Clinical Research Coordinator

Job Title: Clinical Research Coordinator
Job Description
We are seeking a dedicated Clinical Research Coordinator to join our dynamic team. This role involves patient-facing duties, including screening, recruitment, and managing source documentation. You will document in EMR, order labs, and manage patient appointments. You will be responsible for screening, consenting, and enrolling patients on oncology trials and following them through the course of their therapy.
Responsibilities

• Screen, consent, and enroll patients in oncology trials.
• Manage patient visits and ensure questionnaires and research procedures are completed.
• Work with clinic staff to schedule appointments, such as EKGs or vitals.
• Ensure protocol compliance and timely completion of tasks.
• Interact with nursing staff and medical assistants.
• Collaborate with clinical staff for insurance authorizations and scheduling.
• Work closely with infusion nurses to arrange appointments.
• Assist patients with understanding their calendar of events and participation requirements.

Essential Skills

• Experience in patient study enrollment and managing study requirements.
• Ability to read protocols, notice side effects, and assist patients.
• Bachelor's degree in a relevant field.
• Proficiency in clinical research, patient pre-screening, oncology, and chart review.
• Strong organizational skills and attention to detail.

Additional Skills & Qualifications

• ACRC Exam/Certification reimbursement.
• ACRP membership fees covered and potential conference attendance.
• Tuition reimbursement programs available.
• Experience in dealing with oncology patients and understanding their needs.

Work Environment
The work involves various types of trials, including pharmaceutical-sponsored Phase I and II, some Phase III, investigator-led protocols, and trials funded by national clinical trial groups. The clinical group is divided into disease teams and works closely with data management staff. The position requires being on-site daily for office visits, with a typical schedule of Monday to Friday, 8 AM to 5 PM, with some flexibility based on the clinic schedule. Working in the Comprehensive Cancer Center offers a prestigious opportunity to be at the cutting edge of oncology research.
Pay and Benefits
The pay range for this position is $30.00 - $40.00/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 Sacramento,CA.
Application Deadline
This position is anticipated to close on Feb 14, 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.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

• Hiring diverse talent
• Maintaining an inclusive environment through persistent self-reflection
• Building a culture of care, engagement, and recognition with clear outcomes
• Ensuring growth opportunities for our people

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 process due to a disability, please email for other accommodation options.