Senior Principal Scientist, Clinical Research, Immunology

Benefits

Qualifications

• •M.D., D.O., M.D./PhD, or D.O./PhD.
• •Experience in the design and/or execution of phase 2 or 3 clinical trials specifically in Immunology (Rheumatology, Gastroenterology or Dermatology)
• •Minimum of 3 years of clinical medicine experience
• •Minimum of 5 years of industry experience in drug development
• •Demonstrated record of scientific scholarship and achievement
• •Strong interpersonal skills, as well as the ability to work collaboratively in a cross-functional team environment
• •Clinical Development, Clinical Medicine, Clinical Research Management, Clinical Studies, Clinical Trial Development, Clinical Trials, Dermatology, Drug Development, Gastroenterology, Inflammatory Bowel Diseases, Pharmaceutical Industry, Regulatory Compliance, Rheumatology
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Responsibilities

• •Principal Scientist) has primary responsibility for the strategic planning and directing clinical research activities involving investigational compounds in Immunology
• •With a focus on late-stage development, the Senior Clinical Director will manage the entire cycle of clinical development, including determination of appropriate disease indications to pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication
• •Specifically, The Senior Director May Be Responsible For:
• •Evaluating pre-clinical and translational work for the purpose of generating the early clinical development plan and Investigational New Drug applications
• •Providing clinical development support of business development assessments of external opportunities to grow the Immunology Pipeline
• •Developing clinical development strategies for investigational drugs and planning clinical trials (design, operational plans, settings) based on these clinical development strategies
• •Monitoring and managing the conduct of ongoing or new clinical trials for investigational drugs
• •Analyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication; and
• •Participation in internal and joint internal/external research project teams relevant to the development of new compounds
• •Supervise the activities of Clinical Scientists in the execution of clinical studies
• •Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects; and assist the Executive Director in ensuring that appropriate corporate personnel are informed of the progress of studies of our company and competitors' drugs and internal and external expert opinion on scientific questions relevant to his/her areas of responsibility
• •The Senior Director is responsible for maintaining a strong scientific fund of knowledge by:
• •Maintaining awareness of scientific developments within his/her area of expertise, in terms of new scientific findings, research methodologies
• •Identification of scientifically and operationally strong investigators who can assist in the development of our company's investigational drugs in Immunology
• •Establishing collaborative relationships with external experts in Rheumatology, Gastroenterology, Dermatology, and pulmonary disease, particularly those whose research focus and expertise can inform and assist the evaluation of the company's investigational drugs
• •Attending appropriate scientific meetings to maintain his or her competency and to maintain awareness of research activities in his/her area of responsibility
• •Author detailed development documents, presentations, budgets, and position papers for internal and external audiences
• •Facilitate collaborations with external researchers around the world
• •Travel on company business about twenty (20) percent of the time to manage future or ongoing clinical research projects
• •This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely
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