Senior Manager, Global Clinical Scientist – Neuroscience

Bristol Myers Squibb

. Provide scientific expertise to design and deliver clinical studies and programs .

Posted 9/21/2026full-timeUnited StatesSenior💰 $150,770 - $182,701 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in designing and executing clinical studies, with a strong understanding of GCP/ICH guidelines and the drug development process. Proficient in medical writing, data monitoring, and project management, while effectively collaborating with cross-functional teams and external partners.

Highest-signal resume keywords

Clinical Trial DesignGCP/ICH KnowledgeMedical Writing SkillsData Review and MonitoringProject Management Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Study DesignProtocol DevelopmentData Review PlansStatistical AnalysisClinical OperationsLiterature ReviewClinical Document SubmissionCRA Training DevelopmentTrend IdentificationRegulatory Document Preparation

Soft Skills

Detail-OrientedCritical ThinkingProblem-SolvingAdaptabilityCollaboration

Tools & Technologies

Microsoft WordMicrosoft ExcelMicrosoft PowerPointData Review ToolsReport-Generating Tools

Industry Keywords

Life SciencesClinical TrialsDrug DevelopmentClinical OperationsGDO Protocol Management

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Provide scientific expertise to design and deliver clinical studies and programs
Design and execute assigned clinical trial activities
Work closely with clinical team members to conduct assigned projects
Serve as Clinical Trial Lead for one or more trials as applicable
Lead or support trial-level activities under necessary supervision
Co-lead study team meetings with the GDO protocol manager
Collaborate with cross-functional study team members and external partners such as KOLs
Seek out and enact best practices with instruction
Provide regular and timely updates to management
Develop protocol and ICF documents and amendments
Present documents to governance committees and development team meetings
Conduct literature reviews
Submit clinical documents to the TMF
Develop site and CRA training materials and present them at SIVs and investigator meetings
Review clinical narratives
Monitor clinical data for specific trends
Develop Data Review Plans with Data Management
Ensure CRF design supports protocol-aligned data collection with Data Management and Programming
Submit clinical contributions to CSRs and clinical portions of regulatory documents and submissions

Requirements

What you’ll need

Degree in Life Sciences (MD, PhD, Pharm D, MS, RN or other scientific field preferred)
Basic knowledge of GCP/ICH, drug development process, study design, statistics, and clinical operations
Ability to understand assigned protocol(s) and their requirements
Basic knowledge to support program-specific data review and trend identification
Intermediate medical writing skills and medical terminology
Basic planning/project management skills
Detail-oriented with commitment to quality
Basic knowledge of disease area, compound, and current clinical landscape
Basic knowledge of data monitoring committees, dose review teams, and independent response adjudication committees
Intermediate critical thinking and problem-solving skills
Adaptability and flexibility to adjust to multiple demands and shifting priorities
Intermediate skills in Microsoft Word, Excel, PowerPoint, and data review tools such as Pt Profiles and report-generating tools
Domestic and international travel may be required

Benefits

Comp & perks

Comprehensive benefit plans including wellbeing support, retirement and financial protection benefits, and medical, dental, vision, life and disability insurance offerings
Flexible Time Off (FTO) for U.S.-based exempt employees, subject to manager approval
11 paid company holidays each year
160 hours of paid vacation annually for eligible new hires
3 optional holidays for eligible employees
Paid sick leave
Up to two paid volunteer days per year
Summer hours flexibility
Medical, personal, parental, caregiver, bereavement, and military leaves of absence
Annual Global Shutdown between Christmas Day and New Year's Day