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Clinical Research Project Assistant Jobs in Normal, IL

Medi-Weightloss

Nurse Practitioner

Bloomington, IL

Medi-Weightloss is thrilled to invite an exceptional Nurse Practitioner or Physician Assistant to ... Our individualized treatment is supported by clinical research and translational science. License ...

IQVIA

CRA 1, IQVIA Biotech

Bloomington, IL · On-site

$71K - $145K/yr

Basic knowledge of clinical research regulations (GCP/ICH). * Ability to travel as required by the project. IQVIA is a leading global provider of clinical research services, commercial insights and ...

IQVIA

CRA 1, IQVIA Biotech

Bloomington, IL · On-site

$71K - $145K/yr

Basic knowledge of clinical research regulations (GCP/ICH). * Ability to travel as required by the project. IQVIA is a leading global provider of clinical research services, commercial insights and ...

Project Oz

Mental Health Specialist

Bloomington, IL · On-site

$44K/yr

Project Oz is looking for a full-time Mental Health Specialist to provide suicide prevention ... * Assist in the research and design of new program materials and delivery systems. * Refer ...

Project Oz

Mental Health Specialist

Bloomington, IL · On-site

Project Oz is looking for a full-time Mental HealthSpecialist to provide suicide prevention ... * Assist in the research and design of new program materials and delivery systems. * Refer ...

Memorial Health

RN - New Graduate

Lincoln, IL · On-site

$30.23 - $48.37/hr

... project. As a group you will work with your unit and unit manager on a clinical issue that you see ... They will provide age-appropriate care and will participate in research when appropriate and ...

Memorial Health

RN - New Graduate

Lincoln, IL

$30.23 - $48.37/hr

... project. As a group you will work with your unit and unit manager on a clinical issue that you see ... They will provide age-appropriate care and will participate in research when appropriate and ...

Memorial Health

RN - New Graduate

Lincoln, IL · On-site

$30.23 - $48.37/hr

... project. As a group you will work with your unit and unit manager on a clinical issue that you see ... They will provide age-appropriate care and will participate in research when appropriate and ...

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All JobsClinical Research Project JobsClinical Research Project Assistant JobsClinical Research Project Assistant Jobs in Normal, IL

Clinical Research Project Assistant information

See Normal, IL salary details

$7

$22

$45

How much do clinical research project assistant jobs pay per hour?

As of Jul 16, 2026, the average hourly pay for clinical research project assistant in Normal, IL is $22.20, according to ZipRecruiter salary data. Most workers in this role earn between $16.92 and $25.38 per hour, depending on experience, location, and employer.

What do clinical research assistants do?

Clinical research assistants support the conduct of clinical trials by preparing study materials, recruiting and screening participants, collecting and managing data, and ensuring compliance with protocols and regulations. They often work under the supervision of investigators and may use electronic data capture tools or databases as part of their responsibilities.

What is the difference between Clinical Research Project Assistant vs Clinical Research Coordinator?

AspectClinical Research Project AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are a plusRequires a bachelor's degree; certifications such as CCRP or CCR are common
Work EnvironmentSupports research teams in clinical settings, hospitals, or research institutionsManages daily clinical trial activities, interacts directly with patients and investigators
Employer & Industry UsageUsed by research institutions, hospitals, pharmaceutical companiesCommonly employed in clinical trial sites, hospitals, and research organizations

The Clinical Research Project Assistant primarily supports research activities and data management, while the Clinical Research Coordinator oversees trial operations and patient interactions. Both roles require similar educational backgrounds and certifications, but their responsibilities differ in scope and daily tasks.

How much money do clinical research assistants make?

Clinical research assistants typically earn a median annual salary of around $45,000 to $55,000, depending on experience, location, and the complexity of the research environment. Entry-level positions may start lower, while those with specialized skills or certifications can earn higher wages.

What does a research project assistant do?

A research project assistant supports the planning, coordination, and execution of clinical research studies. They handle tasks such as data collection, maintaining study documentation, scheduling participant visits, and ensuring compliance with protocols and regulations. Strong organizational skills and familiarity with research tools like electronic data capture systems are often required.

Is CRA an entry level job?

A Clinical Research Associate (CRA) is typically not an entry-level position; it usually requires prior experience in clinical research, such as a background in healthcare or life sciences, and often involves monitoring clinical trials. Entry-level roles in clinical research may include Clinical Trial Assistant or Research Coordinator, with CRAs generally needing several years of related experience or specialized training. Certifications like SOCRA or ACRP can also be beneficial for advancing to CRA roles.
What cities near Normal, IL are hiring for Clinical Research Project Assistant jobs? Cities near Normal, IL with the most Clinical Research Project Assistant job openings:
Clinical Research Project Assistant jobs near you
Sr. Clinical Research Associate, IQVIA

Sr. Clinical Research Associate, IQVIA

IQVIA

Bloomington, IL • On-site

$101K - $169K/yr

Full-time

Posted 28 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

56th of 210 rated it services

Job description

IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology, cardiovascular, renal, metabolic, CNS, Obesity (GLP-1), diabetes, GI, MASH/NASH, dermatology, or respiratory:

Job Overview:

Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Key Responsibilities:

Perform site monitoring visits (selection, initiation, monitoring, and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.

Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.

Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.

Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.

Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.

Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.

Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.

Collaborate and liaise with study team members for project execution support as appropriate. Responsibilities Essential Functions If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.

If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.

Qualifications:

Bachelor's Degree in scientific discipline or health care preferred.

Requires at least 2 years of year of on-site monitoring experience.

Equivalent combination of education, training and experience may be accepted in lieu of degree.

Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.

Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

Good therapeutic and protocol knowledge as provided in company training.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $101,600.00 - $169,300.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

What IQVIA employees say

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Benefits

Hours and flexibility

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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