Limited Term Clinical Research Coordinator

Socket.dev; Charlotte (NC); On-site; USD 52,000 - 64,000; Full time

Job summary

DelRicht Research in Charlotte is seeking a full-time, onsite, Limited Term Clinical Research Coordinator to join our clinic. This position is ideal for someone with professional experience who wants to own patient-facing clinical work, help the clinic run smoothly, and grow toward leadership as the site expands.

You will support study visits, follow protocols, communicate clearly with stakeholders, and ensure patients have an organized, positive experience.

Qualifications

• 3+ years of professional experience in a relevant field.
• Strong communication skills and sound judgment in fast-moving or uncertain situations.
• A decisive, solutions-oriented approach and willingness to step up when needed.
• High attention to detail and ability to stay organized across competing priorities.
• Ability to quickly learn protocols, systems, and clinical workflows.
• Interest in growing into a leadership role over time.

Responsibilities

• Deliver an excellent patient experience while driving accurate, efficient study execution in our Charlotte clinic, ensuring described outcomes.
• Support study visits and follow protocols with clear communication across stakeholders.
• Ensure patients are guided through the study journey to attend and complete required visits.
• Enter clinical and visit data timely and accurately into required systems and documentation platforms.
• Prepare for upcoming study volume, including vaccine-related trials, and coordinate with cross-functional partners.

Skills

Communication skills

Judgment under pressure

Decisive, solutions-oriented

Attention to detail

Fast learner

Leadership potential

Collaboration

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.

About This Role

DelRicht Research is seeking a full-time, onsite, patient-facing Limited Term Clinical Research Coordinator to join our Charlotte clinic. This role is a strong fit for someone with professional experience who is ready for a next step: owning patient-facing clinical research work, helping the clinic run smoothly, and growing toward future leadership opportunities as the site expands.

You’ll work closely with the clinic team to support study visits, follow protocols, communicate clearly across stakeholders, and help ensure patients have an organized, positive experience. We’re looking for someone who can learn quickly, adapt in a changing environment, and step up with confidence when the team needs direction.

This is an opportunity to join a growing clinic with room to take ownership and build a longer-term path into leadership. For someone who may feel capped in their current role, this position offers a path to keep growing without losing the patient-facing aspect of the work.

Please Note: This is a temporary, full-time position slated to last for approximately 12 weeks with the possibility of extension.

Limited Term Clinical Research Coordinator’s Main Objective

Overall, the Limited Term Clinical Research Coordinator is responsible for delivering an excellent patient experience while driving accurate, efficient study execution in our Charlotte clinic, ensuring:

• Patients have a positive, professional, and comfortable experience throughout their time in our clinic


• Patient visits are completed accurately and efficiently, with close adherence to clinical trial protocols and site expectations


• Patient recruitment, screening, and enrollment activities are supported with a strong focus on follow-through


• Patients are guided through the study journey to help ensure they attend and complete required visits


• Clinical and visit data are entered timely and accurately into required systems and documentation platforms


• Upcoming study volume, including vaccine-related trials, is prepared for and executed smoothly


• Internal teammates, patients, and cross-functional partners receive clear, timely communication


• Issues are escalated appropriately, while decisions are handled independently when appropriate


• Daily clinic operations stay organized across competing priorities in a fast-moving environment


• The broader team benefits from strong prioritization, attention to detail, and confident decision-making

Skills Needed to Win

• Required: 3+ years of professional experience in a relevant field


• Strong communication skills and sound judgment in fast-moving or uncertain situations


• A decisive, solutions-oriented approach and willingness to step up when needed


• High attention to detail and ability to stay organized across competing priorities


• Ability to quickly learn protocols, systems, and clinical workflows


• Interest in growing into a leadership role over time


• A collaborative, patient-focused mindset

Nice to Have

• Prior healthcare, clinical research, clinic operations, or patient-facing experience


• Experience in a leadership role, such as charge nurse, team lead, or shift supervisor


• RN, LPN, MA, scribe, urgent care, EDC entry, or other clinical background


• Experience with blood draws, patient visits, or clinical procedures

Job Type: Temporary Full-Time 40+ hrs

We are an equal opportunity employer and consider all qualified applicants equally without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.