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Thermo Fisher Scientific

Safety Committee Administrator

Thermo Fisher Scientific

. Coordinate DSMB/EAC projects and provide safety support on global and domestic programs .

Posted 10/14/2026full-timeRemote • North Carolina • United StatesJuniorMid-LevelWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates strong project coordination capabilities, including managing DSMB/EAC projects, facilitating meetings, and ensuring compliance with FDA regulations and ICH Good Clinical Practices. Proficient in data analysis, communication, and maintaining audit readiness while effectively managing multiple tasks under strict deadlines.

Highest-signal resume keywords
Project CoordinationData AnalysisFDA Regulations KnowledgeEffective CommunicationAttention to Detail

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Project ManagementData EntryMeeting FacilitationContract AdministrationDocument PreparationAudit ReadinessReconciliationConfidentiality AgreementsTraining ManagementLogistics Coordination
Soft Skills
Problem-SolvingRelationship BuildingIndependenceFlexibilityInterpersonal Skills
Tools & Technologies
MS OfficeExcelWordPowerPointAccess
Certifications & Qualifications
High School DiplomaVocational Qualification
Industry Keywords
Good Clinical PracticesFDA RegulationsSOPsData PrivacyProject TeamsClient LiaisonCommittee ManagementTeleconference CoordinationInvestigative SitesMember Agreements

About the role

Key responsibilities & impact
  • Coordinate DSMB/EAC projects and provide safety support on global and domestic programs
  • Set up DSMBs/EACs, execute and track member contracts, and administer member payments and honoraria
  • Poll committee members and client contacts to schedule meetings
  • Arrange meeting facilities and attend meetings, completing meeting minutes
  • Represent the DSMB/EAC Coordination Team at global and domestic meetings via teleconference and face-to-face formats
  • Coordinate logistics and assist with meeting facilitation alongside clients, board members, vendors and project teams
  • Prepare and coordinate approval of Confidentiality Disclosure Agreements, Letters of Intent and Member Agreements
  • Compile, create and submit follow-up to investigative sites
  • Coordinate project meetings, draft minutes, and distribute blinded/unblinded materials through client portals
  • Manage project training and program file setup, maintenance and archival
  • Maintain PV audit readiness
  • Identify and redact subject identifiers, retrain sites and escalate recurring issues to Data Privacy
  • Enter data into databases and tracking systems and perform reconciliations
  • Oversee committee, travel and translation expenses and escalate issues for timely member payment
  • Support specialty committee team activities
  • Obtain and track adjudication documents and assist with dossier building and distribution
  • Liaise with internal functional teams to implement projects and manage contracted services

Requirements

What you’ll need
  • High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification
  • Technical positions may require a certificate
  • At least 2 years of previous relevant experience (or equivalent combination of education, training and/or directly related experience)
  • Strong problem-solving skills
  • Ability to work independently with minimal supervision and demonstrate initiative
  • Ability to build strong relationships
  • Ability to analyze project-specific data/systems for accuracy and efficiency
  • Ability to liaise and communicate respectfully and diplomatically with clients, management, project teams and internal staff
  • Effective oral and written communication and interpersonal skills
  • Excellent computer skills, including MS Office (Word, Excel, PowerPoint, Access)
  • Ability to prioritize and perform multiple tasks under strict deadlines
  • Strong attention to detail and accuracy
  • Flexibility to reprioritize workload according to changing project timelines
  • Working knowledge of applicable FDA Regulations, ICH Good Clinical Practices, company/client SOPs and WPDs
  • Occasional travel may be required
  • Occasional drives to site locations

Benefits

Comp & perks
  • Health and wellbeing support
  • Healthy and balanced work environment
  • Collaboration and professional development opportunities
  • Global team environment
  • Potential travel opportunities