Clinical Regulatory Coordinator

Job Description

We are seeking a Clinical Regulatory Coordinator to manage, submit, and maintain regulatory documents for IRB and sponsor submissions across multiple studies. This role involves ensuring all study documentation complies with GCP, FDA regulations, and institutional policies.

Responsibilities

• Manage, submit, and maintain regulatory documents for IRB and sponsor submissions across multiple studies.
• Ensure all study documentation complies with GCP, FDA regulations, and institutional policies.
• Maintain regulatory binders and essential study documentation across all active and archived studies.
• Track protocol amendments, safety reports, and correspondence with regulatory bodies.
• Coordinate and support site initiation visits, monitoring visits, audits, and inspections from a regulatory perspective.
• Work collaboratively with clinical and operations staff to ensure timely startup and regulatory readiness.
• Assist in developing SOPs and regulatory workflows to support regulatory operations.
• Provide on-site regulatory support for trial sites during SIVs, monitoring visits, and other ad hoc visits as needed.
  
  

Required Skills

• 4+ years of experience in clinical research regulatory coordination.
• Deep understanding of FDA regulations, GCP, and IRB processes.
• Experience completing internal/external audits.
• Strong organizational skills and attention to detail.
• Ability to manage multiple studies and deadlines simultaneously.
• Excellent written and verbal communication skills.
• Proficient in Microsoft Office and electronic regulatory systems.
• Willingness and ability to travel (up to 25%) across sites.
  
  

Work Environment

This role requires 100% on-site presence with up to 25% travel between sites in LA, Las Vegas, Texas, and DC. Travel planning is provided with a 2-week advance notice.

Pay and Benefits

The pay range for this position is $50000.00 - $85000.00/hr.

Requirements

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 May 2, 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.

Diversity, Equity & Inclusion

At Actalent, Diversity And Inclusion Are a Bridge Towards The Equity And Success Of Our People. DE&I Are Embedded Into Our Culture Through

• Hiring diverse talent
• Maintaining an inclusive environment through persistent self-reflection
• Building a culture of care, engagement, and recognition with clear outcomes
• Ensuring growth opportunities for our people
  
  

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 process due to a disability, please email [email protected] for other accommodation options.