Clinical Trial Associate

Perspective Therapeutics

. Provide comprehensive administrative and operational support to the Clinical Operations Team .

Posted 11/3/2026full-timeRemote • United StatesJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in clinical operations support, including compliance with GCP guidelines and effective management of clinical study documentation. Proficient in coordinating meetings, data collection, and communication with stakeholders in a team-oriented environment.

Highest-signal resume keywords

Clinical Operations SupportGCP Guidelines FamiliarityMicrosoft Office ProficiencyOrganizational SkillsClear Communication Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Study Documentation ManagementETMF TrackingCompliance ChecksData Collection OrganizationMeeting Coordination

Soft Skills

Attention to DetailTeam CollaborationVerbal CommunicationWritten Communication

Tools & Technologies

EQMS SystemElectronic Trial Master File

Industry Keywords

ICH-GCPFDA RegulationsClinical TrialsLife SciencesHealthcare

About the role

Key responsibilities & impact

Provide comprehensive administrative and operational support to the Clinical Operations Team
Provide general administrative support to Clinical Operations and Project Management Departments
Assist Clinical Operations teams with ongoing study conduct and required project tasks
Coordinate internal and external meetings, prepare activities, and generate meeting minutes
Facilitate outreach to potential clinical trial sites and initial site feasibility procedures
Lead quarterly documentation and compliance checks using internal trackers and the eQMS system
Act as super user for the electronic Trial Master File system and track eTMF progress
Create professional slide presentations for internal and external stakeholders
Set up, collect, register, organize, and maintain clinical study documentation
Prepare documentation for audits, final reconciliation, and archival according to GCP guidelines
Coordinate ordering, dispatch, and tracking of study materials
Organize data collection forms and other study materials, including logging, tracking, and quality control
Assist with tracking and distribution of correspondence and reports
Coordinate document translation

Requirements

What you’ll need

Bachelor's degree in a relevant field (life sciences, healthcare, etc.)
Research or health care-related academic or work experience preferred
Excellent computer literacy and application skills, including Microsoft Word, Excel, PowerPoint, and Outlook
Ability to become familiar with ICH-GCP, FDA, and other appropriate regulations and relevant SOPs
Strong organizational skills and ability to manage multiple tasks with meticulous attention to detail
Ability to work collaboratively in a team-oriented environment
Clear written and verbal communication skills in English
May be required to sit or stand for long periods of 8+ hours a day