Clinical Research Coordinator providing assistance on clinical research studies including recruiting and organizing data. Supporting patient consent and clinical tests within a hybrid work setting.
Responsibilities
Provides assistance on clinical research studies, including recruiting, evaluating, and consenting patients for studies
Collecting and organizing patient data
Scheduling patients for study visits
Performing clinical tests such as phlebotomy, EKGs, etc.
Maintaining and updating data generated by the study
Reviewing proposals for compliance with sponsor and organizational guidelines
Verifying that all sponsor requirements are met
Conducting phone interviews to recruit patients for clinical trials
Verifying the accuracy of study forms and updating them per protocol
Preparing data for analysis and data entry
Documenting patient visits and procedures
Assisting with regulatory binders and QA/QC Procedures
Assisting with interviewing study subjects
Assisting with study regulator submissions
Requirements
Bachelor's Degree Related Field of Study required
Some relevant research project work 0-1 year preferred
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.
Benefits
competitive base pay
comprehensive benefits
career advancement opportunities
differentials
premiums
bonuses as applicable
recognition programs designed to celebrate your contributions and support your professional growth
Senior Clinical Trial Manager leading global clinical trials for Disc Medicine. Focused on project management and vendor oversight within a hybrid work environment.
Manager overseeing Project Management team in Clinical Research at Sanford Health. Collaborating with Clinical Research Managers and guiding strategic research initiatives.
Research Coordinator overseeing clinical studies for musculoskeletal injuries in military health. Assisting with project planning and coordination while ensuring compliance with protocols and regulations.
Overseeing and administering clinical research studies and managing study budgets for military health research. Coordinating project planning and ensuring compliance with regulatory requirements.
Centralized Clinical Trial Manager at ICON responsible for reviewing clinical trial site visit reports and ensuring quality standards. Act as a liaison for timely resolution of issues.
Clinical Research Nurse Coordinator managing clinical research operations at Duke's Trauma, Acute & Critical Care Division. Supervising nursing care and ensuring accuracy in data management.
Clinical Research Coordinator managing clinical trials at Emory University. Overseeing research projects, providing guidance, and ensuring compliance with protocols and regulations.
Senior Clinical Trial Manager managing Phase 1 clinical research studies and collaborating with cross - functional teams in a global biopharmaceutical environment.
HR Manager for Clinical Research Units lead engagement strategies at Fortrea. Partnering closely with site leadership in clinical environments in Dallas, TX or Madison, WI.