Research Coordinator-Endocrinology
About The Position
The Research Coordinator-Endocrinology will be responsible for providing clinical care services, including consenting, treating, and monitoring patients. This role involves recruiting and screening candidates for clinical trials, acquiring medical and medication history, processing and shipping biological samples, and dispensing research drugs according to protocol. The coordinator will utilize electronic systems for patient information, prepare for audits, and perform various research, data entry, and regulatory duties. They will ensure adherence to protocols, assist with budget proposals and tracking expenditures, and complete regulatory submissions for the Institutional Review Board (IRB). Communication and coordination with physicians and study personnel are essential for study design, implementation, and completion. The role also includes data abstraction, data entry, and timely reporting of adverse events.
Requirements
- HS Diploma Required
- 1-5 years of research experience
- Computer literacy in Microsoft Word, Excel, Power Point
- Excellent interpersonal skills and the ability to interact in a professional and sensitive manner handling financial information, research project information, research proposals, IRB paperwork.
- Excellent organizational skills and attention to detail
Nice To Haves
- Bachelor’s degree preferred, in the fields of social, biological or healthcare sciences preferred
- Familiarity with clinical data is preferable.
- Experience with phlebotomy, ECG and pharmacy practices preferred
- CCRP or CCRC; CITI Good Clinical Practice, Human Subjects Research and IATA; preferred
Responsibilities
- Provides clinical care services including consenting, treating and monitoring of patients
- Recruit and screen candidates for clinical trials
- Acquire past medical and medication history profiles
- Obtain, process and ship biological lab samples
- Dispense research drug to patients according to protocol.
- Utilize electronic capture to submit and update patient information.
- Prepare for routine audits and oversight visits
- Perform a variety of research, data entry and regulatory duties of a routine and technical nature within the required time frames
- Ensure adherence to protocols and quality of information received
- Identifying and screening study participants, enroll subjects to the trials in adherence with the protocol
- Assist with developing study budget proposals and tracking study expenditures
- Assist with study time reporting
- Ensure compliance with local, state and Federal regulations for the protection of human subjects
- Complete regulatory submissions/revisions for the Institutional Review Board (IRB)
- Communicate and coordinate with physicians, division staff, and other departmental study personnel as required for study design, implementation and completion
- Complete data abstraction and data entry for study specific databases.
- Review and timely report study related adverse events to the sponsor.
Benefits
- Premium pay such as shift, on call, holiday and more based on an employee’s job (For eligible positions)
- Incentive pay for select positions
- Opportunity for annual increases based on performance
- Career Pathways to Promote Professional Growth and Development
- Various Medical, Dental, Pet and Vision options
- Tuition Reimbursement
- Free Parking
- Wellness Program
- Savings Plan
- Health Savings Account Options
- Retirement Options with Company Match
- Paid Time Off and Holiday Pay
- Community Involvement Opportunities
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED
