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Global Source Jobs in Oregon (NOW HIRING)

Care Access

Source Document Specialist

OR · Remote

$30 - $35/hr

How This Role Makes a Difference The Source Document Specialist is responsible for ensuring ... The position requires comfort working both independently and as part of a global team, managing ...

G-P

OR

$106K - $133K/yr

... source. What you'll do: * Continuous Content Lifecycle Management: Own the rolling 6-month refresh ... Stay ahead of global employment law shifts, executing rapid updates to pages when major legal ...

Rezolute

Head of Global Product Supply

Bend, OR · On-site

$245K - $257K/yr

... source of information for the Board of Directors. Principle Duties and Responsibilities Include: * Charged with designing, developing and implementing the transition of the existing, clinically ...

Telix Pharmaceuticals (AMER)

OR · On-site

$103K - $142K/yr

Define and lead Telix's global talent attraction strategy, encompassing how we source, engage, and convert exceptional talent across all markets and disciplines * Develop and activate a globally ...

Netflix

OR · On-site

$436K - $791K/yr

Together, we are writing the next episode - pushing the boundaries of storytelling, global fandom ... source control and artifact management to the CI systems that run millions of builds. We're ...

Pyramid Global Hospitality

Night Audit

Bend, OR · On-site

$17.50 - $23.25/hr

Welcome to Pyramid Global Hospitality, where people come first. As a company that values its ... While checking in, registering guests, the Front Desk Agent is a source of knowledge for the guest ...

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Global Source information

What skills and qualifications are needed to thrive as a global source?

To thrive as a Global Sourcing Specialist, you need expertise in supply chain management, procurement strategies, and international trade regulations, often supported by a degree in business or a related field. Familiarity with sourcing platforms, ERP systems like SAP or Oracle, and certifications such as CPSM or CSCP is highly valued. Strong negotiation, cross-cultural communication, and analytical thinking skills help professionals build supplier relationships and solve complex sourcing challenges. These competencies are vital for ensuring cost-effective, reliable, and compliant global supply chains.

What are common challenges faced by professionals in a global sourcing role, and how are they typically addressed?

Professionals in Global Sourcing often encounter challenges such as managing time zone differences, navigating diverse regulatory environments, and ensuring consistent quality across international suppliers. Effective communication, strong relationship-building with suppliers, and a robust understanding of international trade regulations are vital for overcoming these hurdles. Many organizations provide ongoing training and utilize collaborative digital tools to streamline processes, making it easier for sourcing teams to coordinate and respond quickly to global supply chain changes.

What is the difference between Global Source vs Procurement Specialist?

AspectGlobal SourceProcurement Specialist
CredentialsTypically requires supply chain or sourcing certifications, bachelor's degree in business or related fieldRequires procurement or supply chain certifications, bachelor's degree often in business, logistics, or related area
Work EnvironmentInternational or multinational companies, global sourcing teamsCorporate procurement departments, manufacturing or retail industries
Industry UsageUsed across industries with global supply chains, including manufacturing, retail, and technologyPrimarily in industries with complex purchasing needs like manufacturing, retail, and logistics

Global Source roles focus on managing international sourcing strategies and supplier relationships worldwide, often requiring knowledge of global markets. Procurement Specialists handle purchasing activities within specific organizations, focusing on acquiring goods and services efficiently. While both roles involve sourcing and supplier management, Global Source positions emphasize global market analysis and international negotiations, whereas Procurement Specialists concentrate on internal procurement processes and cost management.

What is a global source?

Global Source jobs typically refer to roles within companies that specialize in sourcing products, materials, or services from international suppliers. These jobs involve identifying reliable vendors worldwide, negotiating contracts, ensuring quality compliance, and managing the logistics of importing goods. Professionals in this field often work closely with manufacturers, logistics providers, and procurement teams to ensure the efficient and cost-effective acquisition of products on a global scale.
What are popular job titles related to Global Source jobs in Oregon? For Global Source jobs in Oregon, the most frequently searched job titles are:
What job categories do people searching Global Source jobs in Oregon look for? The top searched job categories for Global Source jobs in Oregon are:
What cities in Oregon are hiring for Global Source jobs? Cities in Oregon with the most Global Source job openings:
Global Source jobs near you
Infographic showing various Global Source job openings in Oregon as of August 2026, with employment types broken down into 85% Full Time, 10% Part Time, 4% Contract, and 1% Nights. Highlights an 88% Physical, 4% Hybrid, and 8% Remote job distribution.

Source Document Specialist

Care Access

OR • Remote

$30 - $35/hr

Other

Medical, Dental, Vision, Retirement, PTO

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

Job description

How This Role Makes a Difference

The Source Document Specialist is responsible for ensuring accurate, compliant, and efficient clinical trial documentation. This role translates complex study protocols into clear, structured source documents that support highquality data collection and regulatory compliance. Serving as a key partner to site staff and study teams, the Specialist manages version control, improves documentation workflows, and safeguards data integrity.

How You'll Make An Impact
  • Review and validate source documents (eSource and paper) to ensure completeness, accuracy, and alignment with study protocols, while ensuring compliance with GCP, 21 CFR Part 11, and internal SOPs.
  • Review protocol amendments and other study changes to assess impact on source documents, communicate required updates to the source team, and submit revisions as needed.    
  • Coordinating with source creators, site staff and internal teams for feedback and approval.     
  • Manage daily communication with site staff, study teams, and internal departments regarding source document updates, requests, and training support. 
  • Support quarterly initiatives, including process improvements, training development, and workflow optimizations for source documentation
  • Participate in cross-functional meetings to provide input on study start-up timelines, protocol changes, and documentation impact analysis.
  • Conduct internal audits and quality checks to ensure adherence to documentation standards and regulatory compliance
  • Provide feedback to help update standardized templates and checklists to improve the efficiency of source document review.
The Expertise Required
  • The Source Document Specialist must demonstrate a strong understanding of clinical trial protocols, GCP, and applicable regulatory requirements, including 21 CFR Part 11, to ensure compliant source documentation. Prior experience in clinical trials-particularly in a Clinical Research Coordinator (CRC) or Quality Assurance (QA) or similar role-is preferred and provides valuable insight into study workflows and data collection needs.
  • The role requires proficiency in Microsoft Excel, Word, Outlook, Teams, and SharePoint, along with the ability and willingness to work within eSource platforms such as CRIO. Strong attention to detail is essential to identify discrepancies, manage version control, and ensure accuracy and traceability of source documentation.
  • Successful candidates will demonstrate excellent organizational skills, the ability to prioritize tasks in a fastpaced environment, and effective communication skills for collaborating with site staff, study teams, and regulatory stakeholders. Strong analytical and problem-solving skills, with the ability to interpret complex study requirements are critical to success in this role. A solutionoriented mindset and the ability to assess and improve documentation workflows are equally important. The position requires comfort working both independently and as part of a global team, managing multiple systems, and adapting to evolving research and technology needs.
  • Fluency in English (reading, writing, and speaking) is required to communicate effectively with the global Source team and to review Englishlanguage protocols, manuals, and regulatory documentation.
Certifications/Licenses, Education, and Experience
  • Minimum Education:
    • Bachelor's degree in a health-related field (e.g., Life Sciences, Nursing, Public Health, or a related discipline) preferred. Equivalent work experience in clinical research may be considered.
  • Minimum Experience:
    • Minimum of 2 years of experience in clinical research, with preferred experience as a Clinical Research Coordinator (CRC) or in a role involving source documentation, study execution, or regulatory compliance.
    • Strong knowledge of clinical trial operations, including protocol interpretation, source creation, and site workflow processes.
    • Experience working with Good Clinical Practice (GCP) guidelines, 21 CFR Part 11 compliance, and clinical trial documentation standards.
    • Microsoft Excel, Word, SharePoint, and other digital documentation tools.
  • Certified Clinical Research Coordinator (CCRC) - from ACRP (Association of Clinical Research Professionals)
  • Certified Clinical Research Professional (CCRP) - from SOCRA (Society of Clinical Research Associates)
  • Good Clinical Practice (GCP) Certification - required or obtained upon hire. 
How We Work Together
  • Location: Remote within the United States. This role requires 100% of work to be performed in a remote office environment.
  • Travel: This is a remote position with less than 10% travel requirements. Occasional planned travel may be required as part of the role.
  • Physical demands associated with this position Include: The ability to use keyboards and other computer equipment.

The expected pay range for this role is $30.00 - $35.00 USD per hour for full time team members.

Benefits & Perks (US Full Time Employees)
  • Paid Time Off (PTO) and Company Paid Holidays
  • 100% Employer paid medical, dental, and vision insurance plan options
  • Health Savings Account and Flexible Spending Accounts
  • Bi-weekly HSA employer contribution
  • Company paid Short-Term Disability and Long-Term Disability
  • 401(k) Retirement Plan, with Company Match 

Mandatory Employer Disclosures:
Notice to Illinois applicants: Applicants are not obligated to disclose expunged juvenile records or adjudication, arrest, or conviction.
Notice to Connecticut applicants: Care Access may require applicants to submit to a urinalysis drug test in connection with an application for employment.
Notice to Arizona, Georgia, Indiana, and North Dakota applicants: Care Access complies with applicable laws prohibiting smoking in and around places of employment.
Notice to Massachusetts applicants: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Notice to Rhode Island applicants: Care Access complies with Rhode Island law prohibiting smoking in enclosed areas within places of employment. Care Access is also subject to is subject to Chapters 29-38 of Title 28 of the Rhode Island General Laws.
Notice to Maryland applicants: UNDER MARYLAND LAW, AN EMPLOYER MAY NOT REQUIRE OR DEMAND, AS A CONDITION OF EMPLOYMENT, PROSPECTIVE EMPLOYMENT, OR CONTINUED EMPLOYMENT, THAT AN INDIVIDUAL SUBMIT TO OR TAKE A LIE DETECTOR OR SIMILAR TEST. AN EMPLOYER WHO VIOLATES THIS LAW IS GUILTY OF A MISDEMEANOR AND SUBJECT TO A FINE NOT EXCEEDING $100. 

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