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Worldwide Clinical Trials

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 fit
Core Competencies

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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

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Applicant Tracking System Keywords

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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 & technologies
Google 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