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Job Title: Clinical Research Coordinator

Job Description

This role involves direct patient interaction, screening and recruitment, managing source documentation, and documenting in electronic medical records (EMR). You will be responsible for ordering labs and ensuring protocol compliance. While data entry is managed by a separate team, you will work closely with patients enrolled in oncology trials, guiding them through their therapy journey.

Responsibilities

+ Screen, consent, and enroll patients in oncology trials.

+ Monitor patients throughout their therapy, ensuring protocol compliance.

+ Collaborate with clinic staff to schedule appointments, including EKGs and vitals.

+ Interact with nursing staff, medical assistants, and clinical team for insurance authorizations.

+ Work alongside infusion nurses to schedule treatment appointments.

+ Maintain a patient-focused approach with enthusiasm and dedication.

+ Ensure research procedures outside clinical norms are completed accurately and timely.

Essential Skills

+ Minimum of 2 years of clinical research coordinator experience.

+ Proficiency in clinical research, pre-screening patients, oncology chart review, and patient recruitment.

+ Bachelor's degree in a relevant field.

Additional Skills & Qualifications

+ Experience with patient study enrollment is required.

+ Ability to read protocols, identify side effects, and assist patients in managing them.

+ Strong organizational skills.

+ Tuition reimbursement available.

+ ACRP membership fees and conference attendance may be sponsored.

Work Environment

The role allows the CRC to engage in cutting-edge oncology research. Trials include pharmaceutical-sponsored Phase I and II, investigator-led trials, and cooperative group trials. You will work within disease-specific teams in the cancer center, collaborating with data management staff. The position is full-time, Monday to Friday, 8 AM to 5 PM, with some flexibility based on clinic schedules. Office visits require daily on-site presence.

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 Jun 2, 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.

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 due to a disability, please email [email protected] (%[email protected]) for other accommodation options.