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Cras Jobs (NOW HIRING)

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 ...

Lead CRAs work closely with US: Director of Clinical Monitoring, In-house CRAs, field CRAs, EU: Associate Director of Clinical Monitoring, CRAs, CTCs and Clinical Project Managers to ensure protocol ...

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Cras information

What are some common challenges faced by Cras professionals in their daily work, and how can they effectively overcome them?

Cras professionals often manage complex projects that require balancing multiple priorities and stakeholders. One common challenge is coordinating between different departments to ensure timelines and expectations are met, which requires strong communication and organizational skills. Additionally, adapting to rapidly changing industry trends may require continuous learning and flexibility. Building strong relationships with team members and staying updated with the latest industry tools can help Cras professionals navigate these challenges successfully.

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

I'm sorry, but 'Cras' does not appear to be a recognized real-world professional occupation, so I cannot provide a relevant answer.

What is the difference between Cras vs Network Administrators?

AspectCrasNetwork Administrators
Required CredentialsTypically certifications like CompTIA A+ or Cisco CCNASame certifications, often with additional specialization
Work EnvironmentData centers, server rooms, IT departmentsOffice settings, server rooms, remote support
Industry UsageIT, telecommunications, data managementIT, corporate, government sectors
Common Search IntentUnderstanding roles, job requirements, career pathSimilar roles, job comparison, qualifications

Both Cras and Network Administrators share similar credentials and work environments, often overlapping in IT and data management sectors. While Cras may focus more on specific data or system management tasks, Network Administrators typically handle network infrastructure and security. They are frequently searched together due to their related responsibilities and industry usage, making them comparable career options in the IT field.

What are Cras?

The term 'Cras' does not correspond to a recognized job title in most industries. It may be a typographical error or an abbreviation that requires clarification. If you meant 'CRAs,' it could refer to Clinical Research Associates, professionals who monitor clinical trials and ensure compliance with regulatory standards. Please provide additional context or check the spelling to get more accurate information about the role you are interested in.
More about Cras jobs
Infographic showing various Cras job openings in the United States as of May 2026, with employment types broken down into 98% Full Time, 1% Part Time, and 1% Contract. Highlights an 74% Physical, 2% Hybrid, and 24% Remote job distribution.
Clinical Research Associate

Clinical Research Associate

Alira Health

San Francisco, CA

Full-time

Posted 3 days ago


Job description

Join our global team dedicated to innovation and initiative, where physical walls and different time zones don't limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is driven by our shared values: be courageous, be accountable, be honest, be inclusive and elevate others.

Job Description Summary

Job Description

ROLE

The Clinical Research Associate is an important member of the Alira Health Clinical team. CRAs are highly motivated and function independently to conduct site monitoring responsibilities for clinical trials. CRAs work closely with the In-house CRAs, Lead CRAs, Director of Clinical Monitoring and Project Managers to ensure sites' protocol compliance, address site questions, and assist with study recruitment, site training, and other site-related issues.

KEY RESPONSABILITIES
  • Performs qualification, initiation, interim, and close-out visits and ensures proper documentation of site visits.

  • Prepares consistently accurate and timely monitoring visit reports documenting site-related problems, resolutions, actions taken, protocol deviations, study progress, and enrollment status.

  • Facilitates adverse event reporting and ensures the reconciliation of SAE reports with source documentation and CRFs.

  • Ensures integrity of CRF data through meticulous and thorough source document review and verification.

  • Conducts investigational product accountability.

  • Reviews regulatory binder for required documents.

  • Works closely with in-house CRAs and data management to resolve queries on discrepant data.

  • Proactively identifies site issues and develops problem-solving strategies for sites.

  • Maintains regular contact with study sites to ensure protocol/GCP compliance, assesses patient accrual rates, and responds to sponsor requests.

  • Conducts audit preparation at study sites as needed.

  • Works with other CRAs to maintain consistency and promote a collaborative team atmosphere.

  • Manages and resolves conflicting priorities to deliver on commitments.

  • Complies with ICH GCP guidelines, FDA regulations, and company SOPs.

  • Participates in industry and client meetings.

  • Performs additional duties as assigned.

DESIRED QUALIFICATION & EXPERIENCE
  • BS/BA from an undergraduate program or equivalent experience

  • 2 years of clinical research experience

TECHNICAL COMPETENCES & SOFT SKILLS
  • Ability to travel.

  • Proven ability to be careful, thorough, and detail-oriented.

  • Strong organizational skills and the ability to multi-task and work effectively in a fast-paced environment.

  • Self-starter who thrives in a collaborative, yet less structured team environment

  • Ability to problem-solve unstructured or ambiguous challenges.

  • Strong command of English, both written and verbal.

  • Excellent communication and interpersonal skills with customer service orientation.

  • Proficient with MS Office Suite, particularly Word and Excel.

  • Permanent authorization to work in the country where you are applying.

Languages

English

Education

Bachelor of Science (BS): Biology, Bachelor of Science (BS): Life Sciences

Contract Type

Regular