Clinical Research Associate

Job Title: Clinical Research Associate (Must have oncology experience) Job Description This Clinical Research Associate role focuses on data management and clinic coordination for oncology clinical trials, with a balanced mix of patient-facing responsibilities and data-focused tasks. The position supports the full lifecycle of clinical studies by conducting pre-screening, recruitment, consenting, specimen coordination, and follow-up activities, while collaborating closely with physicians and research staff. The role requires frequent use of electronic data capture systems and clinical platforms such as EPIC, and offers opportunities for professional growth through ongoing training. Responsibilities

- Coordinate day-to-day activities for oncology clinical trials, focusing on both data management and clinic operations.
- Conduct chart reviews and pre-screen patients to identify eligible participants for oncology clinical trials.
- Recruit and consent patients for clinical studies, joining the physician during visits to support the informed consent process.
- Coordinate specimen collection for clinical trials, ensuring proper handling, documentation, and tracking in alignment with study protocols.
- Perform follow-up activities with study participants, maintaining accurate and timely documentation of all patient interactions.
- Enter and manage study data in electronic data capture (EDC) systems and other clinical databases, ensuring accuracy, completeness, and compliance with study requirements.
- Work extensively within EPIC and other clinical or research systems to document patient information and trial-related data.
- Participate in regular meetings, dedicating approximately 1020% of working time to study-related discussions, updates, and team coordination.
- Split remaining time evenly between data-focused tasks and direct patient interaction to support both operational and clinical aspects of the trials.
- Collaborate closely with a research nurse and another research assistant to ensure smooth execution of all study-related activities.
- Engage in ongoing training and development to expand knowledge of clinical research processes, systems, and oncology trials.

Essential Skills

- At least 1 year of clinical research experience, including hands-on involvement with clinical trials in oncology.
- Experience with clinical trial workflows, including pre-screening, recruitment, consenting, and follow-up of study participants.
- Proficiency in chart review to identify and assess potential candidates for oncology clinical trials.
- Demonstrated experience in data entry and data management within clinical research settings.
- Familiarity with electronic data capture (EDC) systems, with the ability to learn and adapt to a variety of platforms.
- Experience working within clinical systems such as EPIC or similar electronic medical record platforms.
- Understanding of clinical research practices, including coordination of specimen collection and documentation of patient interactions.
- Ability to balance patient-facing responsibilities with detailed data management tasks.
- Strong organizational skills with attention to detail and accuracy in documentation.

Additional Skills & Qualifications

- Previous experience supporting oncology research in a clinical setting.
- Demonstrated ability to learn new software systems and adapt to multiple EDC platforms.
- Experience collaborating with multidisciplinary clinical teams, including physicians, research nurses, and research assistants.
- Interest in professional development and willingness to participate in ongoing training and growth opportunities related to clinical research.

Work Environment The role is primarily based at a cancer center in Novi, where the Clinical Research Associate will spend the majority of their time. There may be occasional travel to additional cancer center locations, such as Southfield or a downtown site, with mileage reimbursement provided for these trips. The associate will work closely with a research nurse and another research assistant, and will also connect regularly with colleagues at another location through daily huddles. The work environment is clinical and research-focused, with frequent use of EPIC and various electronic data capture systems to support oncology trials. The position involves a mix of office-based data work and direct interaction with patients in a clinical setting.
Job Type & Location
This is a Contract position based out of Novi, MI.
Pay and Benefits
The pay range for this position is $20.00 - $26.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors. 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 Novi,MI.
Application Deadline
This position is anticipated to close on Oct 16, 2026. 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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

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 [email protected] for other accommodation options.

San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.

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It is unlawful in Massachusetts to require or administer a lie detector test as a
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shall be subject to criminal penalties and civil liability.

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