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 in 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.

Lead Clinical Research Coordinator’s Main Objective: Overall, the Lead Clinical Research Coordinator is responsible for providing quality, excellent patient care and a great experience for our patients in our clinical research studies:

• Lead by example in delivering warm, excellent care to every patient at every visit.
• Ensure patient visits are conducted with 100% protocol adherence—accurately, efficiently, and on time.
• Perform and self-review clinical charting with a focus on accuracy, compliance, and quality.
• Prepare, administer, and document investigational products and medications per study protocols.
• Collect and enter clinical data, including patient questionnaires, into multiple online systems.
• Communicate clearly and professionally with pharmaceutical sponsors, physicians, and your team.
• Serve as a trusted, knowledgeable liaison for physicians—keeping them updated on their schedules, patient statuses, and protocol requirements.
• Support, guide, and coach Clinical Research Coordinators to maintain high standards of patient care and operational excellence.
• Act as the Site Manager’s delegate in their absence, ensuring clinic operations continue smoothly.

SKILLS NEEDED TO WIN:

• Required: 3-4 years of professional experience in a Healthcare setting
• Required: Patient facing experience
• Required: Strong communication and decision-making skills
• This is an onsite Monday-Friday position.
• Coffee drinkers preferred. Tea drinkers accepted.

• Lead by example in delivering warm, excellent care to every patient at every visit.
• Ensure patient visits are conducted with 100% protocol adherence—accurately, efficiently, and on time.
• Perform and self-review clinical charting with a focus on accuracy, compliance, and quality.
• Prepare, administer, and document investigational products and medications per study protocols.
• Collect and enter clinical data, including patient questionnaires, into multiple online systems.
• Communicate clearly and professionally with pharmaceutical sponsors, physicians, and your team.
• Serve as a trusted, knowledgeable liaison for physicians—keeping them updated on their schedules, patient statuses, and protocol requirements.
• Support, guide, and coach Clinical Research Coordinators to maintain high standards of patient care and operational excellence.
• Act as the Site Manager’s delegate in their absence, ensuring clinic operations continue smoothly