Clinical Research Coordinator

Monument Health Rapid City Hospital•Rapid City, SD

4d•$23 - $29•Onsite

About The Position

Clinical Research Coordinator is responsible for the full implementation and management of trials in direct collaboration with administrative and clinical leadership, investigators, sponsors and clinical research organizations. Establish and maintain effective working relationships with team members, extended health care providers, clinical research organizations, and regulatory agencies to ensure the safe and effective care of those who volunteer to be participants in clinical research. Monument Health offers competitive wages and benefits on qualifying positions. Some of those benefits can include: 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

Requirements

Education - High School Diploma/GED Equivalent
Certification - Within 30-days of hire - Human Subject Protection (HSP) - Collaborative Institutional Training Initiative (CITI); OR Good Clinical Practice (GCP) - Collaborative Institutional Training Initiative (CITI)

Nice To Haves

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

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.