Clinical Research Coordinator

UnitedHealth Group • Las Vegas, NV

10d • $20 - $36 • Onsite

About The Position

Optum is a global organization that delivers care, aided by technology to help millions of people live healthier lives. The work you do with our team will directly improve health outcomes by connecting people with the care, pharmacy benefits, data and resources they need to feel their best. Here, you will find a culture guided by inclusion, talented peers, comprehensive benefits and career development opportunities. Come make an impact on the communities we serve as you help us advance health optimization on a global scale. Join us to start Caring. Connecting. Growing together.
Optum Care Cancer Care of Nevada is committed to offering patients compassion, innovation, and high-quality care.
Schedule: – A 40-hour work week. Monday through Friday between the hours of 7:30am to 4:00 pm
Location: 2300 Charleston Boulevard Las Vegas, NV
Positions in this function are responsible for managing clinical studies and assisting other functions as appropriate in execution of their tasks. Updates process as necessary to ensure efficiency and accuracy.

Requirements

• High School Diploma/GED
• 2+ years of clinical research experience, preferably in oncology
• 1+ years of experience in ICH‑GCP, FDA regulations, and Good Documentation Practices
• 1+ years of experience in strong organizational skills, attention to detail, and ability to manage multiple studies
• 1+ years of experience in excellent communication skills and comfort working directly with patients
• Intermediate level of proficiency with Microsoft Office Application

Nice To Haves

• Bachelor’s degree in health sciences or related field (or equivalent experience)
• Certification: ACRP-CP, CCRC, or SOCRA CCRP
• Experience with oncology trials (pharma-sponsored, device, or cooperative group)
• Experience with EMR (EPIC), eRegulatory systems (CRIO), and CTMS platforms (CRIO)
• Phlebotomy or specimen handling experience

Responsibilities

• Screens, recruits, and enrolls eligible oncology patients into clinical trials
• Conducts informed consent discussions and documents per regulatory guidelines
• Schedules and coordinates participant study visits, assessments, and procedures
• Monitors participant safety, reports adverse events, and ensures appropriate follow‑up
• Reviews study protocols and prepare study workflows with the research team
• Coordinates specimen collection, processing, storage, and shipment to central labs
• Works closely with physicians and clinical staff to ensure protocol adherence

Benefits

• Paid Time Off which you start to accrue with your first pay period plus 8 Paid Holidays
• Medical Plan options along with participation in a Health Spending Account or a Health Saving account
• Dental, Vision, Life& AD&D Insurance along with Short-term disability and Long-Term Disability coverage
• 401(k) Savings Plan, Employee Stock Purchase Plan
• Education Reimbursement
• Employee Discounts
• Employee Assistance Program
• Employee Referral Bonus Program
• Voluntary Benefits (pet insurance, legal insurance, LTC Insurance, etc.)

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: High school or GED