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Clinical Trials Jobs in Springfield, IL (NOW HIRING)

Springfield Clinic

Oncology Research Liaison

Springfield, IL · On-site

$24 - $32/hr

Coordinate startup and ongoing management of IRB-approved clinical trials in compliance with federal, state, and institutional requirements (ICH/GCP, OSHA, IATA). * Establish relationships with trial ...

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The Medicus Firm

Psychiatry Physician

Springfield, IL

$400K/yr

Build the academic psychiatry career you actually want - a flexible blend of outpatient care, consults, teaching, and the freedom to incorporate ECT, TMS, telepsychiatry, clinical trials, or research ...

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$95

How much do clinical trials jobs pay per hour?

As of Jul 31, 2026, the average hourly pay for clinical trials in Springfield, IL is $61.96, according to ZipRecruiter salary data. Most workers in this role earn between $50.29 and $69.81 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Clinical Trials position, and why are they important?

To thrive in Clinical Trials roles, you need a strong understanding of clinical research principles, Good Clinical Practice (GCP) guidelines, and a background in life sciences or healthcare. Familiarity with electronic data capture (EDC) systems, regulatory compliance software, and relevant certifications such as GCP or CCRA is highly valuable. Attention to detail, organizational skills, and effective communication enable collaboration across multidisciplinary teams. These competencies are crucial for ensuring protocol adherence, data integrity, and the successful execution of trial activities.

How to get into clinical trial work?

To work in clinical trials, individuals typically need a background in healthcare, life sciences, or related fields, along with relevant certifications such as Good Clinical Practice (GCP). Entry-level roles often require strong organizational skills, attention to detail, and familiarity with regulatory requirements; some positions may also require a bachelor's degree or higher. Gaining experience through internships or training programs can improve job prospects in this field.

How much money can I make doing clinical trials?

Clinical trial participants can earn anywhere from $50 to several thousand dollars depending on the study's duration, complexity, and requirements. Compensation varies based on factors such as the type of trial, location, and whether medical procedures or tests are involved. Participants often receive payment after completing the study or specific milestones within it.

Which clinical trials pay the most?

Clinical trials involving high-risk or complex treatments, such as oncology or rare disease studies, often offer higher compensation to participants and staff. Additionally, roles like clinical research coordinators or principal investigators in well-funded trials tend to earn more due to their responsibilities and expertise. Compensation varies based on trial phase, location, and the level of experience required.

What are some common career paths or advancement opportunities for professionals working in Clinical Trials?

Many professionals in Clinical Trials start their careers as Clinical Research Coordinators, Clinical Research Associates, or Data Managers. With experience, you can advance to roles such as Senior Clinical Research Associate, Clinical Trial Manager, or Project Manager, and potentially move into areas like regulatory affairs, medical writing, or quality assurance. The role offers continuous learning opportunities, exposure to innovative therapies, and often provides the chance to lead larger, more complex studies as you progress. Advancement is typically supported by additional certifications, strong performance, and a proactive approach to professional development. Teamwork and networking within the industry can also open new doors for growth.

Are clinical trial jobs in high demand?

Clinical trial jobs are in high demand due to the ongoing need for new medical treatments and the growth of the healthcare industry. Positions such as clinical research coordinators and data managers are often sought after, especially for those with relevant certifications and experience in regulatory compliance and data management tools.

What is a Clinical Trials job?

A Clinical Trials job involves managing, coordinating, or supporting research studies that evaluate the safety and effectiveness of medical treatments, drugs, or devices. Professionals in this field work on trial design, patient recruitment, data collection, regulatory compliance, and reporting results. Roles can range from clinical research coordinators to trial managers and regulatory specialists. The goal is to ensure that studies follow ethical guidelines and produce reliable data for medical advancements.

What are popular job titles related to Clinical Trials jobs in Springfield, IL? For Clinical Trials jobs in Springfield, IL, the most frequently searched job titles are:
What job categories do people searching Clinical Trials jobs in Springfield, IL look for? The top searched job categories for Clinical Trials jobs in Springfield, IL are:
What cities near Springfield, IL are hiring for Clinical Trials jobs? Cities near Springfield, IL with the most Clinical Trials job openings:
Clinical Trials jobs near you
Infographic showing various Clinical Trials job openings in Springfield, IL as of July 2026, with employment types broken down into 2% As Needed, 70% Full Time, 22% Part Time, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $128,878 per year, or $62 per hour.

Oncology Research Liaison

Springfield Clinic

Springfield, IL • On-site

$24 - $32/hr

Other

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

Springfield Clinic rating

6.7

Company rating: 6.7 out of 10

Based on 58 frontline employees who took The Breakroom Quiz

529th of 885 rated healthcare providers

Job description

The Oncology Liaison serves as a key connector between clinical operations, oncology providers, and research initiatives at Springfield Clinic (SC). This role supports the growth and coordination of oncology-related programs, including clinical research, by facilitating communication, identifying opportunities, and ensuring efficient execution of approved protocols.

The Oncology Liaison partners closely with investigators, clinical staff, and external sponsors to advance program development, improve patient access to research, and ensure compliance with regulatory standards.

Job Relationships

Reports to the Cancer Center Director

Maintains a dotted-line reporting relationship to Clinical Research Leadership

Principal Responsibilities

  • Serve as the primary liaison for oncology-related research and program initiatives across Springfield Clinic.
  • Identify program growth opportunities, including feasibility assessment for new clinical trials and partnerships.
  • Coordinate startup and ongoing management of IRB-approved clinical trials in compliance with federal, state, and institutional requirements (ICH/GCP, OSHA, IATA).
  • Establish relationships with trial sponsors and Contract Research Organizations (CRO's) to facilitate expansion of drug pipelines and clinical trial opportunities.
  • Facilitate communication between investigators, clinic staff, sponsors, and the Clinical Research Department.
  • Educate providers and staff on study protocols, amendments, and research-related requirements to ensure adherence and engagement.
  • Maintain oversite of accurate and complete study documentation, including source documentation, case report forms, and investigational product accountability.
  • Collaborate with Clinical Research Associates (CRAs) and study monitors to ensure data accuracy, resolve discrepancies, and maintain audit readiness. This coordination and collaboration could include:
  • Screen, consent, and enroll eligible patients into clinical trials; ensure appropriate follow-up through study completion.
  • Conduct study visits per protocol and oversee collection, processing, and shipment of specimens in compliance with regulatory standards.
  • Monitor research patients for adverse events and ensure timely reporting of serious adverse events (SAEs) and protocol deviations.
  • Support onboarding, education, and development of staff involved in oncology research activities.
  • Participate in financial oversight of oncology research and program operations, including contributing to budget development, monitoring expenses, and ensuring appropriate utilization of resources aligned with program goals.
  • Ensure compliance with Springfield Clinic policies, including incident reporting, privacy (HIPAA), and code of conduct standards.
  • Maintain required certifications and hospital privileges as applicable.
  • Comply with the Springfield Clinic incident reporting policy and procedures.
  • Adhere to all OSHA and Springfield Clinic training & accomplishments as required per policy.
  • Provide excellent customer service and adhere to Springfield Clinic's Code of Conduct and Ethics Standards.

  • Perform other job duties as assigned.

Education/Experience

  • Bachelor's degree in Nursing or a related healthcare field required.
  • Minimum of 3-5 years of clinical oncology and/or research experience required.
  • Prior clinical research experience is strongly preferred.

Licenses/Certificates

  • CPR certification (American Heart Association) preferred within 30 days of hire.
  • Research certification (CCRP or CCRC) encouraged within two (2) years of employment.

Knowledge, Skills and Abilities

  • Strong knowledge of clinical research regulations (ICH/GCP, CFR, HIPAA).
  • Proficiency in EMR systems, Microsoft Office, and sponsor-required platforms.
  • Excellent organizational, communication, and interpersonal skills.
  • Ability to effectively collaborate with physicians, staff, sponsors, and patients.
  • Strong problem-solving and critical-thinking abilities.
  • Ability to work independently and manage multiple priorities.
  • High attention to detail and commitment to compliance.

Working Environment

  • Primarily office-based with travel to clinic locations as needed.

PHI/Privacy Level

HIPAA1

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