Clinical Research Coordinator

Cape Fox Corporation; Bethesda (MD); On-site; USD 53,040 - 71,760; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

Life insurance

Disability insurance

Tuition reimbursement

401K match

Paid holidays

Paid leave

Job summary

Concentric Methods is seeking an experienced Clinical Research Coordinator to independently support NIH-related studies. Duties include data file maintenance, source document preparation, data collection, and coordination of research logistics.

The role emphasizes regulatory compliance, manuscript preparation, and collaboration with clinical staff to ensure data integrity and timely reporting. Travel is limited and the position is onsite in Bethesda, MD.

Qualifications

• Bachelor's degree required; two years related experience preferred.
• Familiarity with STATA and NVivo is beneficial.
• Experience in clinical research coordination and data management.
• Ability to work independently and collaboratively in a team.

Responsibilities

• Supports clinical staff in developing, implementing and maintaining clinical research data files and materials.
• Assists with preparing and submitting accurate source documents related to all research procedures.
• Collects research data and prepares information for inputs and analysis.
• Works with staff on data acquisition and analysis using recruitment, entry, management and display for bioethics studies.
• Supports the development of forms and questionnaires.
• Coordinates logistics of courses and workshops, including the Ethical and Regulatory Aspects of Clinical Research.
• Supports collection of data from patient charts and source documents.
• Monitors progress and reports adverse events.
• Assists in writing progress reports and manuscripts for peer-reviewed journals.

Skills

Clinical research

Data management

IRB submissions

Regulatory compliance

Education

Bachelor's Degree

2 years related experience

Tools

STATA

NVivo

Job description

Clinical Research Coordinator

Job Description

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.

Responsibilities

• Supports clinical staff in developing, implementing and maintaining clinical research data files and materials.
• Assists with preparing and submitting accurate source documents related to all research procedures.
• Collects research data and prepares information for inputs and analysis.
• Works 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.
• Coordinates 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.
• Conducts literature searches; gathers and synthesizes background information.
• Monitors subjects’ progress and reports adverse events.
• Assists staff in writing progress reports and contributions to peer-reviewed scientific manuscripts.
• Supports assembly, development and review of new research projects.
• Works with staff on manuscript preparation for research studies and manuscript submission.
• Prepares materials for IRB submission, manuscript transmittals and other necessary approvals and reviews.
• Supports the creation and management of clinical websites and web-based tools.
• Collaborates with staff on the maintenance of departmental metrics, databases and website.

Travel Requirements

0 - 10%

Preferred Professional Experience

• Manuscript preparation
• Data acquisition
• Coordinating events
• Protocol development
• Statistical analysis
• Recruitment
• Research

Familiarity with STATA and NVivo

Education and Certifications

• Bachelor's Degree Required
• Two years of related experience

Core Skills

• 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.

Location

Bethesda, MD - Bethesda, MD 20892 US (Primary)