Study Manager

Thermo Fisher Scientific

Study Manager supporting the delivery of clinical studies in a global team environment. Responsible for oversight, vendor management, and ensuring compliance with study protocols and regulations.

Posted 5/6/2026full-timeRemote • 🇧🇬 BulgariaMid-LevelSeniorWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Contributing to delivering the clinical study to time, cost and quality
Ensuring inspection readiness by overseeing study eTMF completeness
Working in partnership with Study Delivery Lead on operational study delivery activities
Monitoring study conduct and progress, identifying and resolving risks/issues
Reviewing key clinical documents and leading development of study plans
Facilitating interactions and meetings with internal and external partners
Responsible for vendor management and CRO oversight

Requirements

What you’ll need

University degree or equivalent, preferably in medical or biological science
At least 3+ years of relevant work experience in a pharmaceutical/scientific environment
Knowledge of clinical trials, drug development process
Excellent knowledge of ICH-GCP, clinical study delivery process
Familiar with key systems used in clinical trial delivery
Strong project management skills and good leadership skills
Excellent verbal and written communication in English
Experience using Trial Master File industry accepted standard

Benefits

Comp & perks

Health insurance
401(k) matching
Flexible work arrangements
Professional development opportunities
Wellness programs

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

clinical trialsdrug development processICH-GCPproject managementvendor managementCRO oversightstudy plans developmenteTMF completenessrisk identificationissue resolution

Soft Skills

leadershipcommunicationcollaborationproblem-solvingorganizational skillsinterpersonal skillsfacilitationmonitoringtime managementadaptability