Assists the SM Study Lead and study team with the operational conduct of clinical studies (e.g., CTT minutes, clinical supplies planning/tracking, lab specimen tracking, imaging data reconciliation, status update reports, study closeout activities)
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
May interact with internal and external stakeholders (study sites, vendors, committees, etc.) in support of clinical study objectives
Minimum FTE Years of Experience
Pharmaceutical and/or clinical drug development experience
Oncology Therapeutic Experience
Demonstrated oral and written communication skills
Excel and Power Point experience required
Educational Requirements
BS/BA/MS/PhD with 2+ yrs clinical research experience
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Other
Industries
Pharmaceutical Manufacturing and Biotechnology Research
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