Clinical Trials Coordinator
2 weeks ago
The Clinical Research Technician role provides a dynamic work environment with flexible scheduling options within the pharmaceutical research sector. This position is chiefly tasked with overseeing study participants and ensuring that clinical trials are executed, documented, and reported in accordance with established protocols. Each day presents new challenges and opportunities, with hours varying between 0-29 per week based on project needs.
Key Responsibilities- Thoroughly review and comprehend study documentation, timelines, participant requirements, and sponsor expectations.
- Facilitate the check-in and check-out process for study participants while monitoring their adherence to study protocols, safety measures, and any adverse reactions.
- Conduct essential study activities, including recording meal times, taking vital signs, and documenting results accurately.
- Analyze raw data to confirm its precision and reliability.
- Assist in supervising events to guarantee that studies are completed timely and in compliance with Standard Operating Procedures (SOPs) and protocols.
- Ensure the cleanliness and organization of clinical facilities and all areas related to the study.
- Exceptional customer service abilities.
- Strong attention to detail.
- Willingness to work weekends is a plus.
- Flexibility in work hours is essential.
QPS, LLC is committed to providing equal employment opportunities (EEO) to all employees and applicants without regard to race, color, religion, sex, national origin, age, disability, or genetics. In addition to federal law requirements, QPS, LLC adheres to applicable state and local laws governing nondiscrimination in employment in every location where the company operates. This policy encompasses all aspects of employment, including recruitment, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.
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