Limited Term Clinical Research Coordinator

DelRicht Research • Baton Rouge, LA

5d • $45,000 - $50,000 • Onsite

About The Position

We’re looking for a Limited-Term Clinical Research Coordinator to support our clinical trials. This is a full-time, temporary opportunity for someone who wants to build hands-on clinical research experience while helping a collaborative team manage clinical operations and patient care (no prior clinical research experience required!) You’ll work closely with the existing study team to support daily visits, study activities, and documentation. This role offers a unique opportunity for someone early in their career who is organized, dependable, and motivated to enter the clinical research industry.

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 the past four consecutive years! This is a testament to our unwavering commitment to creating an exceptional work environment that fosters growth, collaboration, and employee satisfaction.

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: Deliver excellent care and a positive experience for our clinical research patients.

Requirements

• Flexibility, positivity, and a team-first approach is necessary in this role.
• Excellent communication, organization, and attention to detail.
• Dependability and the ability to manage multiple responsibilities in a fast-paced environment.
• Prioritize exceptional patient care and contribute to a welcoming, supportive environment
• Balance multiple tasks with focus and efficiency, owning responsibilities from start to finish with accountability
• Stay coachable and eager to learn, as we value growth and team fit even more than years of experience
• Embrace collaboration with a can-do spirit

Nice To Haves

• At least one year of professional work experience in customer service, patient care, or other healthcare environment is preferred.
• A bachelor’s degree is preferred; candidates with relevant hands-on clinical training or experience, including Medical Assistants or LPNs, may also be considered.
• Clinical experience is great, but we also welcome candidates from other industries who demonstrate strong judgment and a willingness to learn.
• Coffee drinkers preferred… tea drinkers accepted :)

Responsibilities

• Support day-to-day study visits and blinded trial activities.
• Assist the study team with uploads, paperwork, and other required documentation.
• Help keep study activities organized and moving efficiently during screening, enrollment, and ongoing participant visits.
• Coordinate closely with team members and respond to changing study priorities.
• Follow study protocols, clinic procedures, and applicable research requirements.
• Take on additional study support tasks as delegated by the team.

Benefits

• 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.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level