Actalent
Oncology Clinical Research Coordinator
MUST already reside in Merced, CA area as interviews will be in person. Qualifications: Minimum 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 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 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 22, 2025.
MUST already reside in Merced, CA area as interviews will be in person. Qualifications: Minimum 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 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 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 22, 2025.