Clinical Administrative Assistant

Posted 2 Days Ago
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Los Angeles, CA, USA
In-Office
26-30 Hourly
Mid level
Healthtech • Biotech • Pharmaceutical
The Role
Provides administrative and operational support to oncology clinical research teams and Principal Investigators. Responsibilities include handling calls and visitors, maintaining records and filing systems, preparing summaries, coordinating meetings and travel, documenting minutes, managing office supplies and equipment maintenance, and tracking expenses and petty cash. Requires three years of clinical administrative experience, strong communication and organizational skills, Microsoft Office proficiency, and a high school diploma or GED.
Summary Generated by Built In

The START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering "Hope Through Access” to cutting edge trials throughout the United States and Europe.   

Position Summary: 

The Clinical Administrative Assistant provides administrative and operational support to oncology research teams, and Principal Investigators. 

The hourly pay rate for this role is $26/hour-$30/hour. However, base pay may vary depending on multiple individualized factors including market location, job-related knowledge, skills, and experience. 


Location: 10700 Santa Monica, Suite 310 Los Angeles, California  90025

Work Schedule: On-Site, 8am-5pm, Monday-Friday

Essential Responsibilities:

  • Answer and transfer phone calls, screening when necessary.
  • Welcome and direct visitors and clients.
  • Maintain filing systems.
  • Retrieve information as requested from records, email, minutes, and other related documents; prepare written summaries of data when needed.
  • Respond to and resolve administrative inquiries and questions.
  • Coordinate and schedule travel, meetings, and appointments for managers or supervisors.
  • Prepare agendas and schedules for meetings.
  • Record and distribute minutes or other records for meetings.
  • Maintain office supplies and coordinate maintenance of office equipment.
  • Maintain a system for recording expenses and the use of petty cash.

Required Education and Experience:

  • High school diploma/GED required.
  • 3 years of experience in a clinical administrative role.
  • Excellent verbal and written communication skills.
  • Excellent interpersonal and customer service skills.
  • Proficient in Microsoft Office Suite or related software.
  • Excellent organizational skills and attention to detail.
  • Basic understanding of clerical procedures and systems such as recordkeeping and filing.
  • Ability to work independently.

Preferred Education and Experience:

  • Associate’s degree.
  • Experience working in a CRO, clinical trial, life sciences, or healthcare environment.

Best-in-Class Benefits and Perks  

We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and 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 coverage and optional insurance options  
  • 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’re committed to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START, you’ll join 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. START represents the world’s largest roster of early-phase principal investigators across its Network of clinical trial sites.

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. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.  

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.  

Skills Required

  • High school diploma or GED
  • Three years of experience in a clinical administrative role
  • Excellent verbal and written communication skills
  • Excellent interpersonal and customer service skills
  • Proficiency in Microsoft Office Suite or related software
  • Excellent organizational skills and attention to detail
  • Basic understanding of clerical procedures and systems, including recordkeeping and filing
  • Ability to work independently
  • Associate's degree
  • Experience working in a CRO, clinical trial, life sciences, or healthcare environment
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The Company
HQ: San Antonio, TX
294 Employees
Year Founded: 2007

What We Do

Deeply rooted in community oncology centers globally, the START Center for Cancer Research ('START') provides patients with access to specialized Phase 1 clinical trials for novel anti-cancer agents. With research sites in the United States and in Spain, Portugal, and Ireland, START’s clinical trial sites have conducted more than 1,500 early phase clinical trials, including for 50 therapies that have gained FDA/EMA approval.

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