Job Title: Clinical Research Coordinator Job Description We are seeking a Clinical Research Coordinator with a minimum of 3 years of clinical research experience, with 7+ years preferred for sr-level consideration. The candidate must have oncology experience and demonstrate proven ability to communicate directly with Principal Investigators (PIs) and sponsors. This role requires initiative and independence, as it is a solo position at the site, sharing space with a nurse lead. Responsibilities + Perform regulatory tasks, such as IRB submissions. + Maintain sponsor correspondence, excluding budget and contracting. + Facilitate the informed consent process. + Schedule standard-of-care procedures. + Ensure investigational product (IP) accountability. + Collaborate with local nurses for blood draws. + Maintain direct communication with investigators and actively manage client engagement. Essential Skills + Pre-screening patients + Clinical research + Oncology expertise + Clinical trial management + Knowledge of Good Clinical Practice (GCP) + IRB regulatory knowledge + Recruitment skills + Data entry proficiency + Electronic Data Capture (EDC) systems + Experience with National Cancer Institute (NCI) trials Additional Skills & Qualifications + Prior involvement in NCI trials and federally funded research Work Environment The work environment is mission-driven with a patient-first approach and a growing research portfolio. You will be the solo coordinator onsite, requiring the ability to work independently with clients. The position offers robust onboarding and streamlined training, tuition reimbursement for further education, and weekly mentorship support. Pay and Benefits The 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 Type This is a fully onsite position in Merced,CA. Application Deadline This position is anticipated to close on Aug 20, 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.