Clinical Research Medical Assistant
About The Position
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, 2025, and 2026! This is a testament to our unwavering commitment to creating an exceptional work environment that fosters growth, collaboration, and employee satisfaction.
Requirements
- Minimum of 1 year of professional experience in a patient-facing healthcare setting
- Self-motivated, energetic, and positive
- Outgoing, personable, and patient-centered approach to every interaction
- Attention to detail
- Warm, professional presence in a fast-paced clinic setting
- Strong judgment, reliability, and follow-through in day-to-day study operations
- Adaptability as site needs evolve and new studies or responsibilities are introduced
- Clear communication with patients, providers, sponsors, and teammates
- Ownership of responsibilities from start to finish
- Ability to move quickly when great candidates and great opportunities are identified
Nice To Haves
- Active RMA, CCMA, CMA, LPN, or RN certificate
- B.S. or B.A. from an accredited university
Responsibilities
- Supporting high-quality clinical trial execution while delivering an excellent experience for patients, physicians, and study partners
- Ensuring patients feel welcomed, informed, and comfortable throughout their study participation
- Completing study visits accurately and efficiently while maintaining strict adherence to protocol requirements
- Supporting patient recruitment, screening, and enrollment activities to help meet study goals
- Prioritizing participant retention so patients attend and complete required visits throughout the trial
- Entering clinical data and visit documentation accurately and in a timely manner across required systems
- Maintaining strong communication with sponsors, CROs, physicians, and internal team members to keep studies moving forward
- Handling sponsor and client interactions professionally to ensure a high level of service both onsite and remotely
- Maintaining physician trust by staying organized, knowledgeable, and proactive in communicating patient and protocol updates
Benefits
- Medical Insurance, with generous employer paid contributions
- Dental and Vision Insurance
- Short and Long Term Disability and Group Life Coverage
- Paid Time Off that builds throughout your career with the company
- 401K (+ discretionary match/profit sharing)
- Quarterly Bonus Plan
- Professional Development Program tailored to each team members profess goals
- Success-Driven Environment
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
