Clinical Screening Coordinator

Centricity Research; Rincon (GA); On-site; USD 28,929 - 31,684; Full time

Benefits offered by this job

Health insurance

Dental & Vision

Flexible PTO

Education reimbursement

401(k) with match

Job summary

Centricity Research Rincon, Georgia, United States is seeking a Clinical Screening Coordinator to lead recruitment initiatives and enroll high-quality patients per study protocols.

This fully on-site role offers an hourly rate with incentive compensation. You’ll screen patients, manage recruitment data, and engage with communities to promote clinical trials at Centricity Research.

Experience in healthcare or customer-facing roles is welcome; CTMS/EMR familiarity is a plus.

Qualifications

• Communication with patients in phone, email, and in person.
• Organized and detail-oriented with ability to manage multiple tasks.

Responsibilities

• Lead enrollment and retention initiatives and screen patients for eligibility.
• Maintain recruitment tracking logs and data queries in CTMS/EMR systems.
• Attend community events to promote Centricity Research and recruit participants.
• Complete informed consent and screening visits per study protocol.

Skills

Communication with patients

Organization & detail-oriented

CTMS/EMR familiarity

Healthcare/customer-facing experience

Job description

Clinical Screening Coordinator

Centricity Research Rincon, Georgia, United States

About this position

Join Us at Centricity Research!

Centricity Research is one of the largest clinical research networks in North America. We area fully centralized Integrated Research Organization (IRO) specializing in conducting Phase I-IV clinical trials in over 35 therapeutic areas: inpatient and outpatient; pharmaceutical, biotechnology, and medical device trials.

About the Role

We’relooking for a Clinical Screening Coordinator to lead research-related recruitment initiatives and ensure the enrollment of high-quality patientsin accordance withCentricity Research recruitment guidelines. In this role,you’llalsoscreen patients for participation in clinical research studies with a solid understanding of study protocols, including inclusion/exclusion criteria, relevant medications, and medical conditions.

This is a fully on-site role. In addition to the hourly rate, this role is eligible for incentive compensation.

What You’ll Do

Work on enrollment and retention initiatives withthe Site Manager Problem solve and create contingency plans tooptimizeenrollment via recruitment initiatives Obtain andmaintaincomputerizeddatabaseof all ad callers Return all phone calls/email responses to interested patients within 24 -48 hours Accurately complete recruitment tracking log and all applicable clinical trial management systems Identifyappropriate studycandidacy based on knowledgeofsites’recruiting and upcoming studies Complete database query reviews for study candidacy and conduct outbound calls for study interest Provide study metrics on a regular basis and provide ongoing feedbackregardingoutcome of recruitment initiatives Occasionally attend community lectures, healthfairsor events to promote Centricity Research Promote clinical trials in the community through outreach events Complete Informed Consent and screening visits per study protocol and Centricity Research SOP Perform delegated tasks completely and accurately, including review of demographic information, medication history, medical history, obtaining vital signs(blood pressure, heart rate, temperature, and waist, weight, and height measurementsComplete the source documents, case report forms, and data queriesin a timely manner, accurately, and completely. Assist theCentral Recruitment, Research Operations and/or Investigators with any other tasks asrequired Able to work in a regional setting to support sites with recruitment and screening as needed

You Might Be a Great Fit If You:

• Communicate clearly and comfortably with patients by phone, email, and in person
• Stay organized and pay attention to details, especially when managing multiple tasks like outreach, documentation, and scheduling
• Arecurious about clinical research and excited to learn protocols, medical terminology, and research ethics
• Feelconfident using everyday computer tools like spreadsheets, databases, and email,and are open to learning systems like CTMS or EMR
• Bring experience from a healthcare, research, or customer-facing role,or are ready to dive in and learn on the job

Why Centricity Research?

Our Mission

We connect people to scientific advancements through groundbreaking research within a deeply human experience.

Our Core Values

• Quality: We aim for excellence and integrity in everything we do - because lives depend on it.
• Care: We show up for each other, our customers, and our mission - always going the extra mile.
• Be the Change You Seek: We'readaptable, forward-thinking, and constantly improving - for the betterment of all.
• One Team: We collaborate, support one another, and succeed together.
• Grow for Good: We grow with purpose - to expand access to research and improve global health.
• Own It: We take initiative, deliver results, and follow through - with passion and accountability.

Benefits

• Comprehensive health, dental, and vision insurance
• Enhanced EAP – mental health support
• Flexible PTO + paid holidays
• Continuing education reimbursement
• 401(k) / RRSP with company match and immediate vesting

We’rean equal opportunity employer committed to building a diverse and inclusive workplace. We welcome applicants from all backgrounds and will provideaccommodationsduring the hiring process upon request.

The pay range for this role is:

21.00-23.00USD per hour (Centricity Research Rincon Pulmonology)