Parexel FSP is looking for Study Manager! Oncology highly preferred
Job Purpose:
The Study Manager (SM) assists the Study Management Study Lead and study team with the operational
conduct of clinical studies (e.g., clinical trial team [CTT] minutes, clinical supplies planning/tracking, lab specimen tracking, imaging data reconciliation, status update reports, study closeout activities).
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)
• May be responsible for tracking study timelines and will be proficient in
project management tools
• Liaises with cross-functional lines as appropriate
• May interact with internal and external stakeholders (study sites, vendors,
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
• 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
Education:
• Bachelors/Masters/PhD with 2+ years clinical research experience
#LI-LG4
#LI-REMOTE
