Clinical Trial Researcher - Dallas - CEDENT
Dallas, TX
About the Job
Job description
Minimum Education And Experience
Preferred Education and Experience
• Bachelor's degree in health sciences, neuroscience, psychology, communication sciences and disorders, biomedical engineering, or a related field plus at least 5 years' experience with clinical trials or clinical research in neuroscience, psychology, communication sciences and disorders, biomedical engineering, or a related field.
• Previous experience as a clinical research coordinator, clinical research associate, or related role is preferred.
• Strong interpersonal and conversational skills are required. Must be able to communicate effectively, both verbally and in writing.
• Experience with data management software systems, REDCap or similar, is highly desirable.
Essential Duties And Responsibilities
• Provide trial record management, data management, clinical regulatory functions, and serve as a point of contact for clinical trials; facilitate patient participation in clinical trials.
• Provide education and training to faculty and staff conducting clinical trials.
• Activities may include providing assistance with establishing and maintaining trial regulatory files, coordinating FDA and IRB filings, establishing and maintaining electronic data systems to facilitate data capture and storage across multiple trial sites, site startup and closeout activities, maintaining trial participant records, and assisting with periodic internal site audits for multiple clinical trials.
• Additional duties may include the development and execution of recruiting strategies, management of ClinicalTrials.gov postings, general site coordination and quality control activities, and serving as a resource and mentor for study team members new to the clinical trials research environment.
• Position requires problem-solving and the ability to work independently; participation in regular meetings with researchers; regular and timely coordination of information between patients, clinical, and pre-clinical research teams; and will include providing assistance creating and maintaining constructive collaborations with outside researchers.
Minimum Education And Experience
- Bachelor's degree in health sciences, neuroscience, biomedical engineering, or a related field plus at least one year experience with clinical trials or research in biomedical engineering, neuroscience, or a related field.
Preferred Education and Experience
• Bachelor's degree in health sciences, neuroscience, psychology, communication sciences and disorders, biomedical engineering, or a related field plus at least 5 years' experience with clinical trials or clinical research in neuroscience, psychology, communication sciences and disorders, biomedical engineering, or a related field.
• Previous experience as a clinical research coordinator, clinical research associate, or related role is preferred.
• Strong interpersonal and conversational skills are required. Must be able to communicate effectively, both verbally and in writing.
• Experience with data management software systems, REDCap or similar, is highly desirable.
Essential Duties And Responsibilities
• Provide trial record management, data management, clinical regulatory functions, and serve as a point of contact for clinical trials; facilitate patient participation in clinical trials.
• Provide education and training to faculty and staff conducting clinical trials.
• Activities may include providing assistance with establishing and maintaining trial regulatory files, coordinating FDA and IRB filings, establishing and maintaining electronic data systems to facilitate data capture and storage across multiple trial sites, site startup and closeout activities, maintaining trial participant records, and assisting with periodic internal site audits for multiple clinical trials.
• Additional duties may include the development and execution of recruiting strategies, management of ClinicalTrials.gov postings, general site coordination and quality control activities, and serving as a resource and mentor for study team members new to the clinical trials research environment.
• Position requires problem-solving and the ability to work independently; participation in regular meetings with researchers; regular and timely coordination of information between patients, clinical, and pre-clinical research teams; and will include providing assistance creating and maintaining constructive collaborations with outside researchers.
Source : CEDENT
