Research Assistant

Posted 7 Days Ago
Be an Early Applicant
Panorama Heights, CA
In-Office
23-33 Hourly
Junior
Biotech
The Role
Assist in clinical research protocols, support patient interactions, document assessments, and maintain study records under supervision.
Summary Generated by Built In

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 Research Assistants 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 Research Assistant is to assist under the direct supervision of the Site Director or Clinical Research Coordinator (CRC) in clinic supporting activities and perform duties and procedures related to the start-up, conduct, and close-out phases of clinical research protocols while providing an impeccable patient experience in every single interaction.
Shift:  Monday-Friday, 8:30 AM - 5 PM (occasional weekends)
Location:  14850 Roscoe Blvd, Panorama City, CA 91402
Compensation:  $23-$33/hr - depending on experience
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

  • Professionally represent Flourish Research in all interactions with patients, sponsors, and clinical partners.
  • Review study protocols and support protocol-specific patient visits and procedures.
  • After training, accurately document patient assessments, observations, and test results per protocol and regulations.
  • Obtain and document informed consent in accordance with federal, IRB, and GCP requirements.
  • Help recruit, screen, schedule, and follow up with study subjects to meet enrollment and visit timelines.
  • Maintain complete and accurate source documents, CRFs/eCRFs, and other study records.
  • Protect patient and study confidentiality and promptly report adverse events to appropriate team members.
  • Assist with investigational product and study supply accountability and documentation.
  • Communicate regularly with the Team Lead, CRCs, Site Director, PI, and study team and document as required.
  • Participate in required training, stay current on regulations, and perform duties safely, efficiently, and as assigned.
  • Other duties as assigned by leadership
QUALIFICATIONS
  • Associate's degree in Science or equivalent clinical research experience; Bachelor’s degree preferred.
  • 1–3+ years of experience in clinical or biological research.
  • ECG, phlebotomy, and other protocol-related technical skills preferred.
  • Solid understanding of clinical research methods and GCP/regulatory concepts.
  • Strong oral and written communication skills; able to collaborate across research teams.
  • Proficient with Office 365 and general computer applications.
  • Demonstrates professionalism, strong work ethic, integrity, and attention to detail.
  • Adaptable team player who can take on additional tasks, support process improvements, and help train new hires.

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.

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The Company
HQ: Apex, North Carolina
458 Employees

What We Do

Flourish Research is a fully integrated clinical trial organization in North America. We acquire and operate large, best-in-class sites with the very best medical and scientific expertise, meaningful diversity, and reliable recruitment.

The Flourish Difference:

Meaningful Diversity - We constantly innovate our approach to support diversity in our patient populations and employees.

Exceptional Scale and Agility - By acquiring and operating some of the largest and best-in-class research sites, we give you the simplified tools to scale when study requirements shift.

Shared Tech Platforms and Processes - Your patient information is vital – that’s why our sites use unified platforms and give you 24/7 monitoring and e-access to all patient data.

Pioneering Thought Leadership - Our leading investigators are dedicated to research and your studies.

Focused Therapeutic Expertise - Our team leverages its depth of expertise in core therapeutic areas.

Early Phase Capabilities - Access is everything. To help with study requirements, we operate early-phase inpatient units with unparalleled access to healthy and diseased patient populations.

Integrated Systems - The convergence of quality, training and site standards across all sites ensures defined support for your studies.

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