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Permanent In House Cra Jobs in Oregon (NOW HIRING)

Fortrea

Experienced CRA 2

OR · On-site +1

$105/hr

We are currently seeking experienced CRA 2s to lead and support our Full Service Outsourcing team ... Ability to access and use a variety of computer software developed both in-house and off-the-shelf.

Fortrea

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

OR · On-site +1

$110 - $145K/hr

Seeking Sr. CRA level and CRA 1s and 2s (1-2 years of monitoring). WHAT YOU WILL DO You will ... Ability to access and use a variety of computer software developed both in-house and off-the-shelf.

Fortrea

Sr. CRA 2, FSP - Invitro Diagnostics

OR · On-site +1

$125 - $140K/hr

Our FSP team is currently seeking Sr. CRA 2s with 4+ years of monitoring residing in the East Coast ... Ability to access and use a variety of computer software developed both in-house and off-the-shelf.

Fortrea

Sr. CRA 2, FSP - Oncology - West Coast

OR · On-site +1

$115 - $140K/hr

Our FSP team is currently seeking a Sr. CRA 2 with 4+ years of monitoring as well as strong ... Ability to access and use a variety of computer software developed both in-house and off-the-shelf.

Salem Clinic PC

Physician OB/GYN

Salem, OR · On-site

Salem Clinic is looking for an Obstetrician-Gynecologist to join our team! * Full-time permanent ... OB hospitalists and in house dedicated OB anesthesia at Salem Hospital (level III NICU) * Must work ...

Salem Clinic PC

Endocrinologist

Keizer, OR · On-site

... permanent * Board Certified * Salaried; quarterly production bonus eligible * 4.5-day work week ... From in-house tech support to in-house maintenance and administrative staff, we have your needs ...

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Permanent In House Cra information

What is a permanent in house CRA?

A Permanent In House CRA (Clinical Research Associate) is a professional who monitors clinical trials from within the sponsor or CRO’s office rather than traveling to investigator sites. They are responsible for supporting the management and oversight of clinical studies, ensuring compliance with protocols, regulatory requirements, and data integrity. Unlike field-based CRAs, In House CRAs typically handle documentation, query resolution, and site communication remotely. These roles are usually full-time, long-term positions within a company, offering job stability and opportunities for career growth.

What skills and qualifications are needed to thrive as a permanent in house CRA?

To excel as a Permanent In-House CRA, you typically need a background in life sciences, strong knowledge of clinical trial processes, and a relevant degree (often in nursing, pharmacy, or biology). Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and Good Clinical Practice (GCP) certification is highly valued. Attention to detail, excellent organizational skills, and strong communication abilities help build effective relationships with study sites and ensure study compliance. These competencies are crucial for maintaining regulatory standards, ensuring data integrity, and supporting the smooth execution of clinical trials.

How does a permanent in house CRA typically collaborate with clinical project teams?

A Permanent In House Clinical Research Associate (CRA) works closely with clinical project managers, site monitors, data managers, and regulatory teams to ensure the smooth conduct of clinical trials. Collaboration often involves regular meetings, detailed documentation review, and timely communication to resolve site issues or protocol deviations. Common challenges include balancing multiple studies simultaneously, managing tight deadlines, and ensuring consistent communication between remote sites and the sponsor. However, being in-house allows for easier access to cross-functional support and resources, helping to address these challenges effectively.

What is the difference between Permanent In House Cra vs Contract Cra?

AspectPermanent In House CraContract Cra
Employment TypeFull-time, ongoing employmentTemporary, project-based
Work EnvironmentIn-house, within a company's clinical research teamExternal, often at a contract research organization or site
CertificationsTypically requires similar certifications (e.g., GCP, ICH)Same certifications as permanent roles, but may vary by project
Industry UsageCommon in pharmaceutical companies and biotech firmsCommon in CROs and clinical trial sites

In summary, a Permanent In House Cra is a full-time employee working within a company's research team, offering stability and ongoing projects. A Contract Cra, on the other hand, works on temporary assignments, often through CROs, providing flexibility but less job security.

What are popular job titles related to Permanent In House Cra jobs in Oregon?

For Permanent In House Cra jobs in Oregon, the most frequently searched job titles are:

What job categories do people searching Permanent In House Cra jobs in Oregon look for?

The top searched job categories for Permanent In House Cra jobs in Oregon are:

Permanent In House Cra jobs near you

In-House Clinical Research Associate (CRA)

Praxis Precision Medicines, Inc.

OR • On-site, Remote

Full-time

Posted 18 days ago

Job description

Location: This position may be performed remotely but requires flexibility and a willingness to travel as needed. 

Position Summary 

We are seeking an In-House Clinical Research Associate (CRA) who's excited to help execute fast, high-quality clinical trials that drive our mission forward. You'll be a key player in ensuring our studies are inspection-ready, patient-centric, and run with rigor. This role supports both internal team coordination and site-facing execution-keeping timelines sharp, data clean, and communication clear. 

Primary Responsibilities 

  • Support study execution by managing meeting logistics, documenting decisions, and tracking action items.
  • Partner with Clinical Operations and site monitors to ensure protocol compliance and quality standards are met.
  • Responsible for filing the site-level documents into the Trial Master Files (TMFs)  in a timely manner
  • Track, review, and organize essential documents from sites and vendors.
  • Identify, escalate, and help resolve site-level issues in collaboration with cross-functional teams.
  • Assist with regulatory submissions and other study deliverables.
  • Drive process improvements that enhance speed, quality, and patient impact. 

Qualifications and Key Success Factors 

  • Bachelor's degree in a life science or health-related field, or equivalent industry experience.  
  • 5+ years of clinical trial experience in biotech, pharma, or CRO settings.  
  • Solid knowledge of GCP, ICH guidelines, and regulatory requirements.  
  • Exceptional organizational and communication skills.  
  • A proactive, problem-solving mindset with high attention to detail.  
  • Comfortable managing multiple priorities in a fast-paced, mission-driven environment.  
  • Strong team player who thrives in flat, agile organizations.  
  • Proficient in Microsoft Office (Word, Excel, PowerPoint, Outlook). 
  • The physical and mental requirements of our roles include but are not limited to regular use of a computer, devices or other office equipment, clear communication, and occasional movement. You'll need comfort with screen work, basic hand coordination, and focus. Reasonable accommodations may be made to enable individuals with disabilities to perform these functions. 

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