Bristol Myers Squibb

Director

• Acquires and utilizes knowledge of clinical trial design to develop or oversee development of specific study concept synopses and protocols.
• Participates in protocol review discussions concerning scientific and procedural aspects of study design.
• In collaboration with Medical Writing and Clinical Operations, prepares study protocols, amendments, specific sections of study manuals and Investigator meeting materials, and other documents as needed with appropriate guidance and supervision.
• Works with medical writing vendors to coordinate writing and reviewing of protocols, ICFs, IBs and other clinical trial documents as needed.
• Contributes to the design, development, and review of CRFs, Data Management Manuals, and Data Analysis Plans.
• Reviews ongoing clinical data and interacts with CROs to ensure data queries are addressed and data is clean for database locks.
• Organizes and oversees Data Review Committee meetings, including preparation of slides and other review and meeting materials.
• With MD supervision, addresses questions regarding scientific and related procedural issues from Investigators.
• Participates in Site initiation visits and study start up activities.
• Establishes and maintains positive relationships with clinical trial investigators and site staff.
• Contributes to interactions with key thought leaders in gaining input on protocols and study designs and strategic direction.
• Contributes to the preparation and/or review of data listings, summary tables, study results, manuscripts, and scientific presentations.
• Assists in the preparation/review of INDs, regulatory documents, IND annual report/DSURs, Investigator Brochures, and NDAs/MAAs.
• Supports priorities within functional area.
• Anticipates moderately complex obstacles within a clinical study and, with guidance, implements solutions.
• May be asked to coordinate teams and provide direction.
• May lead two or more specific components of departmental strategic initiatives.
• Able to enter a new therapeutic area and summarize scientific information that is available in published literature to integrate into new study development.
• Excellent verbal and written communication skills and interpersonal skills are required to maintain working relationship with team members to ensure scientific integrity of clinical studies.
• May be sought out for advice by others within the company to help make better decisions and resolve moderately complex problems.
• Applies AI to improve team execution and decision‑making.

Director, Clinical Science

Therapist

• Provide technical support on RM/SUS to the drug product manufacturing team.
• Strong focus on critical raw material issue resolution.
• Lead the technical support pillar of Materials Science by facilitating Material Health Committee meetings to intake new issues and continuous improvements, monitor KPIs, align functional area ownership, and coordinate resolution.
• Collaborate cross-functionally to execute risk mitigations and initiatives to improve the quality and robustness of existing RM/SUS.
• Lead/support projects for qualification of new or alternate sourcing efforts for RM/SUS.
• Build strategy for lifecycle changes and raw material robustness.
• Collaborate with Manufacturing, Process Development, Analytical R&D, Quality Operations, MSAT network to ensure raw material oversight.
• Support internal and external manufacturing site(s) on investigations related to RM/SUS.
• Provide necessary technical analysis to support impact assessments for investigations and change control (internal and supplier change notification).
• Facilitate the development of appropriate mitigations and corrective actions.
• Support supplier quality assurance (SQA) on vendor management including change controls, audits, deviations, and Quality Risk Management (QRM) programs.
• Lead/support technical diligence and audits to RM/SUS supplier sites with cross-functional teams.
• Support other members of the team with deviations, change control, and project support for RM/SUS for late stage clinical/commercial CT/vector.
• Author the RM/SUS section of the filing for new regulatory submissions.
• Author responses for Information Requests (IR) from regulatory bodies.

Scientific Associate Director – Cell Therapy Materials Science

• Identify Key Opinion Leaders (KOLs), and establish and maintain scientific relationships with KOLs, connecting KOLs in academic and community centers.
• Act as primary liaison to investigators interested in developing and performing investigator-initiated research.
• Develop and execute geography-specific Field Medical and KOL Interaction plans based on therapeutic area objectives and KOL needs.
• Provide clinical presentations and information in response to unsolicited questions (as appropriate) in academic, community, and healthcare provider setting in both group and one-on-one situations.
• Collaborate with the Clinical organization to enhance patient enrollment in BMS-sponsored clinical trials by identifying appropriate clinical trial sites and interacting with investigators in ongoing studies.
• Provide scientific support at medical congresses.
• Provide timely feedback/information on emerging clinical/scientific teams and opportunities to internal stakeholders.

Medical Science Liaison, Cell Therapy

• Responsible for assessing, cultivating, and managing customer relationships across a broad set of stakeholders within assigned accounts.
• Responsible for the development of a customized site-specific account plan coordinating the deployment of resources to meet customer needs and ensure a seamless and differentiated customer experience.
• Serve as the main point of contact for designated accounts and collaborate with cross-functional partners to create a streamlined, organized interface between account stakeholders and all field-facing colleagues.
• Navigate complex account environments and understand the needs/issues of account stakeholders at all levels and drive to solutions that address the needs.
• Collaborate and communicate regularly with cross-functional partners to support the referral of appropriate patients to the treatment centers.
• Maintain and continuously develop both disease and product-specific knowledge.
• Actively gains customer insights and provides timely feedback to cross-functional partners and Area Business Manager regarding account business trends, changes in the therapeutic landscape, performance, industry issues and business opportunities and risks.
• Ensure compliance with all laws, regulations and policies that govern the conduct of cell therapy activities.

Account Manager, Cell Therapy

Artificial Intelligence

• Develop and Deploy Machine Learning Pipelines: Apply expertise in machine learning to create, implement, and optimize end-to-end pipelines that address critical business problems in clinical study design and execution.
• Automate workflows to process and analyze complex datasets, such as clinical trial protocols, real-world evidence, and patient recruitment data.
• Ensure the scalability, reliability, and robustness of deployed machine learning solutions for real-time decision support.
• Drive Stakeholder Engagement and Collaboration: Partner with cross-functional teams, including IT, medical, development, and biostatistics groups, to co-develop AI-driven solutions aligned with business priorities.
• Act as liaison between technical teams and non-technical stakeholders, ensuring alignment on objectives and fostering a collaborative environment for successful solution delivery.
• Manage AI Product Lifecycle: Oversee the lifecycle of AI products, from ideation and development to deployment and monitoring.
• Conduct post-deployment analysis to measure the impact of implemented solutions and identify areas for continuous improvement.

Senior Manager, Analytical AI Clinical Development

Supply Chain

• Lead and ensure successful prioritization, deployment, and execution of GSC Strategic Projects, Book of Work, and Global Initiatives.
• Oversee Business Development initiatives, including divestitures, integrations, alliance agreements, and network changes.
• Act as the primary Point of Contact for GSC in Business Development initiatives, ensuring matrixed coordination throughout all phases.
• Represent GSC during due diligence and preparation phases, ensuring appropriate impact assessments are made and incorporated.
• Create and maintain the GSC knowledge playbook and introduce standard work.
• Deploy GSC strategy across pillars, driving transformation and ensuring cross-GSC and PDS alignment.
• Develop strong relationships with partners and build successful cross-functional teams, balancing resources with competing BMS global objectives.

Senior Director, Global Supply Chain Transformation

• Identify, establish and maintain scientific relationships with Key Opinion Leaders (KOLs)
• Act as primary liaison to investigators interested in developing and performing investigator initiated research.
• Develop and execute geography-specific Field Medical and KOL Interaction plans based on therapeutic area objectives and KOL needs.
• Partner with other BMS MSL teams to achieve CTAI objectives and goals with rheumatologists and hematologists
• Support patient education initiatives, serving as subject matter expert on BMS pipeline and investigational therapies
• Provide clinical presentations and information in response to unsolicited questions (as appropriate) in academic and healthcare provider settings in both group and one-on-one situations.
• Collaborate with the Clinical research and development organization to enhance patient enrolment in BMS-sponsored clinical trials by identifying appropriate trial sites and actively interacting with participating investigators.
• Provide scientific support at National, Regional and Local medical congresses/meetings.
• Capture and provide timely feedback/insights to internal stakeholders regarding the cell therapy and autoimmune treatment landscape for strategy development.

Medical Science Liaison, Cell Therapy Autoimmune

• Identify, establish and maintain scientific relationships with Key Opinion Leaders (KOLs)
• Act as primary liaison to investigators interested in developing and performing investigator initiated research.
• Develop and execute geography-specific Field Medical and KOL Interaction plans based on therapeutic area objectives and KOL needs.
• Partner with other BMS MSL teams to achieve CTAI objectives and goals with rheumatologists and hematologists
• Support patient education initiatives, serving as subject matter expert on BMS pipeline and investigational therapies
• Provide clinical presentations and information in response to unsolicited questions (as appropriate) in academic and healthcare provider settings in both group and one-on-one situations.
• Collaborate with the Clinical research and development organization to enhance patient enrollment in BMS-sponsored clinical trials by identifying appropriate trial sites and actively interacting with participating investigators.
• Provide scientific support at National, Regional and Local medical congresses/meetings.
• Capture and provide timely feedback/insights to internal stakeholders regarding the cell therapy and autoimmune treatment landscape for strategy development.

• Identify, establish and maintain scientific relationships with Key Opinion Leaders (KOLs)
• Act as primary liaison to investigators interested in developing and performing investigator initiated research.
• Develop and execute geography-specific Field Medical and KOL Interaction plans based on therapeutic area objectives and KOL needs.
• Partner with other BMS MSL teams to achieve CTAI objectives and goals with rheumatologists and hematologists.
• Support patient education initiatives, serving as subject matter expert on BMS pipeline and investigational therapies.
• Provide clinical presentations and information in response to unsolicited questions (as appropriate) in academic and healthcare provider settings in both group and one-on-one situations.
• Collaborate with the Clinical research and development organization to enhance patient enrolment in BMS-sponsored clinical trials by identifying appropriate trial sites and actively interacting with participating investigators.
• Provide scientific support at National, Regional and Local medical congresses/meetings.
• Capture and provide timely feedback/insights to internal stakeholders regarding the cell therapy and autoimmune treatment landscape for strategy development.

QA Engineer

• Define and implement a global harmonization roadmap for GPQ standards, processes, and tools across all sites and programs.
• Lead a global matrix team of product quality experts, influencing without direct authority to achieve alignment across products.
• Drive lifecycle platform strategies for Integrated Control Strategy (ICS), Stability, analytical lifecycle management, jurisdictional control and specification strategy.
• Harmonize product quality risk assessment (PQRA) methodologies and robustness metrics across programs.
• Ensure all harmonized processes meet global regulatory requirements and support inspection readiness.
• Partner with CTTO, QA/QC, Regulatory, and Manufacturing Operations to embed harmonized standards into operational workflows.
• Foster a culture of innovation, agility, collaboration, and inclusion within the quality team, while maintaining a strong compliance and quality mindset.
• Establish and meet ambitious quality performance and compliance metrics in alignment with business and financial objectives.
• Lead internal and external governance meetings, including steering committees and partner collaborations, to ensure alignment and proactive quality management.

Director, Clinical Science

Scientific Associate Director – Cell Therapy Materials Science

Medical Science Liaison, Cell Therapy

Account Manager, Cell Therapy

Senior Manager, Analytical AI Clinical Development

Senior Director, Global Supply Chain Transformation

Medical Science Liaison, Cell Therapy Autoimmune

Medical Science Liaison, Cell Therapy Autoimmune

Medical Science Liaison, Cell Therapy Autoimmune

Medical Science Liaison, Cell Therapy Autoimmune

Medical Science Liaison, Cell Therapy Autoimmune

Medical Science Liaison, Cell Therapy Autoimmune

Senior Director, Product Quality Engineering

Medical Science Liaison, Cell Therapy Autoimmune

Medical Science Liaison, Cell Therapy Autoimmune