Senior Clinical Research Coordinator

As a Senior Clinical Research Coordinator, you will play a pivotal role in managing and coordinating clinical trials. You will be responsible for study coordination, including study start-up, patient recruitment, and providing backup support. You will ensure that all aspects of the trial are managed efficiently and effectively, adhering to timelines and regulatory requirements.

Responsibilities

+ Serve as the primary contact to ensure appropriate communications, trial management, and meeting of timelines.

+ Coordinate the operational aspects of new and ongoing clinical trials at the site.

+ Work under the supervision of the Principal Investigator(s), exercising excellent clinical judgment in patient monitoring and care.

+ Maintain daily contact with the Principal Investigator(s) for recruitment activities, study start-up, and general daily communication.

+ Execute the protocol and ensure that all staff working on any given protocol have been properly delegated by the Principal Investigator and adequately trained.

+ Recruit and pre-screen patients.

+ Maintain and submit IRB communications and regulatory documents.

+ Communicate timely with internal teams, investigators, review boards, and study subjects.

+ Prepare study materials as requested by the Principal Investigator, such as informed consent documents, case report forms, enrollment logs, and drug/device accountability logs.

+ Perform other duties as assigned.

Essential Skills

+ Patient recruitment

+ Clinical trial management

+ Clinical research

+ Good Clinical Practice (GCP)

+ Oncology

+ Phlebotomy

Additional

Skills & Qualifications

+ At least a High School Diploma

+ Prior Clinical Research Coordinator experience (3+ years)

+ Oncology experience

Work Environment

The position requires on-site work five days a week in a patient-facing clinic environment.

Job Type & Location

This is a Contract position based out of Los Alamitos, CA.

Pay and Benefits

The pay range for this position is $30.00 - $42.00/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 Alamitos,CA.

Final date to receive applications

This position is anticipated to close on Jan 19, 2026.

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 actalentaccom (%20actalentaccom)  for other accommodation options.