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Cras Jobs (NOW HIRING)

Fortrea

FSP - Sr. CRAs & CRA 1/2 - Ophthalmology

$110 - $145K/hr

Our FSP team is currently seeking experienced CRAs with Ophthalmology monitoring experience, major hub locations around the US will be considered. Regional travel with occasional outside travel at ...

Fortrea

FSP - Sr. CRAs & CRA 1/2 - Ophthalmology

OR · On-site +1

$110 - $145K/hr

Our FSP team is currently seeking experienced CRAs with Ophthalmology monitoring experience, major hub locations around the US will be considered. Regional travel with occasional outside travel at ...

Fortrea

Oncology - CAR-T - CRAs & Sr. CRAs - Remote US

OR · On-site +1

$105/hr

We are currently seeking Experienced Oncology CRAs to lead and support our Full Service Outsourcing team working with various sponsors. 1+ year of independent CRO/sponsor monitoring required. CAR-T ...

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Cras information

What is a 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.

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 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 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.

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What job categories do people searching Cras jobs look for?

The top searched job categories for Cras jobs are:

Cras jobs near you
Infographic showing various Cras job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 71% In-person, and 29% Remote job distribution.

CRAs & Sr. CRAs - Radiopharmaceutical Therapies - Remote US

Fortrea

Remote

$105/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 22 days ago

Fortrea rating

8.3

Company rating: 8.3 out of 10

Based on 11 frontline employees who took The Breakroom Quiz

29th of 75 rated research

Job description

We are currently seeking Experienced CRAs with Radiopharmaceutical therapeutic expertise to lead and support our Full Service Outsourcing team working with various sponsors. 1+ year of independent CRO/sponsor monitoring required. Open to major hub locations across the US. 60-70% travel, 8-10 DOS per month.
WHAT YOU WILL DO
You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency situations based upon clinical research standards.
Responsibilities:
  • Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -
  • Responsible for all aspects of site management as prescribed in the project plans
  • General On-Site Monitoring
  • Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study
  • Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements
  • Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data
  • Responsible for all aspects of registry management as prescribed in the project plans - Undertake feasibility work when requested
  • Complete Serious Adverse Event (SAE) reporting, process production of repo11s, narratives and follow up of SAEs
  • Independently perform CRF review; query generation and resolution against established data review guidelines on Fortrea or client data management systems as assigned by management
  • Assist with training of new employees, eg. co-monitoring
  • Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable) and may act as a local client contact as assigned
  • Perform other duties as assigned by management

Requirements
  • University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure)
  • 1+ years of Clinical Monitoring experience
  • Radiopharmaceutical experience is desired
  • Open to various hub locations

The important thing for us is you are comfortable working in an environment that is:
  • Fast paced: where no deviations from the study protocol are allowed, and not meeting a timeline for even few minutes will create a quality issue.
  • Changing priorities constantly asking you to prioritize and adapt on the spot.
  • Teamwork and people skills are essential for the study to run smoothly.
  • Technology based. We collect our data directly into an electronic environment.

What do you get?
Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including but not limited to:
  • Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers)
  • 401(K)
  • Paid time off (PTO) - Flex Plan
  • Employee recognition awards
  • Multiple ERG's (employee resource groups)
  • Target Pay Range (based on title): $105-145K

Work Environment:
  • Work is performed in an office environment with exposure to electrical office equipment.
  • Frequent travel to clients/ site locations with occasional travel both domestic and international.

Physical Requirements:
  • Ability to sit for extended periods and operate a vehicle safely.
  • Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.
  • Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
  • Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
  • Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
  • Regular and consistent attendance.
  • Varied hours may be required.

#LI - Remote
Applications will be accepted on an ongoing basis.
Learn more about our EEO & Accommodations request here.

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