Clinical Research Coordinator

Flourishresearch; Murrieta (CA); On-site; USD 42,705 - 52,348; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

401(k) with 100% employer match on the

first 4% of employee contributions

Tuition reimbursement

Parental leave

Referral program

Employee assistance program

Life insurance

Disability insurance

PTO + holidays

Job summary

Flourish Research seeks an experienced clinical research professional for oncology trials in Murrieta, CA. The role involves coordinating protocol visits, documenting data, and ensuring regulatory compliance.

You will conduct patient visits, obtain consent, recruit subjects, and maintain study materials while collaborating with PIs, teams, and sponsors in a compliant, ethical manner.

Qualifications

• 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.
• Excellent communication and interpersonal skills with PI, team, sponsors, and subjects.
• Ethical compass and attention to detail.

Responsibilities

• Execute protocol-specified patient visits and procedures.
• Document assessments and study data per regs/GCP; complete CRFs/eCRFs.
• Obtain informed consent per federal regs, GCP, and IRB requirements.
• Ethically recruit qualified subjects to meet enrollment timelines.
• Attend investigator meetings and training; stay current with Flourish policies.
• Schedule and conduct visits per protocol timelines.
• Maintain confidentiality per HIPAA and agreements.
• Report adverse events to sponsor and PI as required.
• Manage study materials and communications with study team.

Skills

Oncology clinical research experience

Clinical research experience (2+ years

e-source reporting

ICH FDA GCP regulations

Excellent communication

Medical terminology knowledge

Microsoft Office proficiency

Education

Bachelor's degree preferred

Tools

Microsoft Office Suite

Job description

Overview

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

Position Details

Shift: Monday-Friday, 8:30 AM – 5:00 PM (occasional weekends)
Location: 25405 Hancock Ave, Suite 110, Murrieta, CA 92562
Compensation: $31.00–$38.00/hr depending on experience

Responsibilities

• Execute protocol-specified patient visits and procedures, which may include 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 and 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.

Qualifications

• 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.
• 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.
• Ethical compass that compels honesty, detail‑orientation, and self‑drive.
• 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; referral program; employee assistance program; life insurance; disability insurance; 15 days of PTO + 8 paid holidays and 2 floating holidays.

Equal Employment Opportunity Statement

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.