Clinical Research Coordinator

START Center for Cancer Research; Los Angeles (CA); On-site; USD 59,000 - 73,000; Full time

Benefits offered by this job

401(k) retirement savings plan with a

Annual performance bonus

Generous paid time off

Medical, dental, and vision coverage

Life and disability insurance

Employee Assistance Program

Flexible FSA and HSA plans

Commitment to work-life balance

Collaborative, inclusive culture

Job summary

The START Center for Cancer Research in Los Angeles, CA is seeking a Clinical Research Coordinator to support early phase oncology trials under supervision. The CRC will ensure accurate conduct, data collection, and regulatory compliance according to GCP, with direct patient interaction and data management responsibilities.

This role offers an hourly pay rate of $43–$53 with a Monday–Friday 8:00am–5:00pm schedule and located at 10700 Santa Monica Blvd, Los Angeles, CA 90025.

Qualifications

• High School Diploma or GED required.
• 2 years of clinical research experience.
• Strong attention to detail and accuracy in data collection and documentation.
• Working knowledge of GCP and regulatory requirements.
• Proficient in Microsoft Office Suite and trial management software.

Responsibilities

• Communicate with sponsors, CROs, and staff regarding questions and protocol status.
• Monitor day-to-day conduct of studies to ensure protocol compliance and data integrity.
• Create or review forms to ensure protocol compliance.
• Assist with patient screening and eligibility determination.
• Facilitate the informed consent process and document completion.
• Prepare and manage source documents per procedures.
• Address deviations with leadership to prevent recurrence.
• Assist PI with Serious Adverse Event reports and closeout activities.
• Provide documentation for deviations and SOP-related issues.

Skills

Detail-oriented

Multitasking

Knowledge of GCP

Regulatory compliance

Education

High School Diploma or GED

Tools

Microsoft Office Suite

Clinical trial management software

Job description

The START Center for Cancer Research (“START”) is the world’s largestearly phasesite network, fully dedicated tooncologyclinical research.Throughout ourhistory, START has provided hope to cancer patients inglobalcommunity practices by offering“Hope Through Access”tocutting edgetrials throughout the UnitedStatesand Europe.

We are currently hiring a Clinical Research Coordinator. The Clinical Research Coordinator (CRC) will work under the guidance of senior research staff to support the daily activities of early phase oncology clinical trials. The CRC ensures the accurate and timely conduct of clinical research, adhering to protocols, regulatory requirements, and patient safety standards. This role involves direct patient interaction, data collection, and maintaining compliance with Good Clinical Practice (GCP).

The hourly pay rate for this role is$43/hour-$53/hour. However, base pay may vary depending on multiple individualized factors including market location, job-related knowledge, skills, and experience.

Work Schedule:Monday-Friday 8:00am-5:00pm

Location: 10700 Santa Monica,Los Angeles, California90025

Essential Responsibilities:

• Communicate on a regular basis with Study Sponsor’s, CRO’s, staff, etc. regarding questions, concerns, as well as status of the protocol.
• Monitor the overall day-to-day conduct of assigned studies in accordance with the specified protocol requirements, Standard Operating Procedures, and Good Clinical Practice to ensure integrity regarding all aspects of the study.
• Create/review forms created or revised for assigned trials to assure protocol compliance.
• Assist with patient screening and determination of eligibility.
• Facilitate the informed consent process ensuring that consent is appropriately completed.
• Prepare and manage source documents according to standard operating procedures.
• Recognize deviations to the protocol and will work with leadership and staff to address corrective actions to prevent deviations.
  
• Work with the Principal Investigator to complete and submit Serious Adverse Event reports.
• Perform protocol specific closeout related activities in conjunction with the data coordinator.
• Provide documentation for all deviations whether related to the protocol or a SOP.
  

Required Education and Experience:

• High School Diploma or GED.
• 2 years of clinical research experience.
• Basic understanding of oncology clinical trials, particularly Phase 1 studies.
• Strong attention to detail and accuracy in data collection and documentation.
• Ability to manage multiple tasks and meet deadlines in a fast-paced environment.
• Working knowledge of GCP and regulatory requirements.
• Proficient in Microsoft Office Suite and clinical trial management software.

Preferred Education and Experience:

• Experience workingin an oncology setting.

Best-in-Class Benefits and Perks

We value the time, talent, and dedication our employees bring to START. Our commitment to yourwell-beingand growth is reflected in a competitive compensation package—based on experience—along with comprehensive benefits designed to support you both personally and professionally:

• 401(k) retirement savings plan with employer match

• Eligibility for an annual performance bonus, based on role and company results

• Generous paid time off and paid holidays

• Comprehensive medical, dental, and vision coverageand optional insuranceoptions

• Company paid life and disability insurance for added financial protection

• Employee Assistance Program (EAP) providing confidential, no‑cost support for you and your family from day one

• Flexible FSA and HSA plans to support your financial wellness

• Commitment to a supportive environment that values balance, wellbeing, and flexibility

• We’recommitted to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START,you’lljoin a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation.

More About START

START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. STARTrepresentsthe world’s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of “Hope Through Access”.As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda –one ofthe most effective cancerdrugsin medical history.

Learn more at STARTresearch.com.

Ready to be part of a team changing the future of cancer treatment?

Join us in our mission to conquer cancer, one clinical trial at a time. Yourexpertiseand dedication can help us bring hope and healing to patients worldwide.

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.