Clinical Research Coordinator-oncology

Actalent

Merced, CAFull-time

Behavioral Health Market Context

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Benefits

Dental CoveragePaid Time OffHealth Insurance

Job Description

imary point of contact for sponsors (excluding budget and contracting)Conduct informed consent discussions with patientsCoordinate scheduling for standard-of-care proceduresEnsure accountability and compliance for Investigational Products (IP)Collaborate with nursing staff for blood draw coordinationMaintain direct communication with Principal Investigators and actively manage PI engagementPay and BenefitsThe pay range for this position is $35.00 - $39.00/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 TypeThis is a fully onsite position in Merced,CA.Application DeadlineThis position is anticipated to close on Aug 22, 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 [email protected] for other accommodation options.

Qualifications

  • QualificationsMinimum 3 years of clinical research experience
  • Oncology experience is required
  • Prior involvement in NCI trials and federally funded research
  • Bachelor's degree in a science-related field
  • Key Responsibilities:Manage regulatory submissions, including IRB documentation

Benefits

  • Pay and BenefitsThe pay range for this position is $35.00 - $39.00/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 TypeThis is a fully onsite position in Merced,CA.Application DeadlineThis position is anticipated to close on Aug 22, 2025.About Actalent Actalent is a global leader in engineering and sciences services and talent solutions

Responsibilities

  • Serve as the primary point of contact for sponsors (excluding budget and contracting)Conduct informed consent discussions with patients
  • Coordinate scheduling for standard-of-care procedures
  • Ensure accountability and compliance for Investigational Products (IP)Collaborate with nursing staff for blood draw coordination
  • Maintain direct communication with Principal Investigators and actively manage PI engagement


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