Job Description
Clinical Research Coordinator
Clinical Research Coordinator (CRC) to coordinate day-to-day activities for clinical research studies across various therapeutic areas, including ophthalmology, dermatology, and pulmonology.
- Coordinate daily activities for clinical research studies across multiple therapeutic areas.
- Perform direct patient-facing duties, including informed consent, visit scheduling, and follow-up.
- Manage all aspects of patient recruitment and enrollment, including database reviews, outreach, pre-screening, and communications.
- Confidently perform blood draws and handle biospecimen processing and shipping according to protocol requirements.
- Maintain and manage study documentation, source data, and regulatory binders across various systems, including client's CTMS and sponsor EDC 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.
Qualifications
2 years of Clinical Research experience
Bachelor’s degree
Phlebotomy
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
Background in therapeutic areas such as Ophthalmology, Dermatology, or Pulmonology
Fluent in Spanish (spoken and written)
Pay and Benefits
The pay range for this position is $50000.00 - $85000.00/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 Jun 13, 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 (%20actalentaccommodation@actalentservices.com) for other accommodation options. Actalent
Job Tags
Temporary work,