Clinical Research Coordinator

Moffitt

. Screen, recruit, and enroll research participants .

Posted 11/12/2026full-timeFlorida • United StatesJuniorMid-Level💰 $26 - $40 per hourWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in clinical trials coordination, including participant recruitment, protocol compliance, and documentation management. Possesses strong organizational and communication skills to effectively liaise between patients, clinical teams, and sponsors.

Highest-signal resume keywords

Clinical Trials Coordination ExperiencePatient Recruitment and EnrollmentStrong Written and Verbal Communication SkillsCCRP or CCRC CertificationKnowledge of Clinical Research Processes

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Data EntryResearch Documentation ManagementProtocol ComplianceClinical Trial ProceduresPatient Care Coordination

Soft Skills

Organizational SkillsInterpersonal SkillsMentoring Abilities

Certifications & Qualifications

CCRPCCRC

Industry Keywords

Clinical ResearchGood Clinical PracticeClinical TrialsResearch ProtocolsBiotechnologyPharmaceutical Organizations

About the role

Key responsibilities & impact

Screen, recruit, and enroll research participants
Educate patients and families about clinical trials
Coordinate research patient care
Facilitate research visits and procedures
Support safety and protocol compliance
Maintain accurate research documentation
Coordinate across multiple clinical and research teams
Serve as a connection between patients, investigators, clinical care teams, sponsors, regulatory professionals, data teams, and other departments
Translate complex research protocols into safe, coordinated patient experiences
Coordinate research visits and protocol-required activities from screening and enrollment through treatment and follow-up
Work with study sponsors ranging from emerging biotechnology companies to leading pharmaceutical organizations
Identify concerns and escalate issues for clinical or investigator input
Progressively take on complex trials and patient populations, work with greater independence, mentor coordinators, contribute to process improvement, and serve as subject matter experts

Requirements

What you’ll need

Bachelor's degree required for Clinical Trials Screening Coordinator
Two years of experience in clinical trials for Clinical Trials Screening Coordinator
Associate degree required for Associate Clinical Research Coordinator
In lieu of an associate degree, two years of relevant experience with a high school diploma or GED
Experience with data entry and strong written, verbal, and organizational skills
Clinical Research Coordinator I: bachelor's degree with one year of relevant clinical, health-related, scientific, business, or research experience
In lieu of a bachelor's degree, an associate degree with an additional year of relevant experience, for a total of two years of experience
Clinical Research Coordinator II: bachelor's degree with two years of clinical trials coordination experience
In lieu of a bachelor's degree, an associate degree with four years of clinical trials coordination experience may be considered
CCRP, CCRC, or equivalent certification preferred for Clinical Research Coordinator II
Clinical Research Coordinator III: bachelor's degree with four years of clinical trials coordination experience
In lieu of a bachelor's degree, an associate degree with six years of clinical trials coordination experience may be considered
CCRP or CCRC certification required for Clinical Research Coordinator III
Senior Clinical Research Coordinator: bachelor's degree with six years of clinical trial coordination experience
In lieu of a bachelor's degree, an associate degree with an additional two years of clinical trial coordination experience, for a total of eight years, may be considered
CCRP or CCRC certification required for Senior Clinical Research Coordinator
Knowledge of clinical research processes, procedures, and protocols
Excited to learn clinical research regulations, study protocols, and Good Clinical Practice requirements
Ability to work Monday through Friday
Hybrid work arrangement after successful completion of the 90-day introductory and training period

Benefits

Comp & perks

Hybrid work opportunity combining on-site and remote work following successful completion of the 90-day introductory and training period
Training and orientation through the Human Subject Research (HSR) Academy and Clinical Trials Office (CTO)
Relocation assistance may be available