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Clinical Monitoring Associate Jobs (NOW HIRING)

Syneoshealth

OR · On-site

Clinical Research Associate - Full-Service Syneos Health is a leading fully integrated ... Per the Clinical Monitoring/Site Management Plan (CMP/SMP): Assesses site processes. Conducts ...

WEP Clinical

Senior Clinical Research Associate

The WEP Clinical Senior Clinical Research Associate (Senior CRA) oversees all aspects of clinical ... They conduct on-site and remote monitoring to ensure protocol adherence, maintain essential ...

Vanguard Clinical

Clinical Research Associate (Pool)

CA · Remote

$90K - $130K/yr

Reporting to the Director - Clinical Monitoring, primarily responsible for the management of clinical sites and monitoring of clinical data at assigned sites. The Clinical Research Associate (CRA ...

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$12

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$55

How much do clinical monitoring associate jobs pay per hour?

As of Jul 1, 2026, the average hourly pay for clinical monitoring associate in the United States is $31.54, according to ZipRecruiter salary data. Most workers in this role earn between $21.15 and $41.59 per hour, depending on experience, location, and employer.

How does a Clinical Monitoring Associate typically collaborate with clinical research teams during a study?

Clinical Monitoring Associates (CMAs) work closely with clinical research teams, including Clinical Research Associates (CRAs), project managers, and site staff. They support the coordination of study activities by tracking site progress, preparing essential documentation, and helping resolve site queries. CMAs often participate in regular team meetings, communicate updates, and ensure accurate data collection and compliance with study protocols. This collaborative environment helps ensure that clinical trials run smoothly and meet regulatory requirements.

What are Clinical Monitoring Associates?

Clinical Monitoring Associates (CMAs) are professionals who support the conduct of clinical trials by assisting with the monitoring of study sites to ensure compliance with protocols, regulatory requirements, and good clinical practice guidelines. They work closely with Clinical Research Associates and study coordinators to track the progress of trials, verify data accuracy, and manage documentation. CMAs play a crucial role in maintaining data integrity and patient safety throughout the clinical research process.

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

To thrive as a Clinical Monitoring Associate, you need a background in life sciences, familiarity with Good Clinical Practice (GCP) guidelines, and a relevant bachelor's degree. Experience with clinical trial management systems (CTMS), electronic data capture (EDC), and certifications in clinical research (such as ACRP or SOCRA) are often required. Strong attention to detail, organizational skills, and effective communication help you excel in site management and ensure protocol adherence. These competencies are crucial for maintaining regulatory compliance, ensuring patient safety, and supporting the successful execution of clinical trials.
What cities are hiring for Clinical Monitoring Associate jobs? Cities with the most Clinical Monitoring Associate job openings:
What states have the most Clinical Monitoring Associate jobs? States with the most job openings for Clinical Monitoring Associate jobs include:
Clinical Monitoring Associate jobs near you
Infographic showing various Clinical Monitoring Associate job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 77% Full Time, 19% Part Time, and 3% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $65,604 per year, or $31.5 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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