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Remote Clinical Trial Transparency Jobs in Oregon

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Clinical Research Associate II

Portland, OR · Remote

Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...

Natera

Senior Accountant

OR · On-site +1

$73K - $92K/yr

This individual will also support process improvements and technical accounting reviews related to clinical trial agreements and research activities. This is a fully remote position, offering the ...

Natera

Senior Program Manager

OR · On-site +1

$115K - $116K/yr

Remote or On-Site in Boulder, CO (Foresight Dx business unit, a Natera company) Foresight ... Programs may span new product development, mature products, research programs, and 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

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Remote Clinical Trial Transparency information

What is a remote clinical trial transparency professional?

A Remote Clinical Trial Transparency professional is responsible for ensuring that information about clinical trials is accurately disclosed and made accessible to the public, regulators, and other stakeholders while working remotely. Their work involves preparing, reviewing, and submitting clinical trial data, maintaining compliance with global regulations, and protecting patient confidentiality. They ensure transparency by posting trial results to public registries, responding to disclosure requests, and supporting ethical standards in clinical research.

What are the key skills and qualifications needed to thrive as a remote clinical trial transparency specialist?

To thrive as a Remote Clinical Trial Transparency Specialist, you need a solid understanding of clinical research processes, regulatory requirements (like FDA, EMA, or ICMJE), and often a degree in life sciences or healthcare. Familiarity with trial disclosure platforms (such as ClinicalTrials.gov and EudraCT), document management systems, and data anonymization tools is typically required. Strong attention to detail, analytical thinking, and effective written communication are crucial soft skills for ensuring accuracy and compliance. These abilities are vital to uphold regulatory standards, protect patient privacy, and promote trust through transparent clinical trial reporting.

What are some common challenges faced by professionals in a remote clinical trial transparency role, and how can they be addressed?

Professionals in Remote Clinical Trial Transparency roles often encounter challenges such as managing large volumes of sensitive data, ensuring regulatory compliance across multiple jurisdictions, and coordinating with global stakeholders virtually. Effective organization, strong communication skills, and staying up to date with evolving regulations are key to addressing these challenges. Utilizing secure data management platforms and fostering clear communication channels with cross-functional teams can help ensure both transparency and compliance in a remote environment.

What is the difference between Remote Clinical Trial Transparency vs Remote Clinical Data Manager?

AspectRemote Clinical Trial TransparencyRemote Clinical Data Manager
Primary FocusEnsuring transparency of clinical trial results and compliance with reporting regulationsManaging and cleaning clinical trial data for analysis and reporting
Required CredentialsRegulatory knowledge, clinical trial experience, often a degree in life sciencesBiostatistics, data management certifications, degree in health sciences or related field
Work EnvironmentRemote, regulatory agencies, pharmaceutical companies, CROsRemote, pharmaceutical companies, CROs, data management teams

While both roles operate remotely within the clinical research industry, Remote Clinical Trial Transparency focuses on reporting compliance and transparency of trial results, whereas Remote Clinical Data Managers handle the technical aspects of data collection and management. Both require knowledge of clinical processes but serve different functions in the clinical trial lifecycle.

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

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

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

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

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

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

Remote Clinical Trial Transparency jobs near you

Senior Clinical Trial Manager

Ultragenyx Pharmaceutical

OR • On-site, Remote

Full-time

Posted 4 days ago

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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