About this role
About this Role
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, ICH-GCPs and other applicable requirements
Skills
- Demonstrated oral and written communication skills
- MS Office Suite Experience Required– including Word, Excel, and Power Point
- Advanced Excel skills required (pivot tables, v-lookups)
- Proficient in written and spoken English
- Willingness to travel as required for key company meetings
Knowledge and Experience:
- Pharmaceutical experience beneficial but not required
- Oncology experience is required
- 2 years medical monitoring experience preferred
- Experience with adjudication support, medical monitoring, imaging data reconciliation preparation of meeting materials, and protocol deviation management
Education
- Bachelors/Masters/PhD in Life Sciences with 2+ years relevant career experience
- If no degree in Life Sciences, must have Bachelor's degree with significant experience in clinical development (>5 years)