Executive Director, Clinical Scientist Program Lead - Neuroscience
Executive Director, Clinical Scientist Program Lead - Neuroscience
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Job Description
Working with Us
Challenging. Meaningful. Life-changing. Those arent 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. Youll 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. Read more: 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 Page 2
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 jobis a range from $00 plus incentive cash and stock opportunities (based on eligibility).
The starting pay rate takes into account characteristics of the job such as required skills and where the job is performed.
Final individual compensation will be decidedbased on demonstratedexperience.
Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits please visit subject to the terms and conditions of the applicable plans then in effectand may include the following: Medical pharmacy dental and vision care. Wellbeing supportsuch asthe BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability life insurance supplemental health insurance business travel protection and survivor -life programs include paid national holidays and optional holidays Global Shutdown Days between Christmas and New Years holiday up to 120 hours of paid vacation up to two (2) paid days to volunteer sick time off and summer hours caregiver bereavement and military leave. Family care services such as adoption and surrogacy reimbursement fertility/infertility benefits support for traveling mothers and child elder and pet care resources. Other perks like tuition reimbursement and a recognition program.
If you come across a role that intrigues you but doesnt perfectly line up with your resume we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
Uniquely Interesting Work Life-changing Careers
With a single vision as inspiring as Transforming patients lives through science every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture promoting global participation in clinical trials while our shared values of passion innovation urgency accountability inclusion and integrity bring out the highest potential of each of our colleagues.
On-site Protocol
BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential site-by-design field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles onsite presence is considered an essential job function and is critical to collaboration innovation productivity and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application or in any part of the recruitment process direct your inquiries to . Visit to access our complete Equal Employment Opportunity statement.
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.
If you live in or expect to work from Los Angeles County if hired for this position please visit this page for important additional information: data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
Required Experience:
Director
Employment Type
Full-Time
