Clinical Research Associate (CRA)

Healing Kidneys Institute Of Housto; Conroe (TX); On-site; USD 45,000 - 60,000; Full time

Benefits offered by this job

Bonus based on performance

Company parties

Flexible schedule

Profit sharing

Job summary

A clinical research organization in Conroe, Texas seeks a full-time Clinical Research Coordinator. The ideal candidate will possess certification as a Medical Assistant or Phlebotomy and exhibit a strong passion for direct patient care. Responsibilities include conducting patient screenings and managing IRB protocols while ensuring compliance and maintaining high data integrity. Join our team to contribute meaningfully to patient outcomes in nephrology and rare diseases.

Qualifications

• A qualified candidate with certification as an MA, phlebotomy, or similar.
• Skilled in conducting IRB approved clinical trial protocols.
• Ability to perform direct patient care activities.

Responsibilities

• Conduct patient screenings, randomization, and enrollment.
• Perform direct patient care activities like blood draws and ECG.
• Ensure regulatory compliance and maintain protocol adherence.

Skills

Patient interaction

IRB protocol execution

Attention to detail

Communication skills

Education

Certification as an MA or Phlebotomy

Job description

Benefits

• Bonus based on performance
• Company parties
• Flexible schedule
• Profit sharing

Our clinical research group is looking to hire a qualified candidate for the full-time position of Clinical Research Coordinator. The ideal candidate will possess certification such as an MA, phlebotomy, or similar and have a strong desire to work directly with patients.

Who We Are

Healing Kidneys Clinical Research is a Nephrology clinical trials focused company in Rare disease space that uses proprietary technology to: Increase patient access to research trials within our communities,

Deliver superior clinical research enrollment metrics to Pharma sponsors

All with the goal of Improving Patient Outcomes at the Point of Care. We want you to join us in doing just that.

Desirable Candidate

• A lover of patient interaction and skilled at providing patient care
• A team player with a bias for action and an attitude that takes personal responsibility
• Skilled in all aspects required for conducting an IRB approved clinical trial protocol: identification, screening, randomization, and enrollment of patients, conducting clinic visits, etc.
• Skilled at performing and assisting with direct patient care activities: consenting patients, physical assessments, blood draws, medication administration, ECG, etc.
• Possess an acute attention to detail for clean data entry, regulatory compliance, productive site visits, efficient study set-up and maintenance, and strict protocol adherence
• An expert communicator with the goal of fostering relationships between the research team, PIs, Sponsors, Monitors, and others
• Not easily distracted: You have the ability to stay focused while running different protocols, resolving and submitting IRB responses and audit findings, tracking AE and SAE events, and maintaining eSource material for assigned studies

Energized by the idea of playing a role in the future of new therapy development in Nephrology & Rare diseases