- Review of patient's records to screen for eligibility
- Call potential patients to discuss study
- Schedule/ Reschedule appointments for study patients
- Prepare patient charts
- Assist with input of clinical exams into EDC
- Assist with clinical exams as needed
- Assist with collection of required paperwork
- Correspond with PCPs as necessary
- Assist with end of study paperwork
- Phlebotomy skills
- Screening assessments
- Medical Insurance
- Vision Insurance
- Dental Insurance
- 401(k)
- Life Insurance & Short and Long-Term Disability
- PTO
- Houston, TX 77058: Reliably commute or planning to relocate before starting work (Required)
- Travel during the workday also required
- Phase II - IV in-patient/out-patients clinical studies
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Clinical Research Coordinator - Houston, United States - Boson Health
Description
As part of our continued growth, aQua Research Institute, LLC. has made a significant commitment to expanding our involvement in clinical research studies. This commitment has led to the creation of the Clinical Research Coordinator position.This is a full-time, Monday through Friday position with 8 hour dayshifts only.
Under the direct supervision of the Principal Investigator and Clinical Research Manager, the ideal candidate will perform assigned activities related to clinical research studies.
The ideal candidate will be an experienced clinical research coordinator highly driven, self-motivated and eager to work both independently as well as be part of a dynamic team.
Must be reliable, detail oriented, have advanced organizational and planning skills as well as be people-oriented. Must have the ability to assist with multiple projects and manage time effectively.
Must be flexible and have an understanding that their job description and responsibilities can change as the role is developed.
Job tasks will include but not be limited to:offers a competitive wage & benefits package for full-time eligible employees that includes:
Job Type:
Full-time
Pay Rate starting:
$25.00
Ability to commute/relocate:
Experience:
Clinical Research Coordinator: 3 years experience in Phase 2 and 3 sponsor initiated trials