Clinical Research Assistant — Oncology Trials

Flourish Research; Crystal River (FL); Sur place; USD 40 000 - 56 000; Plein temps

Avantages offerts par ce poste

Health insurance plans

Dental insurance plans

Vision insurance plans

401(k) with 100% employer match on the

first 4% of employee contributions

Tuition reimbursement

Parental leave

Employee referral program

Employee assistance program

Life insurance

Disability insurance

Generous PTO plan

Résumé du poste

Flourish Research in Crystal River, FL is hiring a Research Assistant to support protocol-driven visits, data collection, and study coordination at our onsite site.

The role requires two years of clinical research experience, familiarity with ICH/GCP, and ability to work with investigators, CRCs, and sponsors; oncology experience is a plus. We offer a comprehensive benefits package and competitive compensation.

Qualifications

• Bachelor's degree preferred, but not required
• Clinical research experience is required, and oncology clinical research experience is preferred
• Minimum of two years of clinical research experience
• Clinical skills: 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.

Responsabilités

• 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

Connaissances

Clinical research

Phlebotomy

EKG/ECG

Communication

Formation

Bachelor's degree preferred

Outils

e-source reporting

Microsoft Office

Description du poste

Flourish Research in Crystal River, FL is hiring a Research Assistant to support protocol-driven visits, data collection, and study coordination at our onsite site.

The role requires two years of clinical research experience, familiarity with ICH/GCP, and ability to work with investigators, CRCs, and sponsors; oncology experience is a plus. We offer a comprehensive benefits package and competitive compensation.