Principal Scientist at Merck managing clinical research activities in Immunology with focus on late-stage development. Overseeing clinical trials and collaborating with cross-functional teams.
Responsibilities
managing the entire cycle of clinical development, including determination of appropriate disease indications to pursue and subsequent study design
analyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy
supervising the activities of Clinical Scientists in the execution of clinical studies
maintaining awareness of scientific developments within his/her area of expertise
traveling on company business about twenty (20) percent of the time to manage future or ongoing clinical research projects
Requirements
M.D., D.O., M.D./PhD, or D.O./PhD required
Minimum of 5 years of clinical and/or development experience (academia, clinical medicine, and/or corporate clinical development)
Demonstrated record of scientific scholarship and achievement
Prior experience in design and execution of phase 2 or 3 clinical trials in rheumatologic diseases is preferred
Strong interpersonal skills, as well as the ability to work collaboratively in a cross-functional team environment
Benefits
medical, dental, vision healthcare and other insurance benefits (for employee and family)
retirement benefits, including 401(k)
paid holidays
vacation
compassionate and sick days
Job title
Principal Scientist, Clinical Research, Immunology
Principal Biostatistician Consultant at ClinChoice overseeing drug development statistical methodologies. Lead statistician for clinical studies in a hybrid work environment.
Part - time Clinical Research Coordinator for Penn's Center for Weight and Eating Disorders. Assist in industry - funded study on behavioral treatment effects and weight loss medications.
Clinical Research Coordinator supporting clinical research at University of Wisconsin. Collaborating with investigators and multidisciplinary teams to advance patient - centered research.
Managing clinical research coordinators for data quality and participant management at USF Health. Overseeing daily operations and coordinating with sponsors, ensuring compliance in clinical trials.
Clinical Research Coordinator managing the conduct of clinical trials at Emory University. Handling administrative activities and overseeing research project requirements and compliance.
Clinical Research Coordinator at MSK, focusing on data collection and integrity for cancer research projects. Collaborating with multidisciplinary teams and ensuring compliance with regulations.
Clinical Research Coordinator providing research support for grant projects at the University of Pennsylvania. Coordinating studies on decision - making tools for misophonia and pediatric anxiety treatment programs.
Clinical Research Coordinator managing phases of clinical trials under supervision at Perelman School of Medicine. Overseeing study operations, data management, and participant recruitment in a hybrid role.
Senior Principal Biostatistician providing statistical expertise across therapeutic areas in clinical development. Collaborating with study teams and overseeing analysis plans for vital projects.
Clinical Research Assistant supporting clinical trials and participant engagement in obesity care at knownwell, Inc. Responsible for patient - facing activities to ensure high - quality experience.