Details:
- Compensation: $30 - $32/hour
- Benefits: Medical, Dental, Vision
- Employment Classification: Contract To Hire
- Status: On-Site
- Job ID: 21827
Clinical Study Coordinator
Work Location:
Douglas County, Nebraska
Summary:
The Clinical Study Coordinator is responsible for supporting and coordinating clinical research activities, assisting with project management, and ensuring the smooth implementation of clinical trials. This role provides data management support and works to achieve enrollment goals for clinical studies.
Responsibilities:
- Coordinate and manage clinical research activities, ensuring compliance with study protocols and regulatory requirements.
- Assist principal investigators and nurse coordinators with the planning, organization, and execution of clinical trials.
- Support data management processes, including data entry, verification, and maintenance of study records.
- Monitor study progress and work to achieve participant enrollment targets.
- Communicate effectively with research team members and study participants to facilitate study operations.
- Maintain accurate and organized documentation related to clinical trials and research activities.
- Utilize computer applications such as Microsoft Excel, Word, and Outlook for daily tasks and reporting.
- Apply knowledge and skills to meet the needs of adult and geriatric patient populations involved in clinical studies.
Qualifications:
- Bachelor's degree or equivalent combination of education and experience (six years education and/or related experience combined, with at least two years post high school education).
- Minimum of 2 years of clinical or research experience in a clinical or laboratory setting.
- Proficiency in Microsoft Excel, Word, and Outlook required; experience with Microsoft Access and EPIC One Chart preferred.
- Strong communication and interpersonal skills.
- Ability to work collaboratively with team members.
- Excellent organizational skills and attention to detail.
- Demonstrated computer literacy and proficiency.
- Experience with clinical research processes and knowledge preferred.
- Ability to address the needs of adult (18-65) and geriatric (65+) patient populations.
Published Category:
Clinical Operations & Development



