Protocol deviations jobs

Manager Clinical Research Monitoring

OSF HealthCare · Posted May 29, 2026

Open

Peoria, Illinois, United States
Hybrid
Full-time · Manager
$43–$57 per hour

Manager Clinical Research Monitoring

OSF HealthCare · Posted May 29, 2026

Open

Peoria, Illinois, United States
Hybrid
Full-time · Manager
$43–$57 per hour

Clinical Research Monitor

OSF HealthCare · Posted May 28, 2026

Open

Peoria, Illinois, United States
Hybrid
Full-time
$39–$46 per hour
3+ years

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The Clinical Research Monitor performs monitoring and audit activities across OSF HealthCare’s research portfolio to support institutional oversight of active research studies.

Compensation

Expected pay for this position is $38.75 - $45.59/hour. Actual pay will be determined by experience, skills and internal equity. This is a Salaried position.

Responsibilities

Evaluates study conduct, regulatory documentation, and operational readiness to ensure compliance with protocols, regulatory requirements, and institutional policies.
Monitors and audits research studies.
Prepares monitoring reports and documentation of findings.
Collaborates with investigators, research teams, and clinical staff to support continuous quality improvement in research operations.

Requirements

Bachelor’s degree in healthcare, life sciences, nursing, public health, regulatory science, or related field.
Nice to have: Master’s degree in healthcare, life sciences, nursing, public health, regulatory science, or related field.
Nice to have: Clinical trial monitoring experience (CRA, sponsor monitor).
Nice to have: Industry-sponsored clinical trials experience.
Nice to have: Experience in large health system, academic medical center, or contract research organization (CRO).

Skills

Good Clinical Practice (GCP)

Sr. Clinical Operations Lead

Alimentiv · Posted Feb 19, 2026

Open

Boston, Massachusetts, United States
Senior
7–9 years

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Lead clinical operations oversight for regional and global trials, ensuring compliance and quality delivery across monitoring and site management activities.

Responsibilities

Provide regional and/or global clinical operations oversight across assigned studies
Lead and oversee Clinical Operations Leads (COLs) and CRAs
Oversee key monitoring and site management deliverables
Lead and support country and site feasibility, selection and start-up activities
Serve as a key liaison between monitoring team, Clinical Project Management, cross-functional study teams and Sponsors

Requirements

Bachelor’s degree in a relevant discipline
Nice to have: 10+ years of experience

Skills

clinical research CRA COL ICH-GCP clinical monitoring site management study start-up

Medical Monitor (Oncology)

PSI CRO · Posted Nov 5, 2026

Open

Munich, Bavaria, Germany
Full-time

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Provide medical oversight and expertise across global clinical trials in oncology, ensuring participant safety and compliance with GCP guidelines.

Responsibilities

Serve as primary medical point of contact for clinical trial sponsors, internal project teams, investigators and trial sites
Provide medical oversight throughout the conduct of clinical trials
Respond to medical questions from investigators, sites, sponsors, project teams, and third-party vendors
Provide medical input into eligibility assessments, protocol deviations, participant safety issues, and other trial-specific medical matters
Contribute medical expertise to clinical development plans, protocols, investigator brochures, informed consent documents, annual reports, clinical study reports, patient narratives, and scientific presentations

Requirements

Medical Doctor degree
Board certification in Oncology
Nice to have: Previous experience as a practicing Oncologist
Nice to have: Previous experience in clinical research or the pharmaceutical or CRO industry

Skills

Oncology Clinical research Pharmaceutical industry

Research Regulatory Coordinator

ECU Health Medical Center · Posted Nov 2, 2026

Open

Greenville, North Carolina, United States
Hybrid
Full-time · Entry
$59K–$87K per year
0–2 years

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Assist with daily regulatory maintenance and compliance of clinical research studies, manage study portfolio, support investigators and staff with regulatory activities, prepare required documents, maintain trackers and quality controls for informed consent, protocol deviations, amendments, and other essential regulatory functions.

Compensation

$59446.40 - $86646.56

Responsibilities

Assist with daily regulatory maintenance and compliance of clinical research studies
Manage a portfolio of studies within the enterprise
Support investigators, clinical and research staff with required regulatory activities
Prepare required documents and study records
Maintain trackers and quality controls for informed consent, protocol deviations, amendments

Requirements

Bachelor's Degree
Nice to have: science-related field

Skills

regulatory maintenance compliance regulatory workflows compliance auditing trackers quality controls

Manager Clinical Research Monitoring

Manager Clinical Research Monitoring

Compensation

Responsibilities

Requirements

Skills

Clinical Research Monitor

Compensation

Responsibilities

Requirements

Skills

Sr. Clinical Operations Lead

Responsibilities

Requirements

Skills

Medical Monitor (Oncology)

Responsibilities

Requirements

Skills

Research Regulatory Coordinator

Compensation

Responsibilities

Requirements

Skills

Benefits

Benefits