Clinical Research Coordinator
DelRicht Research
20 hours ago
Full-time
On-site
Charleston, South Carolina, United States
$50,000 - $55,000 USD yearly
Registered Nurse
DelRicht Research is seeking a candidate who is excited about patient care and clinical research! This position is ideal for someone who wants to work closely with patients and clinical teams. We’re looking for someone who learns quickly, communicates confidently, and adapts well to change. Candidates with experience in healthcare, patient care, customer service, or other fast-paced professional environments may bring highly transferable skills to this position - no previous research experience is required!
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.
Overall, the Clinical Research Coordinator is responsible for delivering an excellent patient experience while driving accurate, efficient study execution, 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
Patients, physicians, and other stakeholders receive clear, timely communication
Skills Needed to Win
1+ years of professional experience
Strong communication skills, sound judgment, and a decisive, solutions-oriented approach to fast-moving or uncertain situations
High attention to detail and ability to stay organized across competing priorities
Ability to quickly learn protocols, systems, and clinical workflows
A collaborative, patient-focused mindset
Nice-to-have experience includes: Exposure to healthcare, patient care, or clinical trials (nurse , medical assistant, or medical scribe experience is ideal!); comfort with c linical documentation and charting; experience with blood draws, ECGs, and vital signs
Team Perks & Benefits at DelRicht Research
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
Success-Driven Environment where data drives decisions and insights
Job Type : Full-Time, 40+ hrs
Work Schedule : 8am-5pm, Monday through Friday
Location : On-site in Charleston and Mount Pleasant South Carolina
Salary Range : $50,000-$55,000
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.
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.
Overall, the Clinical Research Coordinator is responsible for delivering an excellent patient experience while driving accurate, efficient study execution, 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
Patients, physicians, and other stakeholders receive clear, timely communication
Skills Needed to Win
1+ years of professional experience
Strong communication skills, sound judgment, and a decisive, solutions-oriented approach to fast-moving or uncertain situations
High attention to detail and ability to stay organized across competing priorities
Ability to quickly learn protocols, systems, and clinical workflows
A collaborative, patient-focused mindset
Nice-to-have experience includes: Exposure to healthcare, patient care, or clinical trials (nurse , medical assistant, or medical scribe experience is ideal!); comfort with c linical documentation and charting; experience with blood draws, ECGs, and vital signs
Team Perks & Benefits at DelRicht Research
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
Success-Driven Environment where data drives decisions and insights
Job Type : Full-Time, 40+ hrs
Work Schedule : 8am-5pm, Monday through Friday
Location : On-site in Charleston and Mount Pleasant South Carolina
Salary Range : $50,000-$55,000
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.