Clinical Research Coordinator Ii-relocation Support Provided
Careaccess
Dallas, United States
On-site
Good clinical practices gcp knowledge
Fda regulations and ich guidelines adherence
Patient screening and informed consent
The role involves utilizing Good Clinical Practices to screen, enroll, and monitor clinical research study subjects while ensuring protocol compliance
Job Summary
The role involves utilizing Good Clinical Practices to screen, enroll, and monitor clinical research study subjects while ensuring protocol compliance.
Candidates will be responsible for identifying adverse events, obtaining informed consent, and coordinating pre-study and site initiation visits.
Care Access is dedicated to making advanced health screenings and research opportunities accessible to communities worldwide through world-class research.
Matching Summary
The role involves utilizing Good Clinical Practices to screen, enroll, and monitor clinical research study subjects while ensuring protocol compliance.
Skills & Requirements
Must-have
Good Clinical Practices GCP knowledge
FDA regulations and ICH guidelines adherence
Patient screening and informed consent
Adverse event identification and reporting
Source data entry and query resolution
Nice-to-have
Effective relationship building with patients
Positive professional interaction skills
Ability to train others on procedures
Experience with clinical study visits
Strong organizational and time management
Key Requirements
Knowledge of FDA regulations and ICH guidelines
Experience with clinical trial protocols
Ability to perform basic clinical procedures like blood draws