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Tmf Associate Jobs in Chicago, IL (NOW HIRING)

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Senior Clinical Research Associate

Chicago, IL · Hybrid

$110K - $138K/yr

Senior Clinical Research Associate - Oncology Phase I - Chicago ICON is a global healthcare ... Manage site essential document collection and TMF reconciliation with site files * Support sites ...

ICON

Senior Clinical Research Associate

Chicago, IL · On-site +1

$110K - $138K/yr

Senior Clinical Research Associate - Oncology Phase I - Chicago ICON is a global healthcare ... Manage site essential document collection and TMF reconciliation with site files * Support sites ...

IQVIA

CRA 1, IQVIA Biotech

Chicago, IL

$71K - $145K/yr

Job Overview The Clinical Research Associate I (CRA I) plays a key role in supporting the ... TMF) and the Investigator Site File (ISF). A central part of this role involves building and ...

IQVIA

CRA 1, IQVIA Biotech

Chicago, IL · On-site

$71K - $145K/yr

Job Overview The Clinical Research Associate I (CRA I) plays a key role in supporting the ... TMF) and the Investigator Site File (ISF). A central part of this role involves building and ...

IQVIA

CRA 1, IQVIA Biotech

Rosemont, IL

$71K - $145K/yr

Job Overview The Clinical Research Associate I (CRA I) plays a key role in supporting the ... TMF) and the Investigator Site File (ISF). A central part of this role involves building and ...

IQVIA

CRA 1, IQVIA Biotech

Rosemont, IL · On-site

$71K - $145K/yr

Job Overview The Clinical Research Associate I (CRA I) plays a key role in supporting the ... TMF) and the Investigator Site File (ISF). A central part of this role involves building and ...

All JobsTmf Associate JobsTmf Associate Jobs in Chicago, IL

Tmf Associate information

See Chicago, IL salary details

$17

$41

$72

How much do tmf associate jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for tmf associate in Chicago, IL is $41.19, according to ZipRecruiter salary data. Most workers in this role earn between $33.17 and $45.34 per hour, depending on experience, location, and employer.

What is the difference between Tmf Associate vs Tmf Analyst?

AspectTmf AssociateTmf Analyst
Required CredentialsBachelor's degree in life sciences, pharmacy, or related fields; basic knowledge of clinical trial processesBachelor's or master's degree; deeper understanding of TMF processes and regulatory requirements
Work EnvironmentClinical research organizations, pharmaceutical companies, or CROs; supporting TMF documentationMore analytical role within similar settings; involved in reviewing and ensuring compliance
Employer & Industry UsageCommonly used in clinical trial documentation teamsUsed in quality assurance and compliance teams within the same industry

The main difference between a Tmf Associate and a Tmf Analyst lies in their experience level and scope of responsibilities. Tmf Associates typically handle documentation support and basic compliance tasks, while Tmf Analysts perform more detailed reviews and analysis to ensure regulatory adherence. Both roles are essential in clinical trial management, with the Analyst position requiring a deeper understanding of TMF processes.

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For Tmf Associate jobs in Chicago, IL, the most frequently searched job titles are:

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The top searched job categories for Tmf Associate jobs in Chicago, IL are:

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Cities near Chicago, IL with the most Tmf Associate job openings:

Tmf Associate jobs near you
Infographic showing various Tmf Associate job openings in Chicago, IL as of July 2026, with employment types broken down into 1% As Needed, 70% Full Time, 27% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $85,749 per year, or $41.2 per hour.

Senior Clinical Research Associate

Barrington James

Chicago, IL • On-site

Other

Posted 21 days ago

Job description

New Role - Snr CRA - Small CRO - US Only


Key Responsibilities


  • Independently perform site selection, initiation, routine monitoring, and close-out visits in accordance with the protocol, ICH-GCP, and applicable regulations
  • Conduct/oversee remote and on-site monitoring visits, ensuring source data verification, informed consent compliance, and data quality
  • Manage a defined caseload of sites with minimal supervision, ensuring enrollment, timelines, and quality metrics are met
  • Serve as primary site contact, building strong relationships with investigators and site staff
  • Identify and resolve site-level issues, escalating risks to the Clinical Team Lead/PM as appropriate
  • Review and ensure completeness of essential documents/TMF in line with ICH-GCP and company SOPs
  • Support development of monitoring plans, visit report templates, and site management tools
  • Mentor and provide guidance to junior CRAs and CRA-in-training staff
  • Contribute to audit/inspection readiness at site and study level
  • Liaise directly with sponsors on site status, risk mitigation, and study progress as needed
  • Support process improvement initiatives given the CRO's smaller, evolving infrastructure


Requirements


  • Bachelor's degree in life sciences, nursing, or related field (or equivalent experience)
  • Minimum 3–5 years' CRA experience, including independent on-site monitoring (CRO, sponsor, or site-based)
  • Strong working knowledge of ICH-GCP, FDA/EMA (or relevant regional) regulations
  • Proven track record managing a full monitoring visit caseload independently
  • Experience in [therapeutic area, if relevant] preferred
  • Excellent communication and site relationship management skills
  • Ability to work autonomously in a smaller, less hierarchical company structure
  • Willingness to travel 30% for on-site visits (region-dependent)
  • Experience mentoring junior staff is a plus


Tbacchus@barringtonjames.com

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