Top 3 Clinical trial administrator Jobs in Naperville, Il

Clinical Trial Operations Consultant
Cloudbyz —Naperville, IL
- Full-time
- Nursing
- 7 years
- Master's degree
Clinical Trial Logistics Coordinator
MedSpeed —Elmhurst, IL
- $70,000 - $80,000 a year
- Full-time
- Background check
- Mid-level
- High school diploma or GED
- Health insurance
- Dental insurance
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13d
Senior Director, Global Head of Client Services - Clinical Trials Division
Thermo Fisher Scientific —Mount Prospect, IL
- $157,700 - $236,525 a year
- Full-time
- 11+ years
- Office
- Bachelor's degree
- Commuter assistance
- Paid parental leave

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Clinical Trial Operations Consultant
Cloudbyz —Naperville, IL
Bachelor’s or Master’s degree in Life Sciences, Nursing, Pharmacy, or related field. Experience with clinical trial management systems (CTMS), electronic data…
Clinical Research Coordinator
Northwestern Memorial Healthcare —Winfield, IL
Results are evaluated on a case-by-case basis, and we follow all local, state, and federal laws, including the Illinois Health Care Worker Background Check Act.
$28.55 - $41.40 an hour
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Clinical Trial Operations Consultant

Cloudbyz
Naperville, IL

Apply Now

Job Details

Full-time

Qualifications

Vendor relationship building
Drug regulation
ICH guidelines
Project management experience in healthcare
Managing projects
Clinical quality assurance standards
Research and development project management
Healthcare compliance
Cross-functional communication

Full Job Description

Position Summary:

We are seeking an experienced Clinical Trial Operations Consultant to provide strategic and hands-on support in the planning, execution, and oversight of clinical trials. The ideal candidate will possess strong project management skills, a deep understanding of clinical trial processes, and the ability to work cross-functionally with internal teams and external partners. This role is critical in ensuring operational excellence, regulatory compliance, and timely delivery of milestones across global clinical studies.

Key Responsibilities

Lead and manage the end-to-end execution of clinical trials (Phase I-IV), including study planning, start-up, conduct, and close-out activities.
Collaborate with cross-functional teams (Regulatory, Medical, Data Management, Quality, Safety, etc.) to align operational strategies with overall clinical development goals.
Develop, implement, and maintain project plans, timelines, risk management strategies, and trial budgets.
Monitor study performance metrics, track deliverables, and drive resolution of study issues to ensure quality and compliance.
Oversee vendor selection, contract negotiations, and performance management (CROs, labs, eClinical vendors, etc.).
Ensure trial conduct aligns with ICH-GCP, regulatory requirements, and SOPs.
Support the preparation of study documents, including protocols, investigator brochures, ICFs, study plans, and regulatory submissions.
Conduct feasibility assessments, site qualification, and initiation activities.
Provide leadership and mentorship to study teams, CRAs, and site monitors when applicable.
Contribute to process improvement initiatives and the development of clinical operations best practices.

Qualifications

Bachelor’s or Master’s degree in Life Sciences, Nursing, Pharmacy, or related field.
Minimum of 7+ years of experience in clinical trial operations and 3+ years in project/study management.
Proven track record of managing complex, global clinical studies across multiple therapeutic areas.
In-depth knowledge of ICH-GCP guidelines, FDA/EMA regulations, and industry best practices.
Experience with clinical trial management systems (CTMS), electronic data capture (EDC), eTMF, and other eClinical tools.
Strong organizational, analytical, and problem-solving skills.
Excellent interpersonal and communication skills, with the ability to influence cross-functional teams and vendors.
PMP or similar project management certification is a plus.
Experience working in a fast-paced, entrepreneurial environment or consulting role preferred.

Why Join Us

Engage with innovative and transformative clinical research programs
Work alongside passionate professionals committed to advancing healthcare
Flexible working arrangements and a collaborative, growth-oriented culture

Apply Now

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clinical trial administrator jobs in naperville, il

Clinical Trial Operations Consultant

Clinical Trial Logistics Coordinator

Senior Director, Global Head of Client Services - Clinical Trials Division

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I want to receive the latest job alert for clinical trial administrator in naperville, il

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