying positions
Flexible scheduling

Company

Monument Health

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Monument Health is a community-based health care system that provides a wide range of treatment and medical services to various patients.

Funding

Current Stage
Late Stage

Leadership Team

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Paulette Davidson, FACHE, CMPE
President & CEO
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Mark Thompson
CFO
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