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Flourish Research·Metairie, Louisiana
Research Assistant · $21 - $25/hr
Computed from live listings
Shaded band: the middle 50% of 43 posted healthcare roles in Metairie, Louisiana rates. This role sits in the 22nd percentile.
Pay for this role is about 30% below the Metairie, Louisiana median for similar positions.
The Research Assistant will support clinical trial protocols by performing patient procedures such as phlebotomy, vital signs, and EKG/ECG. They are also responsible for maintaining accurate source documentation, managing study supplies, and ensuring compliance with federal and ethical regulations.
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.
We are actively hiring a Research Assistant to support our Metairie, LA site.
Support CRCs and site staff with 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 Obtain and document informed consent following federal regulations and IRB guidelines Support patient recruitment efforts and scheduling to meet enrollment goals Maintain accurate source documentation and complete case report forms (CRFs) Report adverse events to supervisors or investigators as needed Help manage study supplies, lab kits, and other trial materials Maintain confidentiality and follow all applicable compliance and ethical standards Communicate effectively with research team members and document relevant study communications Represent Flourish Research professionally in all interactions Perform additional duties as assigned by management
Market context
In Louisiana, research assistant openings connected to clinical and oncology studies typically seek candidates who can support regulated protocols and patient-facing procedures. Competition may be stronger for applicants with at least two years of clinical research experience, oncology exposure, phlebotomy and EKG skills, and ICH, FDA, and GCP knowledge. Review the original posting carefully; the requirements and benefits here are AI-summarized to save research time, then tailor your application to those priorities.