Clinical Scientist- FSP
Parexel · United States
FULL-TIME
Posted Nov 12, 2026
Job Description
PXL is hiring a Clinical Scientist!
Job Purpose
The Clinical Scientist (CS) assists the CS Protocol Lead and study team with the clinical/scientific conduct of clinical studies (e.g., adjudication support, medical monitoring, imaging data reconciliation preparation of meeting materials, protocol deviation management).
Key Accountabilities
May include but not limited to the following:
Clinical Trial Operational Delivery
May support a single study or multiple studies
May lead a study with limited scope (e.g., Survival Follow-up)
Liaises with cross-functional lines as appropriate
May interact with internal and external stakeholders (study sites,
committees, etc.) in support of clinical study objectives
Compliance with Parexel Standards
Complies with required training curriculum
Completes timesheets accurately as required
Submits expense reports as required
Updates CV as required
Maintains a working knowledge of and complies with Parexel processes,
Skills
ICH-GCPs and other applicable requirements
Demonstrated oral and written communication skills
MS Office Suite Experience Required– including Word, Excel, and Power Point
Proficient in written and spoken English
Proficient in local language (as applicable)
Willingness to travel as required for key company meetings
Knowledge And Experience
Pharmaceutical experience beneficial but not required
Therapeutic Area (TA) specific experience beneficial
2 years medical monitoring experience preferred
Education
Bachelors/Masters/PhD in Life Sciences with 2+ years relevant career experience
If no degree in Life Sciences, must have significant experience in clinical development (>5 years)
Job Purpose
The Clinical Scientist (CS) assists the CS Protocol Lead and study team with the clinical/scientific conduct of clinical studies (e.g., adjudication support, medical monitoring, imaging data reconciliation preparation of meeting materials, protocol deviation management).
Key Accountabilities
May include but not limited to the following:
Clinical Trial Operational Delivery
May support a single study or multiple studies
May lead a study with limited scope (e.g., Survival Follow-up)
Liaises with cross-functional lines as appropriate
May interact with internal and external stakeholders (study sites,
committees, etc.) in support of clinical study objectives
Compliance with Parexel Standards
Complies with required training curriculum
Completes timesheets accurately as required
Submits expense reports as required
Updates CV as required
Maintains a working knowledge of and complies with Parexel processes,
Skills
ICH-GCPs and other applicable requirements
Demonstrated oral and written communication skills
MS Office Suite Experience Required– including Word, Excel, and Power Point
Proficient in written and spoken English
Proficient in local language (as applicable)
Willingness to travel as required for key company meetings
Knowledge And Experience
Pharmaceutical experience beneficial but not required
Therapeutic Area (TA) specific experience beneficial
2 years medical monitoring experience preferred
Education
Bachelors/Masters/PhD in Life Sciences with 2+ years relevant career experience
If no degree in Life Sciences, must have significant experience in clinical development (>5 years)
Additional Details
- City
- United States
- Country
- US
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