Clinical Research Coordinator

Flourish Research; Jacksonville (FL); On-site; USD 52,000 - 64,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

401(k) with employer match

Tuition reimbursement

Parental leave

Employee referral program

Employee assistance program

Life insurance

Disability insurance

Paid holidays

Job summary

Flourish Research is hiring a Clinical Research Coordinator for our Jacksonville, FL site. The role focuses on executing protocol visits, data documentation, and informed consent per GCP and IRB standards.

Ideal candidates have oncology clinical research experience, strong organizational and communication skills, and are comfortable handling study materials and regulatory requirements. Onsite role with regular hours, comprehensive benefits, and a team-driven environment.

Qualifications

• Minimum of two years of clinical research experience.
• Oncology clinical research experience preferred.
• Bachelor's degree preferred, but not required.
• Familiar with e-source reporting via an electronic platform.
• Strong knowledge of ICH, FDA, and GCP regulations.
• Excellent communication and interpersonal skills.
• Impeccable organizational skills and attention to detail.
• Proficiency with Microsoft Office Suite.

Responsibilities

• Execute protocol-specified patient visits and procedures, including phlebotomy, IVs, injections, vital signs, ECG/EKG.
• Document assessments and study data per regs/GCP; maintain source; complete CRFs/eCRFs.
• Obtain informed consent per federal regs, GCP, and IRB requirements.
• Ethically recruit qualified subjects to meet enrollment timelines.
• Schedule and conduct visits per protocol timelines.
• Protect confidentiality per HIPAA and all confidentiality agreements.
• Report AEs promptly; report SAEs to sponsor within 24 hours and notify PI/Sub-Is.
• Maintain documentation of communication with Leads, Managers, PIs/Sub-Is, and study team.

Skills

Oncology clinical research experience

Excellent communication

Organizational skills

Attention to detail

Critical thinking

HIPAA knowledge

Proficiency with MS Office

Education

Bachelor's degree

Tools

Microsoft Office Suite

Job description

About Us

Flourish Research is where clinical trials thrive. Flourish Research is one of the industry's most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research. At Flourish Research, we strive toward excellence. In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of their race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation, or veteran status. We embrace employees, customers, and patients from these underrepresented groups to help make this vision a reality. Flourish is committed to a safe work environment where all employees, customers, and patients are included, and treated with dignity and respect. The more diversity we have in our team, the more unique perspectives, and ideas we share, and the better prepared we are to serve our communities. WE SEE YOU. WE ARE YOU. WE EMBRACE YOU. WE CELEBRATE YOU.

About the Job

We are actively hiring a Clinical Research Coordinator to support our Jacksonville, FL site.

Shift: Monday-Friday normal work hours

Location: Onsite

FLSA Classification: Non-Exempt

ESSENTIAL JOB FUNCTIONS

• Execute protocol-specified patient visits and procedures, which may include, but not limited to, phlebotomy, IVs, injections, vital signs, ECG/EKG, etc.
• Document assessments and study data per regs/GCP; maintain complete source; accurately complete CRFs/eCRFs.
• Obtain informed consent per federal regs, GCP, and IRB requirements.
• Ethically recruit qualified subjects to meet enrollment timelines.
• Complete required/ongoing training; attend investigator meetings/courses; stay current with changing regulations and Flourish policies.
• Schedule and conduct visits per protocol timelines.
• Protect confidentiality per HIPAA and all confidentiality agreements.
• Report AEs promptly; report SAEs to sponsor within 24 hours and notify PI/Sub-I/supervisor.
• Account for and ensure availability of trial materials (study drug, labs, CRFs, supplies).
• Maintain and document communication with Leads, Managers, PIs/Sub-Is, and study team per protocol and policy.
• Perform duties safely, and in a time-/cost-effective manner compliant with Flourish policies.
• Represent Flourish professionally in all interactions.
• Additional duties as assigned by management.

Requirements

• Bachelor's degree preferred, but not required.
• Must have oncology clinical research experience.
• Minimum of two years of clinical research experience.
• Clinical skills highly preferred: vital signs, EKG/ECG, phlebotomy, and injections.
• Familiar with e-source reporting via an electronic platform.
• A clear understanding of ICH, FDA, and GCP regulations.
• Impeccable organizational skills and attention to detail.
• Excellent communication and interpersonal skills to effectively interact with the Principal Investigator, research team, Study Sponsor/CROs, potential subjects, and referral sources.
• An ethical compass that compels the candidate to be honest, detail-oriented, and self-driven.
• High-level critical thinking skills.
• Working knowledge of medical terminology and lab collection/processing/storage procedures.
• Proficiency with computers and Microsoft Office Suite.

Benefits

Health, dental, and vision insurance plans, 401(k) with a 100% employer match on the first 4% of employee contributions, tuition reimbursement, parental leave, employee referral program, employee assistance program, life insurance, disability insurance, and a generous PTO plan covering vacation, sick, personal days and 8 paid holidays.

Flourish Research is an equal employment opportunity employer. Employment decisions are based on merit and business needs, and not on race, color, sex, (including pregnancy and gender identity), citizenship status, national origin, ancestry, gender, sexual orientation, age, religion, creed, physical or mental disability, genetic information, marital status, veteran status, political affiliation, or any other factor protected by law. Flourish Research complies with the law regarding reasonable accommodation for handicapped and disabled employees.