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Remote Clinical Study Start Up Jobs in Oregon (NOW HIRING)

Syneoshealth

Clinical Trial Manager - Full Service

OR · On-site +1

Clinical Trial Manager - Full Service Syneos Health is a leading fully integrated biopharmaceutical ... Collaborates with other functional leaders such as Study Start Up, Patient Recruitment and Data ...

Bausch & Lomb

Senior Manager, Clinical Trials (15543)

OR · On-site +1

... start up, enrollment, monitoring, close out and inspection readiness. Understanding of regulatory authority requirements for clinical study report submissions Experience overseeing CROs, clinical ...

Amgen

Imaging Specialist Manager

Portland, OR · On-site +1

You will manage and coordinate the operational imaging strategy, plan, risk assessment, mitigation, and execution for oncology and non-oncology clinical trials across all phases from study start-up ...

Natera

Manager, Clinical Trials

OR · On-site +1

... start-up through close-out. The Clinical Trial Manager should have experience in managing all aspects of the trials independently, and is expected to provide functional expertise to ensure that study ...

Telix Pharmaceuticals (AMER)

Global Clinical Lead

OR · On-site +1

Clinical study design and execution : Oversee the development of clinical study plans from concept ... Possess a willingness to think outside the box and come up with unique and creative solutions to ...

Stryker

Senior Staff Medical Writer (Remote)

Portland, OR · On-site +1

$143K - $238K/yr

Author clinical study protocols, study reports, data summaries, and supporting scientific documents for regulatory and clinical initiatives. * Conduct systematic literature reviews, evaluate ...

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Remote Clinical Study Start Up information

What is the difference between Remote Clinical Study Start Up vs Remote Clinical Data Coordinator?

AspectRemote Clinical Study Start UpRemote Clinical Data Coordinator
Primary ResponsibilitiesPlanning, site selection, regulatory submissions, site initiationData entry, data validation, database management, data quality assurance
Required CredentialsLife sciences degree, knowledge of GCP, regulatory knowledgeLife sciences or related degree, familiarity with clinical data systems
Work EnvironmentCollaborates with sponsors, sites, regulatory bodiesWorks mainly with data management teams and databases
Industry UsageInvolved early in trial setup phasesInvolved during data collection and analysis phases

Remote Clinical Study Start Up focuses on preparing and initiating clinical trials, including site selection and regulatory compliance. In contrast, Remote Clinical Data Coordinator manages and ensures the accuracy of clinical trial data during the study. Both roles require related credentials and work within the clinical research industry, but they operate at different stages of the trial process.

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The most popular types of Clinical Study Start Up jobs in Oregon are:

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For Remote Clinical Study Start Up jobs in Oregon, the most frequently searched job titles are:

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Remote Clinical Study Start Up jobs near you
Infographic showing various Remote Clinical Study Start Up job openings in Oregon as of August 2026, with employment types broken down into 1% As Needed, 63% Full Time, 16% Part Time, and 20% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution.

Senior Clinical Trial Manager

OR • On-site, Remote

Ultragenyx Pharmaceutical
Biotechnology Research and Development • 1 - 5K employees
Learn more about Ultragenyx Pharmaceuticalexternal

Full-time

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

Position Summary:

ultradedicated - Your biggest challenges yield rare possibilities

The Senior Clinical Trial Manager Sr. (CTM) is responsible for the day-to-day management of a clinical trial or region, oversight of vendors, and clinical trial sites. For this study, the role is as a Lead Study Manager. The Senior Clinical Trial Manager (Sr. CTM) is accountable for ensuring high quality deliverables are within timelines and budget. This position will work closely with cross-functional teams to ensure study start-up through close-out activities are conducted in accordance with Standard Operating Procedures (SOPs) and applicable regulations governing the conduct of clinical trials.

Work Model: 

Remote: Officially documented as working full-time from home, with travel to Ultragenyx's offices or other locations on occasion as needed.

Responsibilities:
  • Responsible for the day-to-day management of assigned operational aspects, such as CRO/vendor management, drug supply management, management of clinical sites, etc for assigned region(s) or study(s)
  • Manages high impact vendors, including oversight of timelines and contracts (invoicing, purchase order monitoring, and forecasting)
  • Oversee development and maintenance of study documents such as Study Timelines, Vendor Management Plan, Risk Management Plan, Informed Consent Form, Monitoring Oversight Plan, CRFs, Study Reference Manual, dashboards, etc
  • Lead, or actively contribute to, Study Management Team meetings
  • Identify study risks, develop and implement mitigation strategies
  • Oversee Trial Master File, Completeness Reviews, and Essential Document List
  • Support the study budgeting process, including the review of clinical trial financial accruals
  • Manages direct reports
  • Represents Clinical Operations on initiatives, may lead initiatives
Requirements:
  • Bachelor degree or equivalent is required (scientific or healthcare discipline preferred)
  • Typically, 8 years of direct work experience in Clinical Research, with international experience from study start up through closeout preferred
  • Fully capable to independently lead all aspects of a clinical trial
  • Effective leadership of cross-functional teams
  • Excellent planning, organizational, and communication skills
  • Able to handle multiple tasks and deadlines, and identify risks and issues and take appropriate actions
  • Must be self-motivated and able to develop solutions for a variety of complex problems where analysis requires an in-depth evaluation of variable factors, including inter-organizational impact
  • Must have the ability to build and maintain positive relationships with management, peers, vendors, and clinical sites
  • 10% travel may be required

#LI-CS1 #LI-Remote

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