
Clinical Research Coordinator
Required skills
- clinical research experience
- ICH
- FDA
- GCP
- HIPAA
- Informed Consent
- medical terminology
- Microsoft Office Suite
Nice to have
- vital signs
- EKG/ECG
- phlebotomy
- injections
- e-source reporting
- eCRF
Role summary
Flourish Research is seeking a Clinical Research Coordinator for its Mandeville, Louisiana site. This role involves executing protocol-specified patient visits and procedures, documenting study data, obtaining informed consent, recruiting subjects, and reporting adverse events. The ideal candidate will have a minimum of two years of clinical research experience and a strong understanding of ICH, FDA, and GCP regulations. Preferred clinical skills include phlebotomy, IVs, injections, vital signs, and ECG/EKG. Proficiency in e-source reporting and medical terminology is also desired. This is an onsite, non-exempt position with a Monday-Friday work schedule.
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!
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 support our Mandeville, Louisiana site.
Shift: Monday-Friday normal work hours
Location: Onsite, at Mandeville site primarily, but able to work at either NOLA location.
FLSA Classification: Non-Exempt
Compensation: $25-35 per hour (based on experience)
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
Minimum Requirements:
- Bachelor's degree preferred, but not required
- 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.
Similar roles
QC & DATA MANAGEMENT SPECIALISTFlourish Research · Walnut Creek, CA · Onsite
Data Entry ClerkFlourish Research · Century, CA · Onsite- Clinical Research Coordinator II or III (CRC 2-3) PeoriaArizona Liver Health · Peoria, AZ · Onsite
- Clinical Research Coordinator I - Albany, NYIterative Health · Albany, NY · Onsite
Clinical Research Coordinator IITufts Medical Center · Boston, MA · Onsite
Clinical Research CoordinatorShriners Children's · Galveston, TX · Onsite
