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Remote Clinical Trial Operations Jobs in Oregon (NOW HIRING)

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Clinical Research Associate II

Portland, OR · Remote

... smooth trial operations. Your Profile: You will have a strong foundation in clinical trial ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...

Syneoshealth

Clinical Trial Manager - Full Service

OR · On-site +1

Uses prior clinical experience, operational data, metrics and reports to identify risks to clinical trial management deliverables. Escalates to the project manager any risks to clinical trial ...

OneStudyTeam

Senior Data Scientist

OR · On-site +1

$140K - $190K/yr

... clinical trial operations and a passion for improving patient outcomes through data. The expected pay range for this role is $140,000 - $190,000 USD per year for full time team members. #LI-Remote

Praxis Precision Medicines, Inc.

TMF Operations Lead

OR · On-site +1

$33.50 - $45.75/hr

As our Trial Master File expert, you'll partner with Clinical Operations and cross-functional teams to build high-quality TMFs, identify and address risks early, and help ensure our studies are ...

Avalyn Pharma

Director, Clinical Development

OR · On-site +1

Serve as the medical leader for the clinical trial team, partnering closely with Clinical Operations, Biostatistics, Regulatory Affairs, Pharmacovigilance, Translational Science, and external CROs.

Natera

Senior Accountant

OR · On-site +1

$73K - $92K/yr

... clinical trial agreements and research activities. This is a fully remote position, offering the ... Partner cross-functionally with Clinical Operations, Legal, Procurement, and FP&A to ensure ...

Natera

Senior Manager, Clinical Trials

OR · On-site +1

This Senior Manager, Clinical Trial is responsible for managing all aspects of clinical trials to ... This role manages clinical operations staff and all aspects of the trials independently, including ...

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Remote Clinical Trial Operations information

What is the difference between Remote Clinical Trial Operations vs Remote Clinical Trial Coordinators?

AspectRemote Clinical Trial OperationsRemote Clinical Trial Coordinators
ResponsibilitiesOversees trial processes, manages site logistics, ensures complianceSupports trial activities, manages participant schedules, assists with data collection
Required CredentialsTypically requires a degree in life sciences, clinical research certificationOften requires a degree or certification in clinical research or related field
Work EnvironmentRemote, with collaboration across sites and teamsPrimarily remote, working closely with trial sites and participants
Industry UsageCommon in pharmaceutical and biotech companiesCommon in research organizations and CROs

Remote Clinical Trial Operations professionals focus on managing and overseeing the entire trial process, ensuring compliance and efficiency. In contrast, Remote Clinical Trial Coordinators handle day-to-day participant management and data collection. Both roles require clinical research knowledge and often work remotely, but their scope and responsibilities differ significantly.

What are the most commonly searched types of Clinical Trial Operations jobs in Oregon?

The most popular types of Clinical Trial Operations jobs in Oregon are:

What are popular job titles related to Remote Clinical Trial Operations jobs in Oregon?

For Remote Clinical Trial Operations jobs in Oregon, the most frequently searched job titles are:

What job categories do people searching Remote Clinical Trial Operations jobs in Oregon look for?

The top searched job categories for Remote Clinical Trial Operations jobs in Oregon are:

What cities in Oregon are hiring for Remote Clinical Trial Operations jobs?

Cities in Oregon with the most Remote Clinical Trial Operations job openings:

Remote Clinical Trial Operations jobs near you

Senior Clinical Trial Manager (CTM)

Praxis Precision Medicines, Inc.

OR • On-site, Remote

Full-time

Re-posted 28 days ago

Job description

Senior Clinical Trial Manager (CTM) 

Location:   This position may be performed remotely with travel to the Boston area as needed.   

Position Summary 

This role will be responsible for project management in the initiation, execution and close out of domestic and international clinical studies, including study concept and design, feasibility assessments, study start-up, contract and budget oversight, data exchange and support of data analysis and interpretation. 

This position requires both the knowledge and experience to work within established clinical trial paradigms while exploring and embracing new approaches to conducting research to support data aggregation and analysis to advance patient care. The Sr. CTM will participate on clinical project teams to achieve quality results in a cost-effective and timely manner. S/he will be a key team member to establish key practices and procedures for the clinical team. 

Primary Responsibilities 

  • Manage study activities in the successful execution of clinical trials from protocol concept to clinical study report, complying with Good Clinical Practice (GCP) guidelines and international regulations 
  • Manage strategic engagement with key collaborators 
  • Set-up and oversee clinical trial-related trackers such as regulatory documents, trial master file (TMF), startup progress, screening/enrollment, study invoices/payments, project budgets, etc. 
  • Key contributor to IRB/EC and regulatory submissions 
  • Oversee TMF reviews to ensure completeness and inspection readiness 
  • Regularly review documents to ensure adherence to Clinical Operations and/or project specific quality requirements (e.g. SOPs, work practices, training guides) 
  • Identify and mitigate against study risks, escalating as necessary 
  • Direct initiatives to identify and implement best practices and continuous improvement plans in clinical development 

Education and Professional Experience 

  • Bachelor's degree in a scientific field required; advanced scientific degree a plus 
  • 5+ years directly managing clinical trials in Sponsor or CRO setting 
  • In-depth knowledge of clinical trial operations, ICH, GCP Guidelines and other applicable regulatory requirements 
  • Experience directing members of clinical operations teams 
  • Experience working in a team across multiple functional areas (e.g., Quality Assurance, Data Management, Biostats, Medical Writing, Safety, Clinical Supply, Finance) 

Other Essentials and Key Success Factors 

  • Intellectual curiosity, innovation and creative problem solving with an entrepreneurial spirit 
  • Ability to think critically in fast-paced projects with a keen sense of urgency and demonstrated ability to problem solve 
  • Self-motivated and able to work autonomously, as well as a member of a collaborative team 
  • Highly-organized and detail-oriented with a passion to deliver quality results 
  • Strong verbal and written communication skills with an ability to build relationships internally and externally 
  • Highest levels of professionalism, confidence, personal values and ethical standards 

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