Job Description
Job Description
Description
Coordinate day-to-day activities for clinical research studies across various therapeutic areas
Perform direct patient-facing duties, including informed consent, visit scheduling, and follow-up
Manage all aspects of patient recruitment and enrollment across studies, including database reviews, outreach, pre-screening, and communications
Confidently perform blood draws and handle biospecimen processing and shipping in accordance with protocol requirements
Maintain and manage study documentation, source data, and regulatory binders across numerous systems
Support monitoring visits and participate in both internal and external audits
Communicate effectively with sponsors, CROs, investigators, and internal departments
Provide general support to the team and step in across functions as needed to meet study goals
Additional Skills & Qualifications
Required Qualifications:
Minimum 3 years of clinical research coordinator (CRC) experience for industry-sponsored, interventional clinical trials for investigational drugs
Proficiency in patient care, regulatory management, lab specimen handling, monitoring, and auditing
Excellent multitasking, time management, and organizational abilities
Willingness and ability to travel regularly (up to 50%) across sites
Preferred Qualifications:
Fluent in Spanish (spoken and written)
Certified Clinical Research Coordinator (CCRC) certification
Prior experience with multi-site clinical trials or decentralized trial models
Familiarity with clinical trial management systems (CTMS) and electronic regulatory platforms
Flexibility, initiative, and a team-oriented mindset are essential
Candidates must be comfortable working in a fast-paced, high-accountability environment
Pay and Benefits
The pay range for this position is $31.00 - $40.00/hr.
Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:
• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Los Angeles,CA.
Application Deadline
This position is anticipated to close on Oct 3, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.