Clinical Research Coordinator

Cedar Health Research; Euless (TX); On-site; USD 55,000 - 80,000; Full time

Job summary

Cedar Health Research is seeking a Clinical Research Coordinator to oversee and conduct clinical trials. The ideal candidate will have at least 3 years of experience and a medical background, along with excellent interpersonal and organizational skills. Responsibilities include managing trial operations, training staff, and ensuring compliance with regulatory requirements. This position offers a competitive salary and a chance to contribute to impactful research.

Qualifications

• At least 3 years of experience as a clinical research coordinator, preferably on phase II & III studies.
• Trained or willing to be trained in phlebotomy, vital signs, medical history collection, and EKGs.

Responsibilities

• Oversee the smooth running of clinical trials at the site in collaboration with study investigators and team members.
• Conduct proper consenting of research participants and monitor their compliance.
• Supervise and train research staff, including coordinators and assistants.

Skills

Interpersonal skills

Communication

Organizational skills

Attention to detail

Job description

Join to apply for the Clinical Research Coordinator role at Cedar Health Research.

Get AI-powered advice on this job and more exclusive features.

Position Description

Experienced candidates with medical backgrounds and excellent interpersonal skills are encouraged to apply for the Clinical Research Coordinator (CRC) position. This role is responsible for the successful conduct of clinical trials under the oversight of the principal investigator. The CRC will handle both clinical and administrative duties related to clinical research at the site.

Job Responsibilities

• Abide by local, state, GCP, ICH, and FDA guidelines and regulations for clinical trials.
• Oversee the smooth running of clinical trials at the site in collaboration with study investigators and team members.
• Complete all required organization and study-specific training promptly, including offsite investigator meetings.
• Supervise and train research staff, including study coordinators, research assistants, and lab technicians.
• Participate in planning and conducting participant recruitment efforts.
• Conduct proper consenting of research participants.
• Collect source data and transcribe into case report forms.
• Perform clinical procedures such as vital signs, EKG, and phlebotomy.
• Process study labs as required.
• Provide training and mentorship to the study team.
• Collaborate with sponsor/CRO study teams, resolving queries promptly.
• Monitor participants for adherence and compliance.
• Perform inventory checks and ensure supplies and equipment are in stock and functional.
• Engage with subjects and address their concerns.

Qualification Requirements

• At least 3 years of experience as a clinical research coordinator, preferably on phase II & III studies.
• Trained or willing to be trained in phlebotomy, vital signs, medical history collection, and EKGs.
• Attention to detail.
• Excellent interpersonal, communication, and organizational skills.
• Willingness to self-educate continually.