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Manager, Clinical Assessment Technologies Operations
Worldwide Clinical Trials. Oversee operational work related to rater selection, certification/qualification, training content, scale acquisition, surveillance maintenance, and workbook/source document management .
Posted 9/17/2026full-timeRemote • Alabama • United States, Canada, SamoaJuniorMid-Level💰 $90,000 - $178,000 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in managing clinical trial operations, including rater selection, training, and compliance with regulatory guidelines. Proficient in project management, data surveillance, and effective communication with stakeholders.
Highest-signal resume keywords
Clinical Trials ManagementRegulatory Compliance (SOPs, ICH/GCP)Team LeadershipData Surveillance MethodologyProject Management
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Rater SelectionTraining Content DevelopmentData ManagementDocument ManagementMicrosoft WordMicrosoft ExcelAdobePowerPointBudget ManagementPhase I-IV Clinical Research
Soft Skills
Highly OrganizedDetail-OrientedStrong Communication SkillsInterpersonal SkillsSelf-Motivation
Industry Keywords
Clinical ResearchRegulatory GuidelinesStudy-Specific TrainingInvestigators’ MeetingsCAT Operations
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Oversee operational work related to rater selection, certification/qualification, training content, scale acquisition, surveillance maintenance, and workbook/source document management
- Ensure assigned projects are timely and compliant with SOPs, ICH/GCP, and regulatory guidelines
- Coordinate completeness of rater experience qualification documents and communicate results to Sponsors and study teams
- Develop study-specific rater training web portals and ensure readiness to study timelines
- Coordinate Investigators’ Meetings and associated CAT materials
- Organize editing and formatting of didactic training presentations
- Oversee scale and study source workbook management, including licenses, translations, regulatory authorizations, and Sponsor approvals
- Maintain data surveillance methodology by tracking and reconciling source documentation and providing reports
- Provide CAT data for Final Study Reports
- Oversee archiving of CAT study documents
- Consult on rater training and data surveillance plans
- Develop and present at Sponsor Kick-Off Meetings regarding CAT operations
- Work with the Operations Director and study team to meet budgetary demands
- Manage assigned Operations staff
- Perform other duties as assigned
Requirements
What you’ll need- Highly organized, detail-oriented, and service-oriented
- Excellent planning, managing, monitoring, scheduling, and critiquing skills
- Excellent at meeting timelines consistently and effectively working under pressure
- Continuously open to constructive, developmental feedback
- Strong writing and verbal communication skills
- Strong interpersonal skills in a fast-paced, deadline-oriented, and changing environment
- Strong ability to handle multiple tasks and administrative details
- Strong self-motivation skills
- Strong ability to work in teams
- Excellent proficiency in Microsoft Word, Excel, Adobe, and PowerPoint
- Bachelor’s degree in Life Science preferred
- Two to four years of experience working in clinical trials
- At least two years of experience managing team members or leading a team; in lieu of people management experience, demonstrated ability to lead and understand policies, procedures, financial and leadership principles, time management, project management, and effective communication
- Demonstrable knowledge of Phase I-IV clinical research trials
- Ample knowledge of SOPs, ICH/GCP, and regulatory guidelines
- Competency working with data and numbers
- Fluency in English required for day-to-day business
- Willingness and ability to travel domestically and internationally
- Ability to work flexibly across different time zones when required
Benefits
Comp & perks- Competitive benefits package depending on location
- Inclusive and equitable workplace
- Transparent compensation
- Pay equity and transparency