Clinical Research Coordinator

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.

Combine two of the fastest-growing fields on the planet with a culture of performance, collaboration and opportunity and this is what you get. Leading edge technology in an industry that is improving the lives of millions. Here, innovation is not about another gadget; it is about making health care data available wherever and whenever people need it, safely and reliably. There is no room for error. If you are looking for a better place to use your passion and your desire to drive change, this is the place to be. It's an opportunity to do your life's best work. (sm)

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.

Primary Responsibilities:

Study Coordination & Participant Management

• Screens, recruits, and enrolls eligible oncology patients into clinical trials
• Conducts informed consent discussions and documents per regulatory guideline
• Schedules and coordinates participant study visits, assessments, and procedure
• Monitors participant safety, reports adverse events, and ensures appropriate follow‑up

Protocol Compliance & Study Execution

• 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

What are the reasons to consider working for UnitedHealth Group?  Put it all together - competitive base pay, a full and comprehensive benefit program, performance rewards, and a management team who demonstrates their commitment to your success. Some of our offerings include:

• 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.)

You'll be rewarded and recognized for your performance in an environment that will challenge you and give you clear directions on what it takes to succeed in your role as well as provide development for other roles you may be interested in.

Required Qualifications:

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

Preferred Qualifications:

• 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

Pay is based on several factors including but not limited to local labor markets, education, work experience, certifications, etc. In addition to your salary, we offer benefits such as, a comprehensive benefits package, incentive and recognition programs, equity stock purchase and 401k contribution (all benefits are subject to eligibility requirements). No matter where or when you begin a career with us, you'll find a far-reaching choice of benefits and incentives. The hourly pay for this role will range from $17.98 to $32.12 per hour based on full-time employment. We comply with all minimum wage laws as applicable.

At UnitedHealth Group, our mission is to help people live healthier lives and make the health system work better for everyone. We believe everyone-of every race, gender, sexuality, age, location, and income-deserves the opportunity to live their healthiest life. Today, however, there are still far too many barriers to good health which are disproportionately experienced by people of color, historically marginalized groups, and those with lower incomes. We are committed to mitigating our impact on the environment and enabling and delivering equitable care that addresses health disparities and improves health outcomes - an enterprise priority reflected in our mission.

UnitedHealth Group is an Equal Employment Opportunity employer under applicable law and qualified applicants will receive consideration for employment without regard to race, national origin, religion, age, color, sex, sexual orientation, gender identity, disability, or protected veteran status, or any other characteristic protected by local, state, or federal laws, rules, or regulations.

UnitedHealth Group is a drug - free workplace. Candidates are required to pass a drug test before beginning employment.

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