Principal Scientist, Clinical Research
Core
Planning and directing clinical research activities for new or marketed medicines in the Atherosclerosis & Metabolism therapeutic area, managing the entire cycle of late-stage clinical development.
Role type
Principal Scientist, Clinical Research (Director level)
Builds
Late-stage clinical development programs for Atherosclerosis & Metabolism drugs
Domain
Pharmaceutical industry, Atherosclerosis & Metabolism
Required skills
Clinical trial design, Clinical development management, Regulatory reporting, Clinical study analysis, Publication of clinical findings, Investigator identification, Cross-functional collaboration
Preferred skills
Board certification in Cardiology/Endocrinology/Nephrology, Prior specific experience in clinical research, Publication record
Technologies
Clinical Trial Management Systems (CTMS), Electronic Data Capture (EDC), Statistical Analysis Software (SAS/R)
Responsibilities
Plan clinical trials based on development strategies; Monitor and manage conduct of ongoing or new clinical trials; Analyze and summarize clinical findings to support safety/efficacy decisions; Author development documents, presentations, and budgets; Facilitate collaborations with external researchers; Maintain awareness of scientific developments and establish communications with prominent investigators.
Seniority
Principal, hands-on IC with strategic oversight