ProTrials Research Inc.
CRO management services • Clinical Monitoring • Clinical Project Management • Clinical Site Management • Clinical Study Start-up
51 - 200
Senior Clinical Research Associate
October 1
ProTrials Research Inc.
CRO management services • Clinical Monitoring • Clinical Project Management • Clinical Site Management • Clinical Study Start-up
51 - 200
Description
• We opened our doors with a clear and simple vision: to provide the worldwide clinical research industry with professional services that demonstrate the highest level of experience, quality, and integrity. • Since 1996, ProTrials has supported research that has led to ground-breaking treatments and solutions in the pharmaceutical, biotechnology, and medical device industries. • Most of us entered the clinical research field to help patients, caregivers, or maybe even our loved ones. • We show up every day committed to do work that matters. • When you join ProTrials, you will join a collaborative community helping to build a healthier world. • We also understand your need to balance a meaningful workload with life’s every-day moments. • At ProTrials, we know that this makes our employees happier, healthier, and more successful. • The Senior Clinical Research Associate (Sr. CRA) plays an integral part in the successful monitoring and management of clinical trials. • Responsibilities of a Sr. CRA include ensuring clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH GCP, and all applicable regulatory requirements. • Sr. CRAs may be required to travel up to 65%.
Requirements
• RN or Bachelor and/or advanced degree in biological sciences or related field, or equivalent combination of relevant experience, education or training, and previous CRA experience demonstrating career growth in the CRA position • Detail-oriented • Excellent organizational skills, strong interpersonal and communications skills, and strong problem-solving skills • Flexibility with changing priorities • Ability to efficiently perform and prioritize multiple tasks • Familiarity with the medical and pharmaceutical industries, and related terminology and practices • Extensive knowledge of FDA regulations and their practical implementation • Ability to travel, including by air or by car on short notice • Computer proficiency in Microsoft Word, Excel, and PowerPoint
Benefits
• Competitive pay • Career growth • Full medical, dental, and vision benefit packages • 401(k) with match • Commuter benefits • Legal benefits • The best coworkers, if we do say so ourselves
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