Cllinical Scientist Program Lead

Vor 7 Tagen


Boudry, Schweiz Bristol Myers Squibb Vollzeit

At Bristol Myers Squibb, we are inspired by a single vision - transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.

**Functional Area Description**

The Clinical Scientist Program Lead reports through the Clinical Science function which provides scientific expertise necessary to design and deliver clinical studies and programs.
**Position Summary / Objective**
- Partners with Clinical Scientist Head to plan, lead, and advance programs and talent
- Serves as a member of the Clinical Science Leadership Team and Development Team
- Supports 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 Requirements**
- Degree in Life Sciences (MD, PhD, Pharm D, MS, RN or other scientific field preferred)
**Experience Requirements**
- 15+ years of experience in clinical science, clinical research, or equivalent
- Experience working on assets for malignant and non-malignant hematological disorders including myelodysplastic syndrome, myelofibrosis, thalassemia, etc
- 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
- Advanced ability to analyze, interpret, and present data
- Advanced knowledge and skills to support program specific data review, trend identification, data interpretation
- Expertise in of 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
- 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.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competit



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