Clinical Research Coordinator

Elevate Clinical Research is hiring a Clinical Research Coordinator to coordinate and manage clinical trials in healthcare settings. The role oversees recruitment, consent, study visits, regulatory compliance, study documentation, data integrity, patient safety, and collaboration with investigators, sponsors, and study teams.

Responsibilities

Coordinate and oversee the daily operations of clinical trials, including patient recruitment, informed consent, and scheduling study visits

Ensure compliance with all regulatory requirements, institutional policies, and Good Clinical Practice (GCP) guidelines throughout the study lifecycle

Maintain accurate and up-to-date regulatory documents, case report forms, and study databases to support data integrity and audit readiness

Monitor study progress and patient safety by conducting regular assessments and reporting adverse events to the appropriate parties

Collaborate with investigators, sponsors, and multidisciplinary teams to facilitate effective communication and resolve study-related issues promptly

Preferred

Certification as a Clinical Research Coordinator (e.g., ACRP-CRC or SOCRA)

Experience working with electronic data capture (EDC) systems and clinical trial management systems (CTMS)

Advanced knowledge of FDA regulations and Institutional Review Board (IRB) processes

Previous experience in patient recruitment and retention strategies for clinical studies

Master's degree in Clinical Research, Public Health, or a related discipline

Preferred skills like experience with electronic data systems and advanced regulatory knowledge enhance the ability to manage complex data and navigate regulatory landscapes

Clinical Research Coordinator Certification

Electronic Data Capture (EDC)

Clinical Trial Management Systems (CTMS)

FDA Regulations

Institutional Review Board (IRB) Processes

Patient Retention Strategies

Clinical Study Management

Electronic Data Systems

Public Health

Benefits

Clear, structured onboarding

Leadership that listens and supports

Career growth as we expand into new states

Company

Clinical trials and medical research services.

Houston, Texas, USA

https://www.elevateclinical.com/

Founded in 2024

51-200 employees

Qualifications

Bachelor's degree in a health-related field such as Nursing, Life Sciences, or Public Health

At least 2 years of experience coordinating clinical research studies or trials

Comprehensive knowledge of clinical trial processes, regulatory requirements, and ethical standards

Familiarity with clinical research documentation, including informed consent forms and case report forms

Strong organizational skills and attention to detail to manage multiple study activities simultaneously

The required skills such as clinical trials coordination, regulatory document management, and patient recruitment are essential for ensuring that studies are conducted efficiently and ethically

Clinical monitoring and trial management skills enable the coordinator to oversee study progress and maintain compliance with protocols and regulations

Proficiency in clinical research and clinical practice allows the coordinator to understand medical terminology and patient care considerations, facilitating effective communication with healthcare providers and participants

Certification as a Clinical Research Coordinator (e.g., ACRP-CRC or SOCRA)

Experience working with electronic data capture (EDC) systems and clinical trial management systems (CTMS)

Advanced knowledge of FDA regulations and Institutional Review Board (IRB) processes

Previous experience in patient recruitment and retention strategies for clinical studies

Master's degree in Clinical Research, Public Health, or a related discipline

Preferred skills like experience with electronic data systems and advanced regulatory knowledge enhance the ability to manage complex data and navigate regulatory landscapes

At least 2 years of experience coordinating clinical research studies or trials.

Required skills

Clinical Trial Coordination, Clinical Research, Regulatory Compliance, Clinical Research Documentation, Informed Consent, Case Report Forms, Patient Recruitment and Retention, Clinical Monitoring, FDA Regulations, Institutional Review Board (IRB) Processes, ACRP-CRC, SOCRA Certification

Experience

2+ years