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Tmf Associate Jobs in Illinois (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

Bloomington, 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

Bloomington, 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 ...

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All JobsTmf Associate JobsTmf Associate Jobs in Illinois

Tmf Associate information

See Illinois salary details

$16

$38

$68

How much do tmf associate jobs pay per hour?

As of Sep 1, 2026, the average hourly pay for tmf associate in Illinois is $38.75, according to ZipRecruiter salary data. Most workers in this role earn between $31.20 and $42.64 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.

What are the most commonly searched types of Tmf jobs in Illinois?

The most popular types of Tmf jobs in Illinois are:

What are popular job titles related to Tmf Associate jobs in Illinois?

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

What job categories do people searching Tmf Associate jobs in Illinois look for?

The top searched job categories for Tmf Associate jobs in Illinois are:

What cities in Illinois are hiring for Tmf Associate jobs?

Cities in Illinois with the most Tmf Associate job openings:

Tmf Associate jobs near you
Infographic showing various Tmf Associate job openings in Illinois as of June 2026, with employment types broken down into 100% Full Time. Highlights an 46% In-person, 27% Hybrid, and 27% Remote job distribution, with an average salary of $80,593 per year, or $38.7 per hour.

Senior Clinical Research Associate

Chicago, IL • On-site

Barrington James
See more jobs at Barrington Jamesexternal

Other

This job post has expired today. Applications are no longer accepted.

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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