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Clinical Research Supervisor

Actalent

Long Beach, CA · HybridContractSeen 1 day agoSeen in employer's feed 1 day ago

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At a glance

Compensation
No compensation found
Location
Long Beach, CAHybrid
Schedule
Contract
Work Authorization
Not specified

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Requirements

Credentials this posting asks for.

Certified Clinical Research Coordinator (CCRC)ACRP Certification

Job overview

The Clinical Research Supervisor will lead and support personnel conducting Phase I oncology studies, ensuring compliance with GCP and regulatory standards while managing trial execution, resources, and staff development in a hybrid setting at Actalent's Long Beach office.

Skills & qualifications

RequiredNice to have

Skills

Clinical Research SupervisionOncology Clinical ResearchGood Clinical PracticeRegulatory CompliancePhase I Oncology StudiesFirst‑in‑Human TrialsStudy Protocol ManagementData Quality MonitoringTeam CollaborationProcess ImprovementTraining and MentoringPatient Experience Enhancement

Qualifications

Minimum 2 Years Clinical Research Supervisory ExperienceOncology Clinical Research ExperienceCertified Clinical Research Coordinator (CCRC)ACRP CertificationBachelor's Degree in Healthcare or Life Sciences or Related Field

Benefits

Medical Insurance
Dental Insurance
Vision Insurance
401(k) Match
Paid Time Off

Full job description

Clinical Research Supervisor

Required Qualifications

  • Must have a minimum of 2 years of clinical research supervisory/management experience

  • Must have Oncology clinical research experience

  • Thorough understanding of clinical trial regulations, GCP guidelines, and research compliance requirements.

  • Professional certification such as:

  • Certified Clinical Research Coordinator (CCRC)

  • ACRP Certification

  • Bachelor's degree in healthcare, life sciences, or related field, or equivalent combination of education and experience.

Key Responsibilities

  • Supervise and support clinical research personnel involved in Phase I oncology studies.

  • Manage the execution of first-in-human and early-phase oncology clinical trials.

  • Ensure compliance with study protocols, Good Clinical Practice (GCP), institutional policies, and regulatory requirements.

  • Collaborate closely with Principal Investigators, sponsors, research staff, and multidisciplinary clinical teams.

  • Monitor study progress, enrollment goals, data quality, and participant safety.

  • Oversee research operations, workflow efficiency, and resource allocation.

  • Assist in training, mentoring, and performance management of clinical research staff.

  • Facilitate successful study start-up, activation, monitoring visits, and closeout activities.

  • Identify and implement process improvements to enhance research operations and patient experience

Job Type & Location

This is a Contract position based out of Long Beach, CA.

Pay and Benefits

The pay range for this position is $120000.00 - $140000.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

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 hybrid position in Long Beach,CA.

Application Deadline

This position is anticipated to close on Oct 7, 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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

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.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

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