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.

The Healthcare Project Coordinator is a strategic project management role, ensuring a successful start to clinical research trials across our site network. This role is ideal for a candidate who is excited to learn from the ground up, take ownership of their work, and contribute to both the patient experience and the operational success of clinical trials. We are looking for someone who can thrive in a busy clinic setting, support a high volume of activity, and help the team expand capacity as new studies begin.

The right candidate will be comfortable in an onsite, patient facing role.

Requirements

are completed accurately Site capacity is strengthened by helping the team manage a high volume of patient visits and related study activity Communication with sites across the country is clear, professional, and responsive as study needs evolve Deadlines, competing priorities, and ad hoc requests are managed effectively across multiple active studies Sponsors, CROs, and internal stakeholders receive consistent communication and dependable follow-through throughout the start-up process Systems-based and technical tasks, including research-related build or configuration work, are completed carefully and efficiently Clinical teams are equipped with accurate materials, summaries, and operational support needed to launch studies successfully Skills needed to win Required : Bachelor’s degree from an accredited university. Required : 1+ year of professional experience Required : Strong organization, communication, and time management skills in healthcare, clinical research, project coordination, administrative operations, vendor coordination, or systems-related work This is an onsite Monday-Friday position. Priority will be given to local candidates.

Comfort with medical terminology, electronic medical record systems, written communication, and learning technical computer systems is important for success in this role. The Right Candidate Will Be self motivated! Energetic!

Positive!

Responsibilities

Communicate clearly and professionally in both verbal and written formats with internal teams and external partners Be highly adaptable when deadlines shift, priorities change, or urgent requests arise Troubleshoot independently and think proactively about next steps instead of wait