Clinical Research Coordinator

Flourish Research; Charlotte (NC); Presencial; CAD 73.000 - 106.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Health, dental, and vision insurance

401(k) with 100% employer match

Tuition reimbursement

Parental leave

Employee referral program

Employee assistance program

Life insurance

Disability insurance

Generous PTO

Descripción de la vacante

Flourish Research is hiring a Clinical Research Coordinator to support the Charlotte, NC site. This role involves performing protocol-guided patient visits, phlebotomy, ECGs, and data entry while maintaining strict regulatory compliance and patient confidentiality.

The candidate will ensure accurate CRFs/eCRFs and informed consent processes. The ideal candidate has oncology clinical research experience, at least two years in the field, strong organizational and communication skills, and

Formación

• Bachelor's degree preferred but not required.
• Must have oncology clinical research experience.
• Minimum of two years of clinical research experience.
• Clinical skills: vital signs, EKG/ECG, phlebotomy, injections.
• Familiar with e-source reporting via an electronic platform.
• Clear understanding of ICH, FDA, and GCP regulations.
• Impeccable organizational skills and attention to detail.
• Excellent communication and interpersonal skills.
• Ethical compass, 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.

Responsabilidades

• Execute protocol-specified patient visits and procedures (phlebotomy, IVs, injections, vital signs, ECG/EKG).
• Document assessments and study data per regulations; maintain source documentation; complete CRFs/eCRFs.
• Obtain informed consent per federal regs, GCP, and IRB requirements.
• Ethically recruit qualified subjects to meet enrollment timelines.
• Complete required training; attend investigator meetings; stay current with regulations and Flourish policies.
• Schedule and conduct visits per protocol timelines.
• Protect confidentiality per HIPAA and confidentiality agreements.
• Report adverse events promptly; report SAEs to sponsor within 24 hours and notify PI/Sub-Is.

Conocimientos

Clinical research experience

Phlebotomy

EKG/ECG

Communication skills

ICH/FDA/GCP knowledge

MS Office proficiency

Educación

Bachelor's degree (preferred)

Herramientas

e-source platform

Descripción del empleo

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. WESEEYOU. WE ARE YOU. WE EMBRACE YOU. WE CELEBRATE YOU!

Flourish Research is looking for motivated, talented, creative individuals who want to learn and grow in their careers while contributing to research that changes lives! We offer an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities.

About the Job:

We are actively hiring a Clinical Research Coordinator to supportour Charlottesite. Shift: Monday-Friday regular day shift work hours
Location: Onsite, Charlotte, NC
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.

• 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

Flourish Research offers an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities. Apply today to learn more about how you can join us in our mission to save and improve the lives of others!

• 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 Researchcomplies withthe lawregardingreasonable accommodation for handicapped and disabled employees.