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Remote Clinical Data Manager Contract Jobs in Oregon

As an AI Learning Project Manager, you will be tasked with driving strategic initiatives that ... Collect, analyze, and interpret data to identify trends, measure the impact of initiatives, and ...

Project Manager

OR ยท On-site +1

Clinical Trial Industry, EDC/Database implementation, Data Management, and/or Biostatistical and ... for Remote Work! We have also received numerous Top Workplaces Culture Excellence Awards ...

Global Clinical Lead

OR ยท On-site +1

... managing complex clinical development programs from concept through execution * Strategic and scientific acumen : Strong knowledge of clinical trial design, data interpretation, and the ability to ...

The Director, Clinical Development works cross-functionally with Clinical Operations, Biostatistics, Regulatory Affairs, Pharmacovigilance, Translational Science, Data Management, and external CROs ...

Contract Specialist

OR ยท On-site +1

Nice to Have Experience with vendor management processes including RFP coordination, vendor risk assessment, and renewal management. Familiarity with AI-related contract provisions, including data ...

Showing results 21-40

Remote Clinical Data Manager Contract information

What is a remote clinical data manager contract?

A Remote Clinical Data Manager Contract is a temporary, project-based position where a professional oversees the collection, validation, and management of clinical trial data from a remote location. Clinical Data Managers ensure the accuracy, integrity, and compliance of data used in clinical research, collaborating with study teams and using specialized software. Working remotely allows for flexibility and may involve coordinating across different time zones, but the core responsibilities remain the same as onsite roles. Contract positions typically last for the duration of a specific trial or project.

What are the key skills and qualifications needed to thrive as a remote clinical data manager on a contract basis?

To thrive as a Remote Clinical Data Manager on contract, you need expertise in clinical data management, database design, and a background in life sciences or related fields, often supported by a relevant degree. Familiarity with data management systems like Medidata Rave, Oracle Clinical, and knowledge of CDISC standards or certifications such as CCDM are highly valued. Strong attention to detail, excellent organizational skills, and effective remote communication are crucial soft skills for success in this role. These competencies ensure the accuracy, integrity, and security of clinical trial data, which is vital for regulatory compliance and successful study outcomes.

What are some common challenges faced by remote clinical data managers working on a contract basis, and how can they be managed?

Remote Clinical Data Managers on contract often encounter challenges such as coordinating efficiently with cross-functional teams in different locations and time zones, maintaining data integrity across multiple platforms, and adapting quickly to new study protocols or sponsor requirements. Effective communication tools, regular virtual meetings, and well-organized documentation can help bridge gaps and ensure smooth collaboration. Staying proactive in seeking clarifications and leveraging project management software are also key strategies for managing remote workflow and meeting tight study timelines.

What is the difference between Remote Clinical Data Manager Contract vs Remote Clinical Data Coordinator?

AspectRemote Clinical Data Manager ContractRemote Clinical Data Coordinator
CredentialsBachelor's in Life Sciences, Biostatistics, or related field; experience with data management systemsSimilar credentials; often entry to mid-level experience in data entry and management
Work EnvironmentContract-based, remote, project-specificRemote, often full-time or part-time, supporting clinical trial data collection
Employer & Industry UsagePharmaceuticals, biotech, CROsPharmaceuticals, clinical research organizations, healthcare companies

The Remote Clinical Data Manager Contract focuses on managing and analyzing clinical trial data on a contractual basis, requiring advanced data management skills. The Remote Clinical Data Coordinator handles data entry and coordination tasks, often supporting data collection processes. Both roles are remote and industry-specific, but differ in scope and level of responsibility.

What are popular job titles related to Remote Clinical Data Manager Contract jobs in Oregon?

For Remote Clinical Data Manager Contract jobs in Oregon, the most frequently searched job titles are:

What job categories do people searching Remote Clinical Data Manager Contract jobs in Oregon look for?

The top searched job categories for Remote Clinical Data Manager Contract jobs in Oregon are:

What cities in Oregon are hiring for Remote Clinical Data Manager Contract jobs?

Cities in Oregon with the most Remote Clinical Data Manager Contract job openings:

Infographic showing various Remote Clinical Data Manager Contract job openings in Oregon as of August 2026, with employment types broken down into 73% Full Time, 9% Temporary, and 18% Contract. Highlights an 100% Remote job distribution.

Lead Data Manager/SAS programmer (Job 1425)

DLH

OR โ€ข On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 15 days ago


Job description

About Us

DLH delivers improved health and national security readiness solutions for federal programs through science research and development, systems engineering and integration, and digital transformation. Our experts in public health, performance evaluation, and health operations solve the complex problems faced by civilian and military customers alike by leveraging advanced tools - including digital transformation, artificial intelligence, data analytics, cloud enablement, modeling, and simulation, and more. DLH is dedicated to the idea that "Your Mission is Our Passion" and brings a unique combination of government sector experience, proven methodology, and unwavering commitment to innovation to improve the lives of millions.

Overview

We are currently seeking a Lead Data Manager/SAS Programmer who will provide senior-level leadership, technical direction, and data management and statistical programming expertise for federally funded and commercially funded clinical research and epidemiological studies. You will be a senior member of a multidisciplinary team that includes data managers and programmers, epidemiologists, statisticians, and operations staff. You will play a critical role in establishing technical approaches and standards for the collection, management, integration, and delivery of research data across the full lifecycle of complex studies.

This position will lead the design and implementation of complex data management systems, data processing programs, and automated workflows that support clinical research and public health programs. You will provide technical oversight for study data management and programming activities, identify opportunities to improve efficiency and standardization, and guide the development of scalable solutions that support data quality, integrity, and reproducibility. This position will also serve as a senior technical resource and mentor for data management and programming staff, providing guidance on complex technical challenges and promoting consistent, high-quality practices across projects. This position offers significant opportunities for professional development, innovation, and collaboration across disciplines.

Responsibilities

  • Provide senior technical leadership and oversight for data management and programming activities across clinical, observational, and epidemiologic research studies, from study start-up through database closeout.
  • Lead the development of technical approaches and study data strategies, including database architecture, data workflows, data specifications, collection instruments, validation rules, data integration processes, and data delivery requirements.
  • Design, develop, and oversee complex SAS programming solutions for cleaning, transforming, validating, integrating, and managing research data, including reusable and automated programming frameworks.
  • Establish and oversee data quality and validation processes, including programmed data checks, data reconciliation, discrepancy resolution, QC procedures, and review of complex datasets, programs, and technical deliverables.
  • Provide technical direction for the integration and reconciliation of data from multiple sources, ensuring data integrity, consistency, completeness, traceability, and appropriate documentation of data transformations and decisions.
  • Oversee the development and delivery of study datasets, reports, extracts, interim data cuts, and final data deliverables, ensuring that technical solutions meet study requirements and organizational standards.
  • Develop and promote standardized, scalable, and efficient data management and programming practices, including automation, reusable programming solutions, version control, documentation standards, and continuous process improvement.
  • Provide technical mentorship and oversight to data management and programming staff, including reviewing technical approaches, guiding resolution of complex data issues, supporting work planning and prioritization, and promoting consistent programming and QC practices.
  • Serve as a senior technical advisor and collaborator to investigators, statisticians, epidemiologists, and operations staff, translating scientific and operational requirements into effective data management and programming solutions.
  • Contribute to organizational standards, processes, and best practices for research data management and programming, and ensure activities comply with study requirements, organizational SOPs, applicable regulatory and privacy requirements, and established data standards.

Qualifications

  • B.S. degree in computer science, health sciences, statistics, data science, or another related field, with ten or more years of progressively responsible experience in programming and data management for health research. -OR-
  • M.S. degree in computer science, health sciences, statistics, data science, or another related field, with eight or more years of progressively responsible experience in programming and data management for health research.
  • Advanced SAS programming capabilities, including extensive experience with DATA and PROC steps, macro programming, data transformation and integration, complex data validation, and development of efficient, reusable, and automated programming solutions.
  • Extensive experience managing complex research data, preferably within clinical, observational, epidemiologic, or other biomedical research studies, with demonstrated experience leading data management activities for complex studies.
  • Expert understanding of the full research data lifecycle, including study start-up, database architecture and development, data collection, data cleaning, reconciliation, quality control, data delivery, and database closeout.
  • Demonstrated ability to provide technical direction and oversight for complex data management and programming activities, including defining technical approaches, evaluating solutions, identifying risks, establishing priorities, and ensuring high-quality deliverables.
  • Extensive experience integrating and reconciling data from multiple sources, with the ability to resolve complex data issues and establish approaches that maintain data integrity, traceability, scalability, and reproducibility.
  • Demonstrated experience developing and implementing data quality and QC frameworks, including establishing standards, reviewing technical approaches and deliverables, and identifying opportunities to improve data quality and operational efficiency.
  • Excellent leadership, communication, collaboration, and mentoring skills, with the ability to provide technical guidance to data management and programming staff and effectively communicate complex technical concepts to multidisciplinary teams and senior stakeholders.
  • Familiarity with clinical research data standards and regulations, such as NIH Common Data Elements, CDISC, OMOP, HIPAA, 21 CFR Part 11, GCP, and FAIR principles.
  • Experience with two or more of the following is highly desirable: R, Python, SQL, database architecture and development, Git or other version control systems, APIs, and other tools used to develop efficient, scalable, and automated research data workflows.

Basic Compensation: $130,000 - $175,000 yearly salary

The salary range listed reflects what we reasonably expect to pay for this role at the time of posting. The final offer may vary based on skills, experience, geographic location, market conditions, and internal equity. Additional compensation may include performance incentives and program-specific awards. We do not use salary history to determine compensation, in line with applicable law.

Benefits

DLH Corp offers our employees an excellent benefits package, including Personal Time Off (PTO), medical, dental, vision, supplemental life with AD&D, short and long-term disability, flexible spending accounts, parental leave, legal services, and more. We want our employees to save for their future; therefore, we offer a 401(k) Retirement Plan, which includes a matching component. DLH is dedicated to your career development, providing training to help drive success, with access to our best-in-class e-learning suite for formal and informal learning, professional and technical certification preparation, and education assistance at accredited institutions.

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