What are the responsibilities and job description for the Clinical Protocol Coordinator position at Columbus Technologies?
Must be a US Citizen
W2 with full benefits
Offer contingent on ability to successfully pass a background check and drug screen
Columbus Technologies and Services Inc. is a strategic supplier and business partner to the federal government and its key suppliers. Through our partnership with the National Institutes of Health, Columbus offers administrative, IT, engineering, scientific, and healthcare professionals the opportunity to work with one of the most prestigious research organizations in the world. We are currently seeking a Clinical Protocol Coordinator to work onsite with the National Institutes of Health in Bethesda, MD.
This is a long-term position which offers:
- Competitive salary
- Tremendous growth opportunity
- Opportunity to work at NIH, the world's foremost medical research center
- Learn more about what Columbus can do for you at www.columbususa.com
The US base salary for this full-time position is $24.50-61/hr benefits. Salary ranges are determined by role, level, and location. The range displayed on each job posting reflects the minimum and maximum target for new hire salaries for the position across all US locations. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training.
Responsibilities
The Translational Immunopsychiatry Unit (TIU) is seeking an ambitious, conscientious, organized, and detail-oriented Clinical Research Coordinator (CRC) with strong interpersonal and communication skills to join our growing team at the National Institutes of Health (NIH). This CRC position will be supporting the National Institute of Mental Health (NIMH), located in Bethesda, MD. The primary responsibilities for this full-time on-site CRC position will be to provide clinical and biospecimen research coordination for the TIU and affiliated programs, including the Autoimmune Brain Disorders Program (ABDP).
• Supports clinical staff develop, implement and maintain clinical research data files and materials
• Collects research data and prepares information for inputs and analysis.
• Supports the development of forms and questionnaires.
• Supports the collection of data from patient charts, medical records, interviews, questionnaires, and diagnostic tests.
• Monitors subject's progress and reports adverse events.
• Supports assembly, development and review of new research projects.
• Supports the creation and management of clinical websites and web-based tools.
• Organizes and performs clinical research, utilizing internet and other available clinical resources.
• Provides assistance to staff in the collection, development and quality control of essential clinical research efforts.
• Supports clinical staff develop, implement and maintain clinical research data files and materials.
• Develops and facilitates training to new research coordinators and mentors researchers in Good Clinical Practices.
Qualifications
Required Skills:
• Bachelor’s degree in Microbiology, Molecular Biology, or related field
• Biomedical Research Informatics Cumputing System
• Biomedical Translational Research Informatics
• Lab Archives
• Ordering, tracking, and managing IP and trial materials
• Implementation of clinical trial site action plans
• Coordinating project meetings
Equal Opportunity/Affirmative Action:
We are committed to hiring and retaining a diverse workforce. All qualified applicants will receive consideration for employment without regard to race, color, religion, creed, sex, sexual orientation, gender identity or expression, marital status, age, national origin, veteran status, disability status, or any other protected class. EEO/AA/MFDV
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Salary : $25 - $61
