Part-Time Clinical Research Coordinator

Actalent; Glenview (IL); On-site; USD 41,000 - 55,000; Part time

Benefits offered by this job

Medical benefits

401(k) plan

Paid time off

Job summary

Actalent is seeking a part-time Clinical Research Coordinator in Glenview, IL to support clinical trials within a clinic setting. You will coordinate trial activities, assist with patient recruitment and informed consent, and ensure regulatory compliance and accurate documentation.

You will maintain study data in EDC/EMR systems, support regulatory submissions, and liaise with investigators and staff. 16–24 hours/week with on-site presence in a professional clinic environment.

Qualifications

• Minimum 12 months experience as CRC or in a related clinical research role.
• Strong understanding of clinical trial processes including start-up, recruitment, consent, screening, enrollment and follow-up.
• Solid knowledge of GCP guidelines and applicable regulatory requirements.
• Demonstrated experience with chart review and patient recruitment in clinical/research settings.
• Proficiency with EDC systems and EMR platforms.
• Ability to maintain regulatory and study documentation in compliance with protocols.
• Excellent organizational skills to manage multiple tasks and timelines.
• Strong problem-solving and attention to detail for high-quality data.
• Effective verbal and written communication with participants, investigators, and cross-functional teams.
• Strong interpersonal skills to build rapport with patients and staff.
• Proficiency in Microsoft Office (Word, Excel, Outlook).
• Ability to learn CTMS and related research platforms.

Responsibilities

• Coordinate and implement clinical trial activities per study protocols including recruitment and enrollment.
• Conduct chart reviews to pre-screen potential participants based on eligibility criteria.
• Support recruitment by communicating with prospective participants and guiding informed consent.
• Maintain accurate regulatory files in compliance with GCP and regulations.
• Oversee data collection and entry into study databases/EDC systems with quality control.
• Use EMR systems to obtain and verify clinical information for procedures.
• Assist with regulatory documents and IRB communications, including amendments and safety reports.
• Serve as a liaison among study site, participants, investigators, and internal teams.
• Manage logistics for study visits and ensure availability of materials and supplies.
• Support procedures such as phlebotomy within scope of training when applicable.
• Monitor study activities for adherence to protocol and report deviations timely.
• Provide mentorship to junior staff and share best practices in clinical research.

Skills

CRC experience

Clinical trial processes

GCP compliance

Chart review

EDC proficiency

EMR platforms

Regulatory documentation

CTMS familiarity

Microsoft Office

Communication skills

Organizational skills

Problem-solving

Team collaboration

Phlebotomy (within scope)

Tools

CTMS

EMR

EDC systems

Job description

Job Title: Clinical Research CoordinatorJob Description

This part-time Clinical Research Coordinator role supports the successful execution of clinical trials within a clinic environment. The position focuses on coordinating day-to-day study activities, supporting patient recruitment and enrollment, maintaining accurate documentation, and ensuring compliance with protocols, Good Clinical Practice (GCP), and applicable regulatory requirements. The role offers the opportunity to contribute to meaningful clinical research while working with one of the leading healthcare providers in the United States.

Responsibilities

• Coordinate and implement clinical trial activities in accordance with study protocols, including patient recruitment, informed consent, screening, and enrollment support as delegated by the Principal Investigator.
• Conduct thorough chart reviews to identify and pre-screen potential study participants based on protocol-specific eligibility criteria.
• Support patient recruitment efforts by communicating with prospective participants, explaining study procedures, and facilitating the informed consent process.
• Maintain accurate, complete, and up-to-date study documentation and regulatory files in compliance with GCP, institutional policies, and applicable regulations.
• Oversee or support data collection and data entry into study databases and electronic data capture (EDC) systems, ensuring data quality, accuracy, and adherence to protocol requirements.
• Utilize electronic medical record (EMR) systems to obtain and verify clinical information required for study procedures and documentation.
• Assist with the preparation, submission, and tracking of regulatory documents and correspondence to regulatory authorities and Institutional Review Boards (IRBs), including protocol amendments and safety reports.
• Act as a liaison between the study site, participants, investigators, and internal teams to facilitate effective communication and problem resolution.
• Manage logistics for study visits, including scheduling participants, coordinating with clinic staff, and ensuring the availability of study materials, supplies, and equipment.
• Support study-related procedures, which may include tasks such as phlebotomy when within scope of practice and training.
• Monitor ongoing study activities to ensure adherence to protocol, GCP, and regulatory requirements, and promptly report any issues or deviations to the appropriate parties.
• Provide mentorship and guidance to junior staff when applicable, sharing best practices and supporting their development in clinical research processes.

Essential Skills

• Minimum of 12 months of experience as a Clinical Research Coordinator (CRC) or in a closely related clinical research role.
• Strong understanding of clinical trial processes, including study start-up, patient recruitment, informed consent, screening, enrollment, and follow-up.
• Solid knowledge of Good Clinical Practice (GCP) guidelines and applicable regulatory requirements for clinical research.
• Demonstrated experience with chart review and patient recruitment in a clinical or research setting.
• Proficiency with electronic data capture (EDC) systems and electronic medical record (EMR) platforms.
• Ability to maintain accurate and complete regulatory and study documentation in compliance with protocols and regulations.
• Excellent organizational skills with the ability to manage multiple tasks, priorities, and timelines in a fast-paced environment.
• Strong problem-solving skills and attention to detail to ensure high‑quality data and protocol compliance.
• Effective verbal and written communication skills for interacting with participants, investigators, and cross‑functional teams.
• Strong interpersonal skills to build rapport with patients and collaborate effectively with clinical and research staff.
• Proficiency in Microsoft Office applications, including Word, Excel, and Outlook.
• Ability to learn and work within clinical trial management systems (CTMS) and related research platforms.

Additional Skills & Qualifications

• Cardiology clinical research experience is preferred but not required.
• Experience performing or supporting phlebotomy procedures within scope of training is an advantage.
• Prior experience working in a clinic‑based research environment is beneficial.
• Familiarity with CTMS and other clinical research technology platforms is highly desirable.
• Demonstrated ability to act as a liaison between multiple stakeholders, including patients, investigators, and internal teams.
• Experience mentoring or guiding junior staff is a plus.
• Genuine interest in contributing to clinical research trials and improving patient care through evidence-based medicine.

Work Environment

This is an on‑site, part‑time position based in a clinic environment, typically ranging from 16 to 24 hours per week. You will work closely with clinical and research professionals in a setting focused on delivering high‑quality patient care while conducting clinical research trials. The role involves regular use of electronic medical record (EMR) systems, electronic data capture (EDC) platforms, clinical trial management systems (CTMS), and standard office software such as Microsoft Office. The clinic environment is structured and professional, with direct interaction with patients and multidisciplinary teams. The schedule provides some flexibility within the part‑time hours while maintaining consistent on‑site presence to support study visits and trial activities. This position offers the opportunity to contribute to impactful clinical research within a leading healthcare organization.

Job Type & Location

This is a Contract position based out of Glenview, IL.

Pay and Benefits

The pay range for this position is $30.00 - $40.00/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 Glenview,IL.

Application Deadline

This position is anticipated to close on Oct 23, 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 [e-mail] 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.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.