Job description
PXL FSP has an exciting opportunity for a Study Manager (SM)!
Position 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).
Organizational Relationships:
- Reports to Parexel (PXL) assigned Line Manager with day-to-day direction from the Client
- 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
Primary Duties:
- 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
- Complete training assigned by Client and/or PXL as necessary, including general training requirements, SOPs, and system and process related training
- Adhere to PXL and Client SOPs and processes
Skills and Education:
- BS/BA/MS/PhD with 2+ years clinical research experience
- Pharmaceutical experience beneficial but not required
- Therapeutic Area (TA)-specific experience beneficial
- Demonstrated oral and written communication skills
- Excel and Power Point (PP) experience required
#LI-REMOTE
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
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