Associate Director, Global Clinical Science - Neuroscience

Working with UsChallenging. 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. Read more: careers.bms.com/working-with-us.The Associate Director, Global Clinical Science reports through the Clinical Science function which provides scientific expertise necessary to design and deliver clinical studies and programs.Position Summary / ObjectiveResponsible for implementation, planning, and execution of assigned clinical trial activities. Serves as Clinical Trial Lead for one or more trialsSuccessfully leads, plans, and executes trial level activities for multiple trials with minimal to moderate level of supervisionProvides scientific and clinical leadership to team of supporting Clinical Scientists (matrix leadership)Co-Leads study team meetings in partnership with GDO protocol manager; and collaborate with cross functional study team membersMay support clinical development planning (collaboration with Clinical Development Lead/Clinical Trial Physician for provision and analysis of data to support future planning)Position ResponsibilitiesMaintain a thorough understanding of assigned protocols and protocol requirements; educate supporting team membersPlan and lead the implementation all study startup/conduct/close-out activities as applicableEvaluate innovative trial designs (collaboration with Medical Monitor/Clinical Development Lead)Protocol and ICF development process with minimal guidance; including writing, reviewing, adjudication/resolution of cross functional comments and ensuring high clinical quality (collaboration with Medical Writing)Site-facing activities such as training and serving as primary contact for clinical questionsActivities related to data generation and validation, including CRF design, clinical data review/query resolution; ensure consistent, quality data review by supporting CS teamClinical data trend identification; provide trends and escalate questions to Medical MonitorDevelop clinical narrative plan; review clinical narrativesProvision of information required by Protocol Manager for development of trial budget, CRO scope of work, etc.Review development of site and CRA training materials and presentation at SIV and Investigator meetings and support on Study committee (e.g., DMC) activitiesDrafting/review and validation of clinical study reports (CSRs) and clinical portions of Regulatory Documents (e.g., IB, DSUR, regulatory responses)Collaborate and serve as primary liaison between external partners for scientific adviceDegree RequirementsDegree in Life Sciences (MD, PhD, Pharm D, MS, RN or other scientific field preferred)Experience Requirements5+ years of experience in clinical science, clinical research, or equivalentProficient knowledge of GCP/ICH, drug development process, study design, statistics, clinical operationsProficient knowledge and skills to support program specific data review, trend identification, data interpretationKnowledge of the establishment and operation of data monitoring committees, dose review teams, and independent response adjudication committeesKey Competency RequirementsExcellent verbal, written, communication and interpersonal skillsMust be able to effectively communicate and collaborate across functions and job levelsAbility to assimilate technical information quicklyRoutinely takes initiativeDetail-orientedStrong sense of teamwork; ability to lead team activitiesProficient in Medical Terminology and medical writing skillsProficient knowledge of the disease area(s), KOLs, indication(s), compound(s) under study (including MOA, PK/PD, biomarker & safety profile)Proficient critical thinking, problem solving, decision making skillsUnderstanding of functional and cross-functional relationshipsCommitment to QualityAdaptable / Flexible - willing and able to adjust to multiple demands and shifting priorities as well as an ability to meet day-to-day challenges with confidence and professionalismProficient planning/project management skills (ability to develop short to mid-range plans that are realistic and effective in meeting goals)Proficient in Microsoft Word, Excel, PowerPoint, Electronic Data Capture (e.g., RAVE), J-Review or similar data reporting toolsTravel RequiredDomestic and International travel may be required.If you come across a role that intrigues you but doesn’t 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.Compensation Overview:Cambridge Crossing: $211,910 - $256,789 Madison - Giralda - NJ - US: $184,270 - $223,294 Princeton - NJ - US: $184,270 - $223,294 The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit h