Executive Director, Clinical Scientist Program Lead - Neuroscience
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Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.
Clinical Scientist Program Lead The Clinical Scientist Program Lead reports through the Clinical Science function which provides scientific expertise necessary to design and deliver clinical studies and programs. This position leads a team and a complex scope of work to ensure high quality delivery of innovative protocols and data packages for CSRs and Regulatory Filings. The Program Lead oversees all clinical studies within assigned program(s).
Serves as a member of the Clinical Science Leadership Team and Global Program Team
Drives resource forecasting, talent development, succession planning and retention strategies
Defines and standardizes best practices and development opportunities for the scientist team
Builds a collaborative, supportive learning environment
Ensures and contributes to a consistent and high level of training for Clinical Scientists across the department with respect to relevant scientific data and knowledge, including SOPs and Working Practices
May serve as a delegate of Clinical Scientist Head as needed
Partners with the Clinical Development Lead accountable for the assigned program; supports activities required to develop clinical development and lifecycle management plans
Position Responsibilities: Leads a team or complex scope of work to ensure high quality delivery of innovative protocols and data packages for CSRs and Regulatory Filings
Oversees all clinical studies within assigned program(s) to ensure consistency across program(s)
Ensures high quality and timely delivery of protocols and data; implements quality assurance plans
Maintains an advanced understanding of the status of all trial activities within assigned Program
Provides scientific and clinical leadership to support the team; provide program/study/therapeutic area/skills training to team members
Attends Development Team meetings as needed
Leads resourcing and budget planning activities for team
Holds accountability for the performance and professional development of Clinical Scientist team
Leads proactive risk identification and mitigation plans; provides progress reports and risk assessment updates to Sr. Management
Reviews and approves clinical contributions to all trial documents / abstracts / publications
Reviews, audits, and presents data and information to internal leaders and external investigators
Serves as a key cross functional collaborator; represents the Clinical Scientist function in various process improvement initiatives and/or cross functional activities
Collaborates to support incoming asset and/or business development activities (i.e., due diligence)
Degree Responsibilities: Degree in Life Sciences (MD, PhD, Pharm D, MS, RN or other scientific field preferred)
Experience Requirements: 10+ years of experience in clinical science, clinical research, or equivalent
Extensive experience and demonstrated proficiency in managing direct/indirect employees and leading teams
Key Competency Requirements: Expertise in GCP/ICH, drug development process, study design, statistics, clinical operations
Recognized internally and externally as a Functional/Technical expert
Expert in analyzing, interpreting, and presenting data
Advanced knowledge and skills to help lead program specific data review, trend identification, data interpretation
Expertise in indication, therapeutic area, compound(s), competitive landscape and health authority requirements
Ability to act independently to identify/resolve and lead team towards resolving program level issues
Consistently recognized for strong critical thinking, problem solving, decision making skills
Advanced oral and written communication skills, including medical writing, presentations to large groups, facilitation of interactive discussions and 1:1 discussion with internal and external thought leaders
Demonstrated strong leadership presence
Expert financial acumen
Commitment to Quality
Adaptable / Flexible
Exhibits confidence and professional diplomacy, while effectively relating to people at all levels internally and externally
Promotes a culture of scientific excellence, multidisciplinary problem solving, teamwork, consistency, flexibility, execution, quality and effective communication
Anticipates needs, assesses and manages business and organizational risks.
Travel Required: Domestic and International travel may be required.
The starting compensation for this job is a range from $297,590-360,700 plus incentive cash and stock opportunities (based on eligibility).
Bristol Myers Squibb is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations and ongoing support in their roles. Applicants can request a reasonable workplace accommodation prior to accepting a job offer.
BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
BMS is an equal employment opportunity employer and complies with all applicable federal, state and local laws regarding recruitment, hiring and employment.
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- Location:
- Baltimore, MD, United States
- Job Type:
- FullTime
- Category:
- Bio & Pharmacology & Health