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Remote Clinical Trial Transparency Jobs in Oregon

Natera

Medical Director - Skin/IO

OR · On-site +1

Remote with ~40% domestic and international travel Shape the future of cancer care as a Medical ... Collaborate on clinical trial design, data analysis, and publication strategy related to ctDNA ...

eClinical Solutions

Project Manager

OR · On-site +1

Project Managers are expected to be familiar with Clinical Trial industry standards, eCS services ... for Remote Work! We have also received numerous Top Workplaces Culture Excellence Awards ...

OneStudyTeam

Senior Director, Strategic Accounts

OR · On-site +1

$140K - $190K/yr

... Clinical Development or Health-tech sectors, we want to talk with you! This is a fully remote ... Trial Leaders, CROs, and CxOs of life sciences companies that conduct clinical research. * Proven ...

Fortrea

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

OR · On-site +1

$105/hr

WHAT YOU WILL DO You will utilize your skills, knowledge, and clinical judgement to provide a high ... Varied hours may be required. #LI - Remote Applications will be accepted on an ongoing basis. Learn ...

410 ICR United States USA

CRA II

Portland, OR · Remote

$91K - $114K/yr

... clinical trial processes, regulations, and ICH-GCP guidelines. * Strong organizational and ... MM2 #LI-Remote Employment with ICON is contingent upon having the legal right to work in the ...

Icon plc

CRA II

Portland, OR · Remote

$91K - $114K/yr

... clinical trial processes, regulations, and ICH-GCP guidelines. * Strong organizational and ... MM2 #LI-Remote Employment with ICON is contingent upon having the legal right to work in the ...

Spyre Therapeutics

Senior Director, Biostatistics

OR · On-site +1

$290K/yr

... clinical trials, including contributing to trial designs, authoring statistical sections of ... Remote working environment with frequent in-person meetings to address complex problems and build ...

Care Access

Patient Recruiter

OR · On-site +1

Accurate and comprehensive documentation is crucial to ensure a smooth patient journey through the clinical trial process. * Remote Pre-Screening: * Conduct remote screening visits for specific ...

Care Access

Travel Sub-Investigator

OR · On-site +1

$46K - $47K/yr

... remote tele-medicine work to support our clinical research studies. Additionally, our Sub ... Perform trial procedures as per delegation which can include the following but not limited to:

Natera

Medical Science Liaison

OR · On-site +1

Support and coordinate clinical trial and research initiatives at academic institutions and ... This is a remote, field-based position requiring daily use of a computer and the ability to travel ...

Care Access

Senior Enterprise Performance Analyst

OR · On-site +1

$70K - $90K/yr

... accelerate clinical trial delivery * Lead both high-frequency reporting and deep-dive ad hoc ... Remote within the United States. This role requires 100% of work to be performed in a remote office ...

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All JobsClinical Trial Transparency JobsRemote Clinical Trial Transparency JobsRemote Clinical Trial Transparency Jobs in Oregon

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 Medical Director, Clinical Development

Spyre Therapeutics

OR • On-site, Remote

$343K - $365K/yr

Full-time

Medical, Retirement, PTO

Re-posted 22 days ago

Job description

Role Summary:

The Senior Director of Clinical Development for Rheumatology will contribute to the clinical development strategy and execution for innovative therapies targeting rheumatic indications. The Senior Director will play a pivotal role as a key clinical contributor within our global clinical development programs, partnering with cross-functional teams to support the design, planning, and implementation of study protocols and regulatory activities that advance the development of our cutting-edge antibody portfolio. This individual will join the Rheumatology Clinical Development team at a relatively early stage and will play a key role in directing research and formulating strategy to drive program success. 

Key Responsibilities:

  • Clinical Leadership: Contribute strategic leadership and medical expertise to the clinical development of our cutting-edge antibody portfolio in rheumatic indications.
  • Trial Management: Contribute to the study design, execution and interpretation of results, with a focus on proof-of-concept and later phases of development.  
  • Cross-functional Collaboration: Work closely with cross-functional teams including Biostatistics, Regulatory Affairs, and Clinical Operations to support integrated and strategic trial execution. 
  • Regulatory: Provide scientific/medical content and other input as appropriate for INDs, Investigator Brochures, Clinical Study reports, regulatory submissions and responses, and other program documents. Ensure compliance with regulatory standards and guidelines, including health authority requirements for MD sign-off on patient-related matters. 
  • Safety Oversight: Ensure the safety of study participants by actively participating in safety monitoring and data review processes. 
  • Stakeholder Engagement: Represent the Clinical Development function in interactions with regulatory agencies, investigators,  KOLs, and other external stakeholders, as appropriate. 
  • Other activities as required.

Ideal Candidate:

  • MD or equivalent medical degree is required. 
  • Minimum of 4+ years clinical development experience within the pharmaceutical or biotech industry within I&I indications, rheumatology strongly preferred.
  • Experience with antibody therapeutics preferred. 
  • Proven track record in designing and executing clinical trials in immunology or inflammation.
  • Experience with regulatory filings and interactions with health authorities.
  • Strong understanding of GCP, clinical trial design, statistics, and global regulatory processes. 
  • Excellent communication and interpersonal skills, with the ability to motivate teams and collaborate effectively across functions. 
  • Ability to manage complex projects in a fast-paced environment. 

What We Offer:

  • Opportunity to work in a fast-paced, dynamic environment where you help shape the culture of our young company, contribute broadly to advance meaningful medicines, and learn quickly.
  • Market competitive compensation and benefits package, including base salary, performance bonus, equity grant opportunities, health, welfare & retirement benefits.
  • Unlimited PTO
  • Two, one-week company-wide shutdowns each
  • Commitment to provide professional development opportunities.
  • Remote working environment with frequent in-person meetings to address complex problems and build relationships.

The expected salary range offer for this role is $343,000 to $365,000. Actual pay offered may vary depending on job related knowledge, experience, education, and geographic location. 

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