REDCap Cloud Study Specialist

Job Title:

REDCap Cloud Study Specialist Job Description The REDCap Cloud Study Specialist designs, builds, and validates clinical study databases and electronic data capture solutions that support a high-profile NIH clinical research program. This role translates clinical trial protocols into robust technical configurations within REDCap Cloud and other EDC platforms, ensuring data integrity, regulatory compliance, and smooth system integrations. The specialist collaborates closely with Agile teams and end users to configure studies, perform user acceptance testing, and provide technical support for clinical research operations. Responsibilities Design and build clinical studies and databases in the REDCap Cloud platform, including electronic Case Report Forms (eCRFs), surveys, and related clinical data structures. Configure and manage electronic data capture (EDC) solutions, including ePRO and other clinical data collection tools, based on study protocols and requirements. Program complex validation rules, edit checks, and data queries to ensure data quality, consistency, and regulatory compliance. Translate clinical trial protocols and study requirements into detailed technical system specifications and configurations. Perform user acceptance testing (UAT) for study builds and system changes, documenting results and addressing issues identified during testing. Execute validation activities and maintain thorough documentation to support compliance with 21 CFR Part 11, Good Clinical Practice (GCP), and internal quality standards. Assist users and customers with configuration and usage questions related to REDCap Cloud and other EDC platforms, providing timely technical support and guidance. Collaborate with Agile development teams to support the design, development, and implementation of clinical data management solutions. Assist with data exports, reporting, and integration with statistical tools such as SAS, R, and SPSS to support analysis and reporting needs. Support integrations with external systems as needed, ensuring data flows are accurate, secure, and aligned with study requirements. Document system configurations, changes, workflows, and validation activities in a clear and compliant manner. Contribute to continuous improvement of study build processes, configuration standards, and documentation practices. Essential Skills Bachelor's degree in life sciences, computer science, or a related field. At least 3 years of study build experience with an Electronic Data Capture (EDC) platform such as REDCap, Medidata Rave, Veeva, or similar systems. Hands-on experience designing and configuring eCRFs, surveys, and clinical databases in an EDC environment. Proficiency with REDCap Cloud or comparable EDC platforms, including study setup, configuration, and maintenance. Demonstrated ability to program complex validation rules, edit checks, and data queries to support high-quality clinical data. Experience working with systems compliant with 21 CFR Part 11 and Good Clinical Practice (GCP). Proven experience performing user acceptance testing (UAT) for clinical systems or study builds, including test planning and execution. Strong skills in translating clinical trial protocols into detailed technical system requirements and configurations. Ability to assist with data exports, reporting, and integration with statistical tools such as SAS, R, or SPSS. Solid understanding of clinical data management processes and workflows in a regulated environment. Strong problem-solving skills and attention to detail in a technical and compliance-focused setting. Effective communication skills to collaborate with Agile teams, stakeholders, and end users. Additional Skills & Qualifications Experience as a REDCap Cloud Study Builder or Systems Integration Specialist. Background in configuring and validating electronic patient-reported outcomes (ePRO) solutions. Familiarity with surveys and patient-facing data collection tools in clinical research. Experience supporting integrations between EDC platforms and external systems or tools. Exposure to large-scale or high-profile clinical research programs. Interest in working on initiatives aligned with national clinical research priorities. Ability to work effectively in Agile development environments and cross-functional teams. Work Environment This role operates in a hybrid work model, combining on-site and remote work to support flexibility and collaboration. The position typically requires three days per week on site and two days working from home, with remote days used at the employee's discretion in coordination with team needs. The on-site location offers free parking and is situated in Bethesda. The work environment centers on configuring and supporting REDCap Cloud and other EDC platforms, collaborating with Agile teams, and engaging with clinical research stakeholders involved in a well-funded, high-profile NIH program. The role involves regular use of clinical data management systems, statistical tools such as SAS, R, and SPSS, and other technical platforms that support clinical trial operations and integrations. Job Type & Location This is a Contract position based out of Rockville, MD. Pay and Benefits The pay range for this position is $40.00 - $50.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a hybrid position in Rockville,MD.

Application Deadline This position is anticipated to close on Jun 22, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

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Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

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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. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.