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Job Information
Intra-Cellular Therapies, Inc Executive Director, Clinical Development in Bedminster, New Jersey
Benefits Offered
401K, Dental, Life, Medical, Vision
Employment Type
Full-Time
“We deliver innovative treatments to improve the lives of individuals suffering from neuropsychiatric, neurologic and other disorders”
Intra-Cellular Therapies Inc. is a publicly traded biopharmaceutical company headquartered in New York City. Founded on Nobel-prize winning research, we launched our first commercial product in CNS in 2020 and received approval for an expanded indication in 2021. Currently celebrating our 22nd anniversary, we have a strong pipeline with projects in preclinical development stage through Phase III. We celebrate science, welcome curiosity, expect collaboration and demand integrity and respect in all we do, create and deliver.
About the Role:
The Executive Director, Clinical Scientist supports the Clinical Program Lead or functions as the Clinical Program Lead in the development of the Clinical Development Plan (CDP) and performs the relevant clinical tasks to ensure successful implementation of the CDP.
Responsibilities:
Clinical Tasks include but are not limited to the creation of the following:
Protocols/Amendments
Investigator Brochures
Informed Consent Forms
IND Annual Updates
Clinical Sections of the DSUR
Clinical Study Reports
Regulatory Submissions including Meeting Requests, Briefing Books, Efficacy and Safety Summaries
Scientific Publications
Clinical Tasks as they relate to Clinical Trials include but are not limited to:
Overseeing multiple studies across one or more compounds
Representing Clinical Development as a core member on a Clinical Trial Team
Assisting in the creation of Case Report Forms
Providing clinical input into clinical trial documents such as lab/ECG specifications and qualification methodology associated with rater training
Creation and review of training materials
Coordinating the development of Medical Monitoring and Clinical Oversight Plans
Performing clinical data review
Assessing protocol deviations
Assisting in the resolution of issues identified during clinical data and protocol deviation
Complete all company and job-related training as assigned within the required timelines.
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job.
Duties, responsibilities, and activities may change at any time with or without notice.
Requirements:
Bachelor’s Degree required
Advanced science degree (Masters or Doctorates) strongly preferred
Minimum 10 years of overall work experience or equivalent combination of experience and education
Minimum 8 years of clinical/research experience in the pharmaceutical/device industry preferred
Scientific knowledge and experience in a related therapeutic area preferred
Ability to travel at least 30%
Ability to work in a team setting as well as function as an individual contributor
Ability to work efficiently and under tight timelines
Ability to communicate effectively
Ability to be flexible in an ever-changing environment
Ability to think strategically and be able to anticipate problems before they occur
Ability to be proactive in finding solutions to issues
Proficient in Microsoft office (word, excel, PowerPoint)
Must be able to perform all essential functions of the position, with or without reasonable accommodation
Intra-Cellular Therapies is an Equal Employment Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, protected veteran status, disability or any other legally protected status.
Executive Director, Clinical Development - Base Salary Range $250,000 - $280,000
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Intra-Cellular Therapies, Inc
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