CRO management services • Clinical Monitoring • Clinical Project Management • Clinical Site Management • Clinical Study Start-up
October 1
CRO management services • Clinical Monitoring • Clinical Project Management • Clinical Site Management • Clinical Study Start-up
• 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%.
• 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
• 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
Apply NowSeptember 20
Clinical Research Associate coordinating monitoring for clinical trials at Thermo Fisher Scientific.
September 16
Monitor clinical trials and ensure compliance at investigative sites for Orca Bio.
September 16
501 - 1000
Site monitor ensuring data quality and patient safety for BeiGene's clinical studies.
September 15
Clinical Research Associate for cancer patient drug development at Immatics.
September 15
Immatics seeks a Clinical Research Associate to oversee clinical trial monitoring.