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Temp Cra Monitor Jobs (NOW HIRING)

Alimentiv

Sr. Clinical Operations Lead

Raleigh, NC

May be required to manage/oversee investigator sites including CRA responsibilities, on a temporary or permanent basis. Project Liaison * Conduct regular global CRA calls with the monitoring and site ...

Alimentiv

Sr. Clinical Operations Lead

Boston, MA · Remote

May be required to manage/oversee investigator sites including CRA responsibilities, on a temporary or permanent basis. Project Liaison * Conduct regular global CRA calls with the monitoring and site ...

Alimentiv

Sr. Clinical Operations Lead

Newark, NJ · Remote

May be required to manage/oversee investigator sites including CRA responsibilities, on a temporary or permanent basis. Project Liaison * Conduct regular global CRA calls with the monitoring and site ...

Alimentiv

Sr. Clinical Operations Lead

Raleigh, NC · Remote

May be required to manage/oversee investigator sites including CRA responsibilities, on a temporary or permanent basis. Project Liaison * Conduct regular global CRA calls with the monitoring and site ...

KBRA

ABS Equipment - Director (NY / Chicago)

New York, NY · Hybrid

$160K - $190K/yr

Surveil and monitor rated transactions and update existing ratings as warranted. * Attend and ... CRA with the UK Financial Conduct Authority pursuant to the Temporary Registration Regime. In ...

KBRA

Corporates - Senior Analyst (Chicago)

Chicago, IL · Hybrid

$85K - $100K/yr

... investors and monitor a wide variety of companies within our growing Corporate Finance rating ... CRA with the UK Financial Conduct Authority pursuant to the Temporary Registration Regime. In ...

KBRA

ABS Equipment - Director (NY / Chicago)

New York, NY · On-site

$160K - $190K/yr

Surveil and monitor rated transactions and update existing ratings as warranted. * Attend and ... CRA with the UK Financial Conduct Authority pursuant to the Temporary Registration Regime. In ...

KBRA

ABS Consumer - Director (NY/ Chicago)

New York, NY · Hybrid

$160K - $190K/yr

Surveil and monitor outstanding transactions, updating ratings as warranted. * Attend and lead ... CRA with the UK Financial Conduct Authority pursuant to the Temporary Registration Regime. In ...

KBRA

ABS Consumer - Director (NY/ Chicago)

New York, NY · On-site

$160K - $190K/yr

Surveil and monitor outstanding transactions, updating ratings as warranted. * Attend and lead ... CRA with the UK Financial Conduct Authority pursuant to the Temporary Registration Regime. In ...

KBRA

CMBS Surveillance - Analyst (PA)

Dresher, PA · Hybrid

$65K - $75K/yr

Our commercial real estate credit ratings team monitors a book of over $470 billion transactions ... CRA with the UK Financial Conduct Authority pursuant to the Temporary Registration Regime. In ...

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All JobsTemp Cra Monitor Jobs

Temp Cra Monitor information

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$11K

$79.4K

$137.5K

How much do temp cra monitor jobs pay per year?

As of Jun 3, 2026, the average yearly pay for temp cra monitor in the United States is $79,437.00, according to ZipRecruiter salary data. Most workers in this role earn between $33,000.00 and $136,500.00 per year, depending on experience, location, and employer.

What is the difference between Temp Cra Monitor vs Temp Cra Coordinator?

AspectTemp Cra MonitorTemp Cra Coordinator
CertificationsTypically requires clinical research certifications or relevant experienceOften requires similar certifications, with additional project management skills
Work EnvironmentWorks in clinical settings, monitoring trial progressCoordinates activities across teams, often in office or clinical settings
Employer & Industry UsageUsed in pharmaceutical and biotech industries for trial oversightUsed in similar industries for managing clinical trial operations

The Temp Cra Monitor primarily focuses on overseeing clinical trial activities and ensuring compliance, while the Temp Cra Coordinator handles the organization and coordination of trial processes. Both roles require similar certifications and work in comparable environments, but their responsibilities differ in scope and focus.

More about Temp Cra Monitor jobs
What cities are hiring for Temp Cra Monitor jobs? Cities with the most Temp Cra Monitor job openings:
What are the most commonly searched types of Cra Monitor jobs? The most popular types of Cra Monitor jobs are:
What states have the most Temp Cra Monitor jobs? States with the most job openings for Temp Cra Monitor jobs include:
What job categories do people searching Temp Cra Monitor jobs look for? The top searched job categories for Temp Cra Monitor jobs are:
Temp Cra Monitor jobs near you
Infographic showing various Temp Cra Monitor job openings in the United States as of May 2026, with employment types broken down into 83% Full Time, and 17% Temporary. Highlights an 83% In-person, and 17% Remote job distribution, with an average salary of $79,437 per year, or $38.2 per hour.

Sr. Clinical Operations Lead

Alimentiv

Raleigh, NC

Full-time

Posted 14 days ago

Job description

Responsible for the clinical operations of a project within a defined regional/global level.  Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and Investigator sites in accordance with the Monitoring Plan, Protocol, Good Clinical Practice (GCP), ICH guidelines and local regulations.  The COL acts as a primary liaison between the CRAs and the clinical project team.  Additional responsibilities include project specific training of CRAs, conducting assessment visits with CRAs, implementation of enrollment and recruitment strategies, preparation of the monitoring plan and other structural documentation and the oversight of monitoring visit scheduling, site and monitoring performance metrics, issue escalation and corrective actions.  The COL will develop study tools for site and CRA use, review visit reports, review and track protocol deviations, and support other objectives for clinical operations and the clinical project team.
Project Oversight
  • Overall oversight of (a group of) regional CRAs to ensure (site) compliance with study protocol, study plans, ICH-GCP, local regulations and study timelines.
  • Monitoring support visits (Co-monitoring), per project requirements, to aid the site/CRA in the satisfactory performance and compliance with standards mentioned above.
  • May support clinical project team by providing oversight of study deliverables related to other departments (e.g. Data Management, TMF Operations, etc.)
  • Oversee regional startup and feasibility activities.
  • Assist in vendor management activities as required per project.
  • Perform review of visit reports for quality, compliance and appropriate site management.
  • Assure compliance with high quality and timely project deliverables according to the project requirements and the monitoring plan.
  • Proactive management of site and country performance (recruitment, data collection, document collection, TMF review etc.) and inform clinical project team on progress.
  • Contribute to financial project management processes as applicable.  May include but may not be limited to input on revenue recognition, site payments, and site pass-through expense review.
  • May be required to manage/oversee investigator sites including CRA responsibilities, on a temporary or permanent basis.         
Project Liaison
  • Conduct regular global CRA calls with the monitoring and site management team, as well as individual/country CRA calls 
  • Attend meetings with Study Sponsor to provide status updates on country and site progress
  • Provide operational support and guidance to the monitoring team throughout project.
  • Provide project training/mentoring to regional CRAs on study procedures, clinical plans and guidelines, and timelines for the study. Ensures study specific training requirements are completed and documented.
  • First point of contact for regional CRAs for study-specific questions and issues. Escalates to PM and other functions as appropriate.
  • Support line managers by providing status updates on utilization and performance of CRAs. 
  • Liaise with line manager for assigning sites to CRAs following line manager allocation of a CRA resource to the project. 
  • Conduct CRA Assessment visits per departmental requirements to assess the performance of the CRA against their monitoring responsibilities.
Study Documents and Plans
  • Develop training materials and study tools for sites and CRAs, including monitoring plans.
  • Develop and implement enrolment and recruitment strategies together with clinical project team.
  • Develop presentation materials for and presents at Sponsor Kickoff meetings, Investigator meetings and Sponsor Calls (as needed), and prepares presentations for Site Qualification Visits and Site Initiation Visits.
 
Qualifications
  • College diploma/degree AND 7-9 years related experience +continuous training and knowledge/skills upgrading
OR
  • Undergraduate university degree (Bachelors or Honors Bachelors) AND 4-6 years' experience + substantial on-going job-related training
Other
  • Health Sciences, Life Sciences or Nursing specialty preferred, or SoCRA and/or ACRP Certification/Designation.
  • Should have a minimum of 3 years CRA experience, have strong experience with EDC systems, be proficient with MS Office, have strong written and verbal communication skills and highly effective interpersonal and organizational skills.
  • Demonstrate the following attributes: proactive, detail oriented, task-driven and highly organized.
  • Demonstrate the critical elements of GCPs and local regulations as they relate to clinical monitoring, IRB/EC and Investigator responsibilities.
  • Demonstrated ability in report writing and strong ability to critically understand clinical research documents.
  • Ability to handle multiple tasks to meet deadlines in a dynamic environment. 
 
Working Conditions
  • Home-based
$86,000 - $143,000 a year
+ Bonus
Accommodations for persons with disabilities are available on request in respect of all aspects of the recruitment and selection lifecycle. Requests can be directed to [email protected]
 
PHISHING SCAM WARNING: Alimentiv is aware of the continued increase of phishing scams, leveraging various methods of attack via email, text, voice and social media. Please note that Alimentiv only uses company email addresses, which contain "@alimentiv.com", to communicate with candidates via email. If you are contacted by someone about an open job at Alimentiv, please verify the domain of the sender's email address and that they are asking you to apply on this website. If you believe you've been a victim of a phishing scam, please contact your local government cyber authority to report.
 
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