Clinical Research Coordinator

Capefox•Bethesda, MD

27d•Onsite

About The Position

Concentric Methods is seeking an experienced Clinical Research Coordinator to independently provide support services to the NIH. The total hourly pay for this non-exempt position is $30.00 for up to 40 hours per week. This rate represents the company’s good faith and reasonable estimate of possible compensation at the time of posting. In addition, for eligible positions we offer a variety of benefits including specified holidays, paid leave, health insurance, dental insurance, vision insurance, life and disability insurance, tuition reimbursement, as well as 401K with company match. This job will be posted until filled or withdrawn.

Requirements

Bachelor's Degree Required
Two years of related experience
Strong organizational and time management skills.
Excellent interpersonal and communication skills.
Attention to detail in data collection and documentation.
Proficiency in relevant computer applications and software.
Ability to work both independently and collaboratively.
Problem-solving and critical-thinking abilities.

Nice To Haves

Manuscript preparation
Data acquisition
Coordinating events
Protocol development
Statistical Analysis
Recruitment
Research
Familiarity with STATA and NVivo

Responsibilities

Supports clinical staff develop, implement and maintain clinical research data files and materials.
Assist preparing and submitting for review accurate source documents related to all research procedures.
Collects research data and prepares information for inputs and analysis.
Work with staff on data acquisition and analysis using a variety of methods, including recruitment, entry, management and display for the Department of Bioethics research studies.
Supports the development of forms and questionnaires.
Work with staff to coordinate the logistics of courses and workshops, including the course Ethical and Regulatory Aspects of Clinical Research, and the Empirical Research Lab.
Supports the collection of data from patient charts, medical records, interviews, questionnaires, and diagnostic tests.
Conduct literature searches; gather and synthesize background information.
Monitors subject's progress and reports adverse events.
Assist staff writing progress reports and contributions to peer-reviewed scientific manuscripts.
Supports the assembly, development and review of new research projects.
Work with staff on manuscript preparation for research studies and manuscript submission.
Prepare materials for IRB submission, manuscript transmittals and other necessary approvals and reviews.
Supports the creation and management of clinical websites and web-based tools.
Collaborate with staff on the maintenance of Departmental metrics, databases and website.