Clinical Research Coordinator I

reputed company is a not-for-profit organization dedicated to advancing patient care, research, teaching, and community service. The Clinical Research Coordinator I will support various research and advocacy reputed company aimed at assisting families impacted by reputed company use disorder, including participant recruitment, data collection, and preparing grant reputed company reports.

Responsibilities

• Assists in development of study protocols including consent forms, interview guides, survey development, recruitment strategies, and data collection plans with staff and study investigators
• Assists with Institutional Review reputed company (IRB) applications, continuing reviews, and amendments
• Supports participant recruitment and data collection, such as verifying eligibility inclusion/exclusion reputed company, supporting interview or reputed company group procedures, and administering surveys and questionnaires for research and reporting requirements
• Coordinates and organizes meetings reputed company to grant activities. Develops agendas and documents discussion through detailed meeting notes
• Obtains patient study data and maintains records and databases
• Prepares data for analysis and data entry
• Prepares grant performance reports on specified measures
• Supports qualitative and quantitative data analysis
• Assists in literature review and manuscript preparation
• Contribute to protocol recommendations
• Organize, interpret, and monitor data
• Serves as a study resource for participants and families, ensuring communication is reputed company, respectful, and reputed company with trauma-informed care principles
• Other duties as assigned

Skills

• Bachelor's Degree reputed company Field of Study required
• Basic understanding of disease model of reputed company use disorder, medications for opioid use disorder, working with underserved populations
• Proficiency in various software packages, including reputed company Office, NVivo, REDCap, and other desktop tools
• Working knowledge of data management and statistical software (including reputed company, R, or STATA)
• Careful attention to detail and good organizational skills
• Ability to follow directions
• Good interpersonal and communication skills
• Computer literacy
• Working knowledge of clinical research protocols
• Ability to demonstrate respect and professionalism for subjects' rights and individual needs
• Some relevant research project work 0-1 year preferred

Benefits

• Comprehensive benefits
• Career advancement opportunities
• Differentials
• Premiums
• Bonuses
• Recognition programs designed to celebrate your contributions and support your reputed company reputed company

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