Job Title: Clinical Research Coordinator
Job Description

We are seeking a Clinical Research Coordinator to join our team in the downtown location. This role is a backfill for our consultant, who will not be transitioning to a permanent position. The successful candidate will work closely with multidisciplinary teams, including sponsors, project stakeholders, and the data team, to manage the daily operations of biomedical and social-behavioral research studies. The specific subspecialty will depend on the coordinator's previous experience.

ResponsibilitiesManage the daily operations of research studies involving multidisciplinary teams.Monitor study performance, analyze and review results, and supervise the development and implementation of new protocols.Ensure completion of study activities per protocol.Collaborate with nursing staff and the Principal Investigator to ascertain pretreatment and eligibility requirements, conduct participant interviews, and obtain social and medical histories.Organize patient treatment and test schedules, including enrolling and consenting patients.Conduct experimental tests and procedures and closely monitor and document adverse events.Manage project data, ensuring accuracy, analysis, and evaluation to meet project objectives.Partner with internal and external project and IT staff to create, review, analyze, interpret, and summarize progress and final reports.Provide consultation on data management, methodological issues, and data analysis.Ensure effective data flow for oncology research clinical trials and chemoprevention studies.Collaborate with internal and external staff, including sponsoring agencies and research institutions, to meet project objectives and timelines.Advise on enhancements to processes, practices, and procedures to ensure compliance with protocols.Manage day-to-day project operations and ensure compliance with local, state, and federal regulatory guidelines.Essential SkillsBachelors degree1-2 years of experience working on drug or device studiesExperience with protocols, patient recruitment, and EMR systemsKnowledge of clinical data, monitoring tools, and GCP guidelinesExperience with oncology, cardiology, or neurology studiesAdditional Skills & QualificationsExperience with patient recruitment, chart review, and data entryPhlebotomy skills and experience in specimen processingFamiliarity with Medidata, EPIC, and Advarra systemsExperience with multi-site studies and industry-based studiesExperience with regulatory submissions to local or central IRBsWork Environment

The team structure includes the Director of Oncology, Clinical Research Managers, Project Managers, CRC Leads, CRCs, and Data Coordinators. The work environment fosters collaboration and offers opportunities for career advancement. This role provides access to top-notch research facilities and a comprehensive benefits package, including competitive healthcare plans, retirement benefits, and significant tuition discounts. The organization is proud to support employees in maintaining healthy lifestyles and navigating life’s challenges and opportunities.

Pay and Benefits

The pay range for this position is $33.00 - $35.00/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 Chicago,IL.

Application Deadline

This position is anticipated to close on Feb 28, 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.