Clinical Scientist – FSP

Parexel

. Assist the CS Protocol Lead and study team with the clinical/scientific conduct of clinical studies .

Posted 9/30/2026full-timeRemote • United StatesJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical study support, including medical monitoring, protocol deviation management, and stakeholder interaction. Proficient in MS Office Suite and compliance with ICH-GCPs and Parexel processes.

Highest-signal resume keywords

Medical Monitoring ExperienceClinical Study SupportMS Office Suite ProficiencyOral And Written Communication SkillsLife Sciences Degree

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Medical MonitoringProtocol Deviation ManagementClinical Study SupportData ReconciliationSurvival Follow-up Leadership

Soft Skills

Oral CommunicationWritten CommunicationStakeholder InteractionCross-Functional Liaison

Tools & Technologies

MS Office SuiteWordExcelPowerPoint

Industry Keywords

ICH-GCPClinical DevelopmentPharmaceutical ExperienceTherapeutic Area Experience

About the role

Key responsibilities & impact

Assist the CS Protocol Lead and study team with the clinical/scientific conduct of clinical studies
Support adjudication, medical monitoring, imaging data reconciliation, meeting-material preparation, and protocol deviation management
Support a single study or multiple studies
Lead a limited-scope study, such as Survival Follow-up
Liaise with cross-functional lines
Interact with internal and external stakeholders, including study sites and committees, to support clinical study objectives
Complete required training curriculum
Complete timesheets accurately
Submit expense reports
Update CV as required
Maintain knowledge of and comply with Parexel processes, ICH-GCPs, and applicable requirements

Requirements

What you’ll need

Demonstrated oral and written communication skills
MS Office Suite experience required, including Word, Excel, and PowerPoint
Proficient in written and spoken English
Proficient in local language, as applicable
Willingness to travel as required for key company meetings
Pharmaceutical experience beneficial but not required
Therapeutic Area-specific experience beneficial
2 years medical monitoring experience preferred
Bachelor's/Master's/PhD in Life Sciences with 2+ years relevant career experience
If no degree in Life Sciences, significant experience in clinical development (>5 years)

Benefits

Comp & perks

Equal opportunity employment
Willingness to travel as required for key company meetings