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Clinical Monitoring Jobs (NOW HIRING)

Novotech

$170K - $200K/yr

About the Role The Director Centralized Clinical Monitoring is a senior leadership role responsible for the strategic and operational oversight of Risk-Based Quality Management (RBQM) and centralized ...

West Virginia University Health System

$19.50 - $25.25/hr

The Clinical Monitoring Technician plays a key role in supporting the safe and efficient use of cardiac monitoring equipment throughout the hospital. This position is responsible for assisting with ...

RDI

Clinical Monitoring Standards Lead

Los Angeles, CA · On-site +1

You will also help modernize clinical trial monitoring as the industry moves toward risk-based monitoring, real-time oversight, remote-first execution, and AI-assisted workflows without compromising ...

RDI

Clinical Monitoring Standards Lead

Los Angeles, CA · On-site

You will also help modernize clinical trial monitoring as the industry moves toward risk-based monitoring, real-time oversight, remote-first execution, and AI-assisted workflows without compromising ...

RDI

Clinical Monitoring Standards Lead

Los Angeles, CA · On-site

You will also help modernize clinical trial monitoring as the industry moves toward risk-based monitoring, real-time oversight, remote-first execution, and AI-assisted workflows without compromising ...

Alimentiv

Director, Clinical Trial Management

Chicago, IL · Remote

$81K - $111K/yr

Working in conjunction with clinical monitoring and project leadership team members, identify, develop, plan for, monitor, approve and/or report on project specific processes and services related to ...

Alimentiv

Director, Clinical Trial Management

Philadelphia, PA · On-site +1

$80K - $110K/yr

Working in conjunction with clinical monitoring and project leadership team members, identify, develop, plan for, monitor, approve and/or report on project specific processes and services related to ...

Alimentiv

Director, Clinical Trial Management

Raleigh, NC · Remote

$81K - $111K/yr

Working in conjunction with clinical monitoring and project leadership team members, identify, develop, plan for, monitor, approve and/or report on project specific processes and services related to ...

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Clinical Monitoring information

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$12

$41

$69

How much do clinical monitoring jobs pay per hour?

As of Jul 1, 2026, the average hourly pay for clinical monitoring in the United States is $41.13, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $52.64 per hour, depending on experience, location, and employer.

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

To thrive in Clinical Monitoring, you need a solid background in life sciences or nursing, strong knowledge of clinical trial protocols, and often a relevant degree such as a BS in a scientific field. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and certifications like ACRP or SOCRA are highly valued. Exceptional attention to detail, strong organizational skills, and effective communication are crucial soft skills for managing trial sites and ensuring compliance. These competencies are vital for ensuring data integrity, regulatory adherence, and the smooth progress of clinical trials.

What is the difference between Clinical Monitoring vs Clinical Data Management?

AspectClinical MonitoringClinical Data Management
Primary RoleOversees site activities, ensures protocol adherence, monitors patient safetyCollects, validates, and manages clinical trial data
Required CredentialsTypically a degree in life sciences, nursing, or related field; often requires monitoring certificationsDegree in life sciences, biostatistics, or related; data management certifications beneficial
Work EnvironmentOn-site at clinical trial sites or remotely, interacting with site staffPrimarily office-based, working with electronic data capture systems
Industry UsageCommonly used in clinical trial phases, especially during site visitsUsed throughout the trial for data collection, cleaning, and analysis

Clinical Monitoring focuses on overseeing clinical trial sites and ensuring compliance, while Clinical Data Management handles the collection and validation of trial data. Both roles are essential in clinical research, often working closely but with distinct responsibilities.

What is clinical monitoring?

Clinical monitoring is the process of overseeing clinical trials to ensure they are conducted, recorded, and reported in accordance with the protocol, standard operating procedures, Good Clinical Practice (GCP), and regulatory requirements. Clinical monitors, often called Clinical Research Associates (CRAs), are responsible for checking the progress of a clinical trial at research sites, verifying data accuracy, ensuring participant safety, and ensuring compliance with regulations. Their work is essential in maintaining the integrity of clinical data and the safety of trial participants.

What are some common challenges faced by professionals in Clinical Monitoring, and how can they be addressed?

Clinical Monitoring professionals often encounter challenges such as managing multiple study sites, ensuring protocol compliance, and maintaining clear communication with site staff. Navigating regulatory requirements and handling unexpected issues, like protocol deviations or data discrepancies, can also be demanding. To address these, strong organizational skills, proactive communication, and thorough documentation are essential. Building collaborative relationships with site personnel and staying updated on regulatory guidelines can help ensure smoother study progress and data integrity.
More about Clinical Monitoring jobs
What cities are hiring for Clinical Monitoring jobs? Cities with the most Clinical Monitoring job openings:
What are the most commonly searched types of Clinical Monitoring jobs? The most popular types of Clinical Monitoring jobs are:
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Clinical Monitoring jobs near you
Infographic showing various Clinical Monitoring job openings in the United States as of June 2026, with employment types broken down into 89% Full Time, 7% Part Time, and 4% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $85,542 per year, or $41.1 per hour.
Associate Manager, Clinical Monitoring

Associate Manager, Clinical Monitoring

Crinetics Pharmaceuticals

Remote

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 7 days ago

Job description

Position Summary:
The Associate Manager, Clinical Monitoring supports global and regional clinical trial operations (CTO) and Clinical Monitoring management in the conduct and oversight of clinical site management and monitoring activities performed by Crinetics or an outsourcing partner. This role may conduct Clinical Monitoring visits for assigned Crinetics studies. The Associate Manager may support the development of processes, procedures, and tools/templates related to monitoring and site management activities.
Essential Job Functions and Responsibilities:
These may include but are not limited to:
  • With direction from CTO or Clinical Monitoring management, implement strategy for in-house, regional monitoring activities on assigned studies applying a risk-based approach when indicated.
  • Lead monitoring activities on assigned studies. This can include review of protocols, CRFs and completion guidelines, study manuals and other related documents.
  • Author or review Clinical Monitoring Plan in collaboration with CTO and ensure CRA compliance to current plan.
  • Manage the CRA monitoring visit schedule for each assigned study ensuring visit frequency and scheduled time on site aligns with risk-based indicators and site metrics.
  • Review and finalize visit reports for regional CRAs managed by Crinetics according to study timelines. Follow up with CRAs regarding outstanding trip reports and follow-up letters.
  • Track status of action items and queries.
  • Maintain, and/or act on metrics related to CRA performance or site status.
  • Support CRAs and CTO with the implementation of site corrective actions related to issues identified during monitoring activities.
  • Track and report to study team and leaders on compliance, trends and metrics related to monitoring and site management.
  • Support TMF set-up, maintenance, ongoing quality review, and final reconciliation of study documents as needed.
  • With direction from CTO or Clinical Monitoring management, manage the monitoring oversight strategy, including risk-based approaches, to assess the quality and compliance of CRO or FSP partners on assigned studies.
  • Manage or conduct monitoring oversight visits (MOVs) with CRO CRAs to assess compliance to the protocol and Clinical Monitoring Plan and document results of the visit.
  • Review monitoring visit reports from CRO CRAs and escalate monitoring trends or findings to CTO and Clinical Monitoring management.
  • Conduct or participate in Clinical Monitoring visits for Crinetics studies.
  • Mentors and provides leadership and direction to the CRA team members on study related questions from start-up through closure.
  • Ensure adequate resourcing for CRAs on assigned Crinetics studies; work with CTO to plan for CRA re-assignment or acquisition of additional resources.
  • Escalates any study-related issues or impacts on deliverables, as appropriate, to the Clinical Monitoring management.
  • Support CRAs, study team, and Quality with responses to audits or inspections.
  • May provide feedback and assist with the development of departmental policies and procedures toward increased efficiency and quality of deliverables. May contribute to the development of SOPs and other procedural documents.
  • May conduct monitoring assessment or FSP oversight visits as needed.
  • Support development and manage Clinical Monitoring budget requirements for assigned studies.
  • Other duties as assigned.

Education and Experience:
Required:
  • BS in biological sciences or related discipline with at least 5 years of experience working in the biotechnology/pharmaceutical industry. Experience in endocrine disorders preferred.
  • Monitoring experience in startup, execution and close out activities related to clinical studies; experience using risk-based monitoring processes strongly preferred.
  • Previous experience as a Lead CRA, Trial Manager, or equivalent strongly preferred.
  • Demonstrates critical thinking, root cause analysis and problem solving to support CRAs with identifying site process failures; assist CRAs to develop corrective and preventative actions to bring sites into compliance.
  • An understanding and demonstrated application of Good Clinical Practices, ICH Guidelines and regulatory requirements. Able to comply with safety standards and respect privacy and confidentiality.
  • In-depth experience with cross functional drug development with prior regulatory inspection experience preferred.
  • Excellent writing skills as they relate to the preparation of clinical trial documents.
  • Excellent interpersonal skills with strong oral/written communication and presentation skills
  • Excellent negotiation skills and a tactful approach that leads to high value on services obtained and outcomes achieved.
  • Demonstrated leadership skills.
  • Good judge of risks and a keen ability to analyze options and manage outcomes.
  • Well-versed with the latest trends in the clinical trial industry

Physical Demands and Work Environment:
Physical Activities: On a continuous basis, sit at desk for a long period of time; intermittently answer telephone and write or use a keyboard to communicate through written means. Some walking and lifting up to 25 lbs. may be required. The noise level in the work environment is typically low to moderate. The physical demands described above are representative of those that must be met by an employee to successfully perform the essential functions and responsibilities of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions and responsibilities.
Laboratory Activities (if applicable): Biology and chemical laboratory environment experience needed. Environmental health and safety requirements also apply.
Travel:
You may be required to travel for up to 5% of your time.
Equal Opportunity Employer:
Crinetics is proud to be an Equal Opportunity Employer. We provide equal employment opportunities to all employees and employment applicants without regard to unlawful considerations of sex, sexual orientation, gender (including gender identity and/or expression), pregnancy, race, color, creed, national or ethnic origin, citizenship status, religion or similar philosophical beliefs, disability, marital and civil union status, age, genetic information, veteran status or any personal attribute or characteristic that is protected by applicable local, state or federal laws.
Salary Range
The salary range for this position is: $115,000 - $144,000.
In addition to your base pay, our total rewards program consists of a discretionary annual target bonus, stock options, ESPP, and 401k match. We also provide top-notch health insurance plans for employees (and their families) to include medical, dental, vision and basic life insurance, 20 days of PTO, 10 paid holidays, and a winter company shutdown.

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