Leads in the development, evaluation, planning and execution of clinical studies
Ensures integrity and interpretation of study data of a clinical development program
Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings
Applies basic scientific expertise to support initiation and execution of clinical research and development studies
Maintains compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety
Exhibits strong analytical knowledge and skills to understand how study objectives and design impact data analysis

Bachelor’s Degree; Advanced degree or equivalent education/degree in life science/healthcare preferred (PhD/MD/PharmD/MSc)
≥ 8 years of pharmaceutical clinical drug development experience
Proven knowledge of the drug development process, Good Clinical Practice, study design, clinical research methodology & medical writing skills
Knowledge of clinical development process, regulatory requirements and ICH/GCP guidelines
Proven track in clinical trial process improvements
Considerable organizational awareness, including significant experience working cross-functionally

health and wellness programs (including medical, dental, vision, life, and disability insurance)
fitness centers
401(k) company match
family support benefits
equity awards
annual bonuses
paid time off
paid leaves (e.g., military and parental leave)

Senior Manager, Clinical Scientist, Hematology

Key skills