Clinical Research Coordinator - Germantown, TN
Arlington, TNFull-time
Behavioral Health Market Context
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Job Description
its, processing laboratory samples, and performing ambulatory blood pressure monitor (ABPM) procedures. Accurate and timely data entry will be an essential part of this role.
Responsibilities
• Perform a variety of complex clinical procedures, including ECG, spirometry, sample collection, and vital signs.
• Phlebotomy is required; pediatric experience is highly preferred.
• Coordinate clinical research studies and maintain compliance with protocols and Good Clinical Practice (GCP) guidelines.
• Conduct patient consenting and perform study visits in accordance with study protocols.
• Process laboratory samples and perform ABPM (ambulatory blood pressure monitor) procedures.
• Support study conduct by preparing study materials, setting up equipment, and planning logistical activities.
• Recruit, screen, and orient volunteers, ensuring their safety and well-being throughout the study.
• Collect and accurately record clinical data in case report forms (CRFs); complete timely and high‑quality data entry.
• Collaborate with investigators and monitors, addressing queries and ensuring data quality.
• Act as a volunteer advocate and maintain a safe environment in accordance with Health and Safety policies.
Requirements
• High School Diploma or equivalent education and experience.
• Minimum 1 year of relevant work experience in clinical research (preferred).
• Working knowledge of clinical trials, GCP principles, and medical terminology.
• Strong attention to detail and ability to establish effective working relationships.
Nice-to-haves
• Experience with CRIO is a plus.
• Experience with Allscripts/Altera EMR is a plus.
Responsibilities
• Perform a variety of complex clinical procedures, including ECG, spirometry, sample collection, and vital signs.
• Phlebotomy is required; pediatric experience is highly preferred.
• Coordinate clinical research studies and maintain compliance with protocols and Good Clinical Practice (GCP) guidelines.
• Conduct patient consenting and perform study visits in accordance with study protocols.
• Process laboratory samples and perform ABPM (ambulatory blood pressure monitor) procedures.
• Support study conduct by preparing study materials, setting up equipment, and planning logistical activities.
• Recruit, screen, and orient volunteers, ensuring their safety and well-being throughout the study.
• Collect and accurately record clinical data in case report forms (CRFs); complete timely and high‑quality data entry.
• Collaborate with investigators and monitors, addressing queries and ensuring data quality.
• Act as a volunteer advocate and maintain a safe environment in accordance with Health and Safety policies.
Requirements
• High School Diploma or equivalent education and experience.
• Minimum 1 year of relevant work experience in clinical research (preferred).
• Working knowledge of clinical trials, GCP principles, and medical terminology.
• Strong attention to detail and ability to establish effective working relationships.
Nice-to-haves
• Experience with CRIO is a plus.
• Experience with Allscripts/Altera EMR is a plus.
Qualifications
- •High School Diploma or equivalent education and experience
- •Working knowledge of clinical trials, GCP principles, and medical terminology
- •Strong attention to detail and ability to establish effective working relationships
Benefits
Responsibilities
- •We are seeking a Clinical Research Coordinator (CRC) to join our team and support clinical research studies under the supervision of a principal investigator
- •This role involves hands-on clinical procedures, community outreach, and ensuring the highest standards of care and compliance
- •Responsibilities also include working directly with consenting patients, conducting study visits, processing laboratory samples, and performing ambulatory blood pressure monitor (ABPM) procedures
- •Accurate and timely data entry will be an essential part of this role
- •Perform a variety of complex clinical procedures, including ECG, spirometry, sample collection, and vital signs
- •Phlebotomy is required; pediatric experience is highly preferred
- •Coordinate clinical research studies and maintain compliance with protocols and Good Clinical Practice (GCP) guidelines
- •Conduct patient consenting and perform study visits in accordance with study protocols
- •Process laboratory samples and perform ABPM (ambulatory blood pressure monitor) procedures
- •Support study conduct by preparing study materials, setting up equipment, and planning logistical activities
- •Recruit, screen, and orient volunteers, ensuring their safety and well-being throughout the study
- •Collect and accurately record clinical data in case report forms (CRFs); complete timely and high‑quality data entry
- •Collaborate with investigators and monitors, addressing queries and ensuring data quality
- •Act as a volunteer advocate and maintain a safe environment in accordance with Health and Safety policies
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