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.

Candidate should have the ability to evaluate a patient's medical record for eligibility and recruitment. Candidate must have excellent verbal, written, and interpersonal communication skills.

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:

· 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

aQua Research Institute, LLC. offers a competitive wage & benefits package for full-time eligible employees that includes:

• Medical Insurance
• Vision Insurance
• Dental Insurance
• 401(k)
• Life Insurance & Short and Long-Term Disability
• PTO

Job Type: Full-time

Pay Rate starting: $25.00

Ability to commute/relocate:

• Houston, TX 77058: Reliably commute or planning to relocate before starting work (Required)
• Travel during the workday also required

Experience:

• Clinical Research Coordinator: 3 years experience in Phase 2 and 3 sponsor initiated trials
• Phase II - IV in-patient/out-patients clinical studies