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DelRicht Research
Clinical Research Medical Assistant
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What they do
A Clinical Research Associate is responsible for running clinical trials, usually for an organization undertaking pharmacological drug testing. Will ensure that trials adhere to good clinical practice guidelines for monitoring clinical trials.
$100,132 / year median in Oklahoma
-1% projected decline
Job Description
Why DelRicht Research? Would you love to be a part of the cutting edge of healthcare and science innovation? Do you want to be an influential part of a rapidly growing team? Are you looking for a position that has sustainable opportunity for professional growth? If the answer is yes, then DelRicht Research might be the right opportunity for you! Who We Are DelRicht is a clinical research company dedicated to providing an excellent customer experience to all patients that participate in our clinical trials. Our clinical trials provide new treatment options for our patients and ultimately our goal is to get new medications and medical devices FDA approved! We hold our team members to a high standard of excellence and are looking for energetic, positive, quick learners to be a part of our team. Presently our network stretches across 33 sites throughout the United States in 18 states. DelRicht Research has been recognized as a Top Workplace for 2023, 2024, and 2025! This is a testament to our unwavering commitment to creating an exceptional work environment that fosters growth, collaboration, and employee satisfaction. Clinical Research Medical Assistant's Main Objective Overall, the Clinical Research Medical Assistant is responsible for supporting high-quality clinical trial execution while delivering an excellent experience for patients, physicians, and study partners: Patients feel welcomed, informed, and comfortable throughout their study participation Study visits are completed accurately and efficiently while maintaining strict adherence to protocol requirements Patient recruitment, screening, and enrollment activities are supported to help meet study goals Participant retention is prioritized so patients attend and complete required visits throughout the trial Clinical data and visit documentation are entered accurately and in a timely manner across required systems IM injections are administered safely and accurately Strong communication is maintained with sponsors, CROs, physicians, and internal team members to keep studies moving forward Sponsor and client interactions are handled professionally to ensure a high level of service both onsite and remotely Physician trust is maintained by staying organized, knowledgeable, and proactive in communicating patient and protocol updates Skills needed to win