Clinical Research Coordinator - Oncology
Company: Flourish Research
Location: Los Angeles
Posted on: January 6, 2026
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Job Description:
Job Description 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 Clinical Research Coordinators at our
Panorama City site location. This is one of our three oncology
research sites in the Greater Los Angeles area. These locations are
formerly Valkyrie Clinical Trials - we are proud to welcome
Valkyrie Clinical Trials to the Flourish Research network! The
Clinical Research Coordinator assists the Investigators in
executing Phase I, II, III, and IV clinical research trials in
accordance with Standard Operating Procedures (SOPs), FDA and GCP
guidelines, and study protocols while providing an impeccable
patient experience in every, single interaction. Shift:
Monday-Friday, 8:30 AM - 5 PM (occasional weekends) *You will
always have advanced notice for longer shifts, overnights, or
weekends Location: 14850 Roscoe Blvd, Panorama City, CA 91402
Compensation: $72,000 - $79,000 ($34.60 - $37.98/hr) overtime pay
Benefits: Health, dental, and vision insurance plans, 401(k) with
4% match, tuition reimbursement, parental leave, referral program,
employee assistance program, life insurance, disability insurance,
and 15 days of PTO 10 company holidays. RESPONSIBILITIES 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.
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 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! Flourish Research is where clinical trials
thrive. Flourish Research represents one of the industry's most
progressive and diversified clinical trial companies with robust
capabilities in the therapeutic areas of cardiology/metabolic
disorders/renal, CNS, pulmonology, and vaccines. 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 Research is driven by a diverse and inclusive community of
passionate people who are committed to improving the quality of
life of communities around the world. Flourish is committed to a
safe work environment where all employees, customers, and patients
are included, and treated with dignity and respect. Flourish
Research strives to build an organization that attracts and
leverages diversity in our staff, which reflects the diversity of
our local communities. We promote education, acceptance, and
inclusion because there is beauty in diversity. 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! It is the
policy of Flourish Research not to discriminate against any
applicant for employment, or any employee because of age, color,
sex, disability, national origin, race, religion, or veteran
status.
Keywords: Flourish Research, Monterey Park , Clinical Research Coordinator - Oncology, Science, Research & Development , Los Angeles, California