Job Title: Clinical Research Coordinator
Job Description

We are seeking a dedicated and enthusiastic Clinical Research Coordinator to join our team. This role is focused on patient-facing activities, including screening, recruitment, managing source documentation, and documenting in EMR. The coordinator will not be responsible for data entry or specimen collection, but will manage patient interactions and protocol compliance for oncology trials.

ResponsibilitiesScreen, consent, and enroll patients in oncology trials, following patients through the course of their therapy.Spend most of the time in clinic, seeing patients with doctors, attending patient visits, ensuring completion of questionnaires, and conducting research procedures.Work with clinic staff to schedule appointments, such as EKGs and vitals.Ensure protocol compliance by adhering to correct timeframes.Interact and collaborate with nursing staff, medical assistants, and clinical staff for insurance authorizations and scheduling.Work closely with infusion nurses to schedule patient appointments.Support patients by providing them with specific calendars and checklists for their participation in the study, and help them manage side effects.Essential SkillsClinical research experience (1-2 years for ACRC, 2-4 years for CRC, 4+ years for Senior CRC in oncology).Proficiency in pre-screening patients, chart review, and patient recruitment.Experience in oncology clinical studies, including screening, consenting, and source documentation.Strong organizational skills and the ability to read protocols and notice side effects.Bachelor's degree.Additional Skills & QualificationsExperience with patient study enrollment and assisting patients with study requirements.Ability to provide support for oncology patients, considering their serious health conditions.Work Environment

The Clinical Research Coordinator will work in a comprehensive cancer center that is at the forefront of oncology research, participating in novel treatments and working with dedicated investigators. The role involves managing various types of trials, including pharmaceutical-sponsored trials, investigator-initiated trials, and national clinical trials. The clinical group is divided into disease teams, and candidates will be assigned based on their experience and business needs. The work schedule is Monday to Friday, 8 AM to 5 PM, with some flexibility based on the clinic schedule. The coordinator must be on-site for office visits daily.

Pay and Benefits

The pay range for this position is $30.00 - $40.00

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 will be accepting applications until Jan 4, 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 actalentaccommodation@actalentservices.com for other accommodation options.