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Biomedical Project Manager Jobs in Springfield, IL

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Biomedical Project Manager information

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$21

$45

$75

How much do biomedical project manager jobs pay per hour?

As of Jun 5, 2026, the average hourly pay for biomedical project manager in Springfield, IL is $45.83, according to ZipRecruiter salary data. Most workers in this role earn between $39.81 and $50.29 per hour, depending on experience, location, and employer.

What is the difference between Biomedical Project Manager vs Biomedical Engineer?

AspectBiomedical Project ManagerBiomedical Engineer
Required CredentialsBachelor's or Master's in Biomedical Engineering, Project Management CertificationBachelor's or Master's in Biomedical Engineering or related field
Work EnvironmentProject teams, clinical settings, R&D departmentsLaboratories, manufacturing, clinical research
Employer & Industry UsageHospitals, biotech firms, medical device companiesMedical device companies, research institutions, hospitals

The Biomedical Project Manager focuses on overseeing projects, coordinating teams, and ensuring timely delivery of biomedical products. In contrast, the Biomedical Engineer is involved in designing, developing, and testing medical devices or systems. While both roles require biomedical engineering knowledge, the project manager emphasizes management skills and project execution, whereas the engineer concentrates on technical development and innovation.

What are Biomedical Project Managers?

Biomedical Project Managers are professionals responsible for overseeing and coordinating biomedical research projects, clinical trials, or product development within the healthcare or life sciences industry. They ensure that projects are completed on time, within budget, and in compliance with regulatory standards. Their role involves managing teams, communicating with stakeholders, and addressing potential risks or issues during the project lifecycle. Biomedical Project Managers often work closely with scientists, engineers, medical staff, and regulatory bodies to facilitate successful project outcomes.

How does a Biomedical Project Manager typically collaborate with cross-functional teams during a project lifecycle?

A Biomedical Project Manager works closely with diverse teams such as research scientists, regulatory specialists, engineers, and clinical staff to ensure project milestones are met. They facilitate communication across these groups by organizing regular meetings, tracking progress, and resolving issues that arise. This collaborative approach helps align project objectives, address challenges promptly, and maintain compliance with regulatory standards. Effective coordination and relationship-building are key to successfully delivering complex biomedical projects on time and within budget.

What are the key skills and qualifications needed to thrive as a Biomedical Project Manager, and why are they important?

To thrive as a Biomedical Project Manager, you need a solid background in biomedical sciences or engineering, project management experience, and often a relevant degree such as a BS/MS in a related field. Familiarity with project management software (e.g., MS Project, Asana), regulatory compliance systems (like FDA or ISO standards), and sometimes a PMP certification are typically important. Outstanding communication, leadership, and problem-solving skills help you coordinate cross-functional teams and manage stakeholder expectations. These competencies ensure successful project delivery, regulatory compliance, and effective collaboration in the complex biomedical industry.
What job categories do people searching Biomedical Project Manager jobs in Springfield, IL look for? The top searched job categories for Biomedical Project Manager jobs in Springfield, IL are:
What cities near Springfield, IL are hiring for Biomedical Project Manager jobs? Cities near Springfield, IL with the most Biomedical Project Manager job openings:
Biomedical Project Manager jobs near you
Infographic showing various Biomedical Project Manager job openings in Springfield, IL as of May 2026, with employment types broken down into 80% Full Time, 18% Part Time, and 2% Contract. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $95,329 per year, or $45.8 per hour.
Medical Reviewer/Safety Reviewer

Medical Reviewer/Safety Reviewer

Collabera

Springfield, IL • On-site

$40K - $65K/mo

Full-time

Posted 24 days ago

Job description

Join to apply for the Medical Reviewer/Safety Reviewer role at Collabera Join to apply for the Medical Reviewer/Safety Reviewer role at Collabera This range is provided by Collabera. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range $43.00/hr - $52.00/hr Direct message the job poster from Collabera This position is forMedical Reviewer/Safety Reviewer; This is 100% Remote Job Description: The Medical Device Safety team is a highly diverse department that plays a critical role in conceptualizing, designing, and implementing high-priority analytical strategies, clinical oversight, and initiatives.

The team is a high-profile high-impact team that works with PPS functions on a range of product initiatives. As a member of the team, you are at the forefront of working with leaders to identify critical priorities and drive high-value projects that make an impact on safety of our patients. Activities performed under this team: Assisting with ongoing continuous improvement projects spanning across departmental needs Responsible for individual and periodic medical device safety reporting Responsible for PI site notifications Providing support for training and automation efforts Support medical safety consultation activities in matters related to risk/benefit and proper product safety usage as needed.

Gain understanding of risk management regulations, standards, and guidance for medical devices and combination products. Biomedical engineer or RN Required Experience/Skills: Bachelor's degree in Nursing required or higher with minimum 3-4 years' experience in the medical device industry required Minimum 5 years direct patient care as a Registered Nurse preferred Expert level of understanding of global Medical Device regulations such as FDA, EU-MDR and other guidelines affecting device safety issues Sound understanding and application of device risk management and associated risk management documents such as Clinical Hazards List, Application Failure Mode and Effects Analysis, System Risk Analysis etc. Excellent critical thinking and application skills required Ability to speak up and support medical device safety analytics team in meetings and explain position of the clinical team Able to apply clinical knowledge and expertise to adverse event data and perform safety assessment Competent in ability to present device safety event data, orally and in writing Adheres to policies and regulations Must be Computer proficient (Windows, Word, Excel).

Responsibilities: Responsibilities include medical review, which involves in-house review of Case Report Forms (CRFs) including query resolution and addenda writing, QA of data listings. May manage the activities of regional contract CRAs, and organize the files and budgets associated with several clinical studies. Provides medical support which may include: Adverse Event Reporting - the investigation and reporting of medical product experiences, in depth investigation of medical adverse events and works with Medical Affairs, Clinical, and Regulatory Affairs in the preparation of documentation on adverse events for the FDA; or Medical Communication which includes writing standard and custom responses to communication requests, in-depth assistance to the medical and lay community by responding to inquiries with medical/scientific information that is more complex and requires more data than is supplied in the package insert or the standard letter database.

Off-label information would be disseminated at this level. May provide training internally and at investigator meetings on safety issues, responsible for serious adverse events and CRF completion, writing study summaries, and review protocols, study summary investigator brochures and IND annual updates for safety data verification. Pay Range: $45/hr to $52/hr (Without any benefits) Seniority level Seniority level Entry level Employment type Employment type Contract Job function Job function Administrative Referrals increase your chances of interviewing at Collabera by 2x Sign in to set job alerts for "Reviewer" roles.

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