CenExel
Location
Cherry Hills Village, Colorado
Salary
$28 - $35 / HOUR
The role is responsible for assisting in coordinating all aspects of clinical trials from initiation to completion, ensuring strict adherence to ICH, GCP, protocol, and company guidelines. Duties include organizing research information, observing subjects, scheduling data collection, documenting adverse events, and performing safety/efficacy assessments per protocol.
Candidates must have a high school diploma or equivalent, with a Bachelor's degree preferred, and 0-3 years of experience in the medical field. Essential skills include knowledge of federal regulations protecting human subjects, strong leadership, problem-solving abilities, and effective verbal and written communication.
$27.93-$35.00/hour (Depending on education, experience, and skillset)
Responsible for assisting with coordinating clinical trials with the strictest adherence to ICH (International Conference on Harmonization), GCP (Good Clinical Practices), protocol, and company guidelines, regulations, and policies.
CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.
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