Clinical Research Coordinator

Actalent; Chicago (IL); On-site; USD 40,000 - 44,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) retirement plan

Life Insurance

Job summary

Actalent in Chicago, IL is seeking a Clinical Research Coordinator to manage participant visits, regulatory documentation, and study operations across multiple trials. You will support investigators, sponsors, and monitors while upholding data quality and safety standards.

The role requires a minimum of 2 years’ CRO experience, regulatory expertise, and strong communication with participants and teams. This onsite position offers a fast-paced environment and career growth within clinical

Qualifications

• At least 2 years of experience as a Clinical Research Coordinator on industry-sponsored clinical trials.
• Hands-on experience with clinical research operations, including patient screening, visit coordination, and trial logistics.
• Proven experience preparing and maintaining regulatory documentation per FDA, ICH, and GCP standards.
• Experience with regulatory file management and source documentation.
• Experience with cardiometabolic, metabolic, endocrine, or internal medicine trials.

Responsibilities

• Coordinate participant visits, scheduling, assessments, and follow-ups with accuracy and professionalism.
• Drive day-to-day study operations across multiple trials while meeting protocol requirements.
• Perform venipuncture and process specimens safely per protocols and guidelines.
• Maintain complete regulatory files and source documentation in line with GCP and sponsor requirements.
• Lead recruitment and screening to ensure eligible and timely enrollment.

Skills

Clinical Research Coordinator

Clinical operations

Regulatory documentation

Cardiometabolic trials

Regulatory file management

Organizational skills

Communication

Teamwork

Education

Bachelor's degree

CCRC credential

Job description

Job Title: Clinical Research Coordinator

Job Description

The Clinical Research Coordinator plays a central role in the successful execution of industry-sponsored clinical trials. In this position, you serve as the trusted point of contact for participants, the operational backbone of each study, and a key partner to investigators, sponsors, contract research organizations, and monitors. You coordinate participant visits and procedures, maintain meticulous regulatory and source documentation, and support cardiometabolic and other therapeutic area trials with a strong commitment to participant safety and data quality.

Responsibilities

• Coordinate all aspects of the participant experience, including scheduling and managing study visits, assessments, and follow-up appointments with accuracy, care, and professionalism.
• Drive day-to-day study operations across multiple active clinical trials simultaneously, ensuring that protocol requirements and timelines are consistently met.
• Perform venipuncture and process laboratory specimens safely and accurately in accordance with study protocols and applicable guidelines.
• Maintain complete and compliant source documentation and regulatory files, adhering to Good Clinical Practice (GCP), FDA, ICH, and sponsor requirements.
• Lead participant recruitment and screening activities, ensuring appropriate eligibility assessment and timely enrollment into clinical trials.
• Support participant retention by building rapport, providing clear education about study procedures, and coordinating ongoing study engagement.
• Identify, document, and report adverse events and other safety information promptly, helping to safeguard participant well-being and overall study integrity.
• Collaborate closely with investigators, sponsors, monitors, and other research staff to prepare for and support monitoring visits, audits, and other oversight activities.
• Ensure regulatory documentation is accurate, up to date, and organized, including informed consent forms and other essential regulatory records.
• Contribute to the smooth operation of cardiometabolic, metabolic, endocrine, and internal medicine-related trials through effective coordination and communication.

Essential Skills

• At least 2 years of experience as a Clinical Research Coordinator on industry-sponsored clinical trials.
• Hands-on experience with clinical research operations, including patient screening, visit coordination, and trial logistics.
• Proven experience preparing and maintaining regulatory documentation in accordance with FDA, ICH, and GCP standards.
• Knowledge of clinical trial processes and requirements, including source documentation and regulatory file management.
• Experience working on cardiometabolic, metabolic, endocrine, or internal medicine-related clinical trials.
• Ability to identify, document, and report adverse events and other safety-related information accurately and promptly.
• Strong organizational skills with the ability to manage multiple concurrent clinical trials and competing priorities.
• Effective communication and interpersonal skills to serve as a reliable point of contact for participants and study stakeholders.
• Attention to detail and commitment to high-quality data collection and documentation.
• Ability to work collaboratively within a multidisciplinary clinical research team.

Additional Skills & Qualifications

• Phlebotomy experience, including venipuncture and specimen processing, is strongly preferred.
• Bachelor’s degree is strongly preferred; a Certified Clinical Research Coordinator (CCRC) credential is considered a plus.
• High school diploma or associate degree may be considered with relevant clinical research experience.
• Experience with patient recruitment strategies in clinical trials, particularly in areas such as diabetes and endocrinology.
• Familiarity with clinical research in psychiatric, sleep, psychedelics, vaccine, and general medicine indications is beneficial.
• Comfort working with regulatory frameworks and guidelines related to clinical trials.
• Demonstrated ability to educate participants about study procedures and expectations in a clear and supportive manner.

Work Environment

This role is based primarily at a dedicated clinical research site in the Portage Park area, serving the greater Chicagoland community. The facility has a long-standing history of conducting a high volume of clinical trials across diverse therapeutic areas, supported by board-certified physicians, licensed clinicians, psychometricians, and experienced research professionals. You work in a structured, well-managed environment focused on participant safety, data quality, and operational excellence. The setting includes typical clinical research equipment and spaces for participant visits, assessments, and specimen collection. You collaborate closely with a multidisciplinary team and interact regularly with monitors and sponsors. The work involves on-site coordination of study visits and procedures during standard clinical research operating hours, with professional attire appropriate for a patient-facing, clinical setting.

Job Type & Location

This is a Contract to Hire position based out of Chicago, IL.

Pay And Benefits

The pay range for this position is $29.00 - $31.50/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 Chicago,IL. Application Deadline This position is anticipated to close on Aug 24, 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.