Clinical Scientist – FSP

Parexel

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

Posted 9/29/2026full-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 study support, including medical monitoring, imaging data reconciliation, and protocol deviation management, while effectively communicating with stakeholders and adhering to ICH-GCP standards.

Highest-signal resume keywords

Oncology ExperienceMedical MonitoringImaging Data ReconciliationAdvanced Excel SkillsClinical Development Experience

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

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

Hard Skills

Clinical Study SupportProtocol Deviation ManagementAdjudication SupportPreparation of Meeting MaterialsMS Office SuitePivot TablesVLOOKUPsOral Communication SkillsWritten Communication SkillsLife Sciences Degree

Soft Skills

Interpersonal SkillsStakeholder Interaction

Industry Keywords

ICH-GCPClinical StudiesPharmaceutical ExperienceCross-Functional LiaisonSurvival Follow-Up

About the role

Key responsibilities & impact

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

Requirements

What you’ll need

Oncology experience is required
Bachelor's, Master's, or PhD in Life Sciences with 2+ years of relevant career experience
If no degree in Life Sciences, a Bachelor's degree with significant experience in clinical development (>5 years) is required
Demonstrated oral and written communication skills
MS Office Suite experience required, including Word, Excel, and PowerPoint
Advanced Excel skills required, including pivot tables and VLOOKUPs
Proficient in written and spoken English
Experience with adjudication support, medical monitoring, imaging data reconciliation, preparation of meeting materials, and protocol deviation management
Pharmaceutical experience beneficial but not required
2 years of medical monitoring experience preferred

Benefits

Comp & perks

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