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The Clinical Scientist (CS) assists the CS Protocol Lead and study team with the clinical/scientific conduct of clinical studies.
Job Responsibility:
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)
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
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, ICH-GCPs and other applicable requirements
Requirements:
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)
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
Pharmaceutical experience beneficial but not required
Therapeutic Area (TA) specific experience beneficial
2 years medical monitoring experience preferred
Nice to have:
Pharmaceutical experience beneficial
Therapeutic Area (TA) specific experience beneficial