Temporary - Clinical Research Coordinator

Requirements

• Will complete all NIH/NIDA Mandatory trainings or/and other required trainings by the deadline set forth.
• Excellent analytical, organizational and time management skills required.
• Strong communications skills, both oral and written.
• Exceptional interpersonal skills, customer service oriented and client focused approach to work due to extensive participant contact.
• Previous experience in human subjects' interaction (clinical or research).
• Previous clinical trial work
• Deliverables:
• Work products and documents related to administering mental health assessments and diagnostic interviews. - Ad-Hoc
• Work products and documents related to obtaining participant medical and drug use information according to protocol criteria. - Ad-Hoc
• Work products and documents related to obtaining informed consent documentation from participants in the screening protocol. - Ad-Hoc
• Work products and documents related to follow-up correspondence to candidates on recruiting status. - Ad-Hoc
• Work products and documents related to arranging travel and distributing remuneration for candidates. - Ad-Hoc
• Work products and documents related to scheduling phone screen scripts, in person screening appointments and communications with candidates. - Ad-Hoc
• Work products and documents related to data entry in the electronic medical record system., generating reports; perform study procedures; process and destroy specimens as needed; maintain storage records/inventory of biological specimens. - Ad-Hoc
• Statement of Work Details:
• Assist preparing and submitting for review accurate source documents related to all research procedures . - 1
• Participate in developing and maintaining research protocol documentation and operations. - 2
• Assist researchers with study testing, observations data entry and other duties associated with study sessions. - 3
• Supports clinical staff develop, implement and maintain clinical research data files and materials.
• Acquaint participants with the MRI or mock MRI scanner to assess their comfort level, fit and eligibility to participate in MRI studies.
• Collects research data and prepares information for inputs and analysis.
• Verify study participant information and collect data and results of testing.
• Assist staff develop, assemble related documentation and maintain regulatory binders for all protocols.
• Perform accurate and timely data analysis, report results and findings and respond to sponsor queries.
• Set up, format and enter data into spreadsheets to analyze information and create reports.
• Enter data into research databases, systems and applications for ongoing studies.
• Supports the development of forms and questionnaires.
• Assist researchers develop, maintain and complete study data collection forms and source documents.
• Review draft pro

Benefits

Additional Information

(ID: 2026-2380) Axle is a bioscience and information technology company that offers advancements in translational research, biomedical informatics, and data science applications to research centers and healthcare organizations nationally and abroad. With experts in biomedical science, software engineering, and program management, we focus on developing and applying research tools and techniques to empower decision-making and accelerate research discoveries. We work with some of the top research organizations and facilities in the country including multiple institutes at the National Institutes of Health (NIH). Axle is seeking a Clinical Research Coordinator (Temporary - Approximately 4 Months) to join our vibrant team at the National Institutes of Health (NIH) in Baltimore, MD. This position will support ongoing clinical research activities within the National Institute on Drug Abuse (NIDA) and offers an opportunity to contribute to cutting-edge behavioral and clinical research initiatives. Benefits We Offer: 100% Medical, Dental & Vision Coverage for Employees Paid Time Off and Paid Holidays 401K match up to 5% Educational Benefits for Career Growth Employee Referral Bonus Flexible Spending Accounts: Healthcare (FSA) Parking Reimbursement Account (PRK) Dependent Care Assistant Program (DCAP) Transportation Reimbursement Account (TRN) Position Information: Under this task order, the contractor will independently provide support services to satisfy the overall operational objectives of the National Institute on Drug Abuse. The primary objective is to provide services and deliverables through performance of support services. Additional Qualifications Certifications & Licenses: Minimum of one (1) year of experience in behavioral counseling, preferably in drug/smoking/alcohol treatment. Minimum of three (3) years of experience in a research related field. Master's degree in psychology, social work, biological sciences or related discipline. Basic Life Support (BLS) certification will be required - training will be provided. Field of Study: Social Work (Required) Software: Proficient computer skills required (e.g. Microsoft Office)

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