Senior Clinical Director, Immunology
USA - New Jersey - Rahway
Job Description
The Senior Clinical Director (Sr. 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 Clinical 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
The Senior Clinical Director may:
Oversee the Clinical Directors and 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 Associate Vice-President/Vice-President and product development team lead in ensuring that appropriate corporate personnel is 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 Clinical 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.
To accomplish these goals, the Senior Clinical Director may:
Author detailed development documents, presentations, budgets, and position papers for internal and …
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Hybrid Hybrid work Hybrid work model On-site
Benefits/PerksBonus eligibility Diverse workplace Equal opportunity employer Flexible work Flexible work arrangements Hybrid work Hybrid work model Inclusion Inclusive environment Insurance Meetings Paid holidays Retirement benefits Separation benefits package Sick Days Team environment Vacation
Tasks- Analyze clinical findings
- Collaborate with experts
- Collaboration
- Directing clinical research activities
- Execution
- Innovation
- Manage clinical development
- Oversee clinical trials
- Planning
- Planning and directing clinical research activities
- Planning clinical trials
- Strategic Planning
Access Analysis Business Development Business Operations Clinical Clinical Development Clinical Development Strategies Clinical Research Clinical trials Clinical Trials Design Collaboration Collaborative relationships Commercial Commercialization Cross-functional Collaboration Data analysis Design Development Drug Development Education Execution Immunology Inclusion Innovation Interpersonal Investigational new drug applications Law Manufacturing Medicine Methodologies Monitoring Operational Operations Planning Product Development Project Management Regulatory Regulatory Affairs Regulatory Filing Research Research Methodologies Safety Scientific Writing Statistics Strategic planning Study Design Talent Acquisition Teams Therapeutic Areas
Experience8 years
EducationAS Associate Business DO Immunology M.D. M.D./Ph.D. Statistics
TimezonesAmerica/Anchorage America/Chicago America/Denver America/Los_Angeles America/New_York Pacific/Honolulu UTC-10 UTC-5 UTC-6 UTC-7 UTC-8 UTC-9