Senior Director, Pharmacological Sciences and Screening Technologies at Bristol Myers Squibb

, Virginia, United States -

Full Time

Start Date

Immediate

Expiry Date

01 Feb, 26

Salary

326768.0

Posted On

03 Nov, 25

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Pharmacology, Cell Biology, Biochemistry, Drug Discovery, In Vitro Assay Technologies, High-content Screening, Lab Automation, Leadership, Strategic Planning, Decision-making, Interpersonal Skills, Communication Skills, Collaboration, Innovation, Data Analysis, Molecular Profiling

Industry

Pharmaceutical Manufacturing

Description

Working with Us Challenging. 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. Discovery Biotherapeutics and Leads Discovery and Optimization (DBTx-LDO) is a multidisciplinary group of scientists providing critical molecular discovery, structural, functional, and mechanistic datasets to discover differentiated therapeutics. The Pharmacological Sciences and Screening Technologies team within DBTx-LDO plays a critical role in enabling lead discovery, molecular profiling, mechanistic differentiation and strategic insights for our drug discovery programs across a spectrum of therapeutic modalities. The team works collaboratively across adjacent functions including biology, protein sciences & biophysics, chemical biology, structural biology, translational biology, synthetic chemistry and computational chemistry for design and discovery of novel therapeutics. We seek a Senior Director, who will be accountable for oncology small molecule portfolio oversight, strategic vision setting and cross-geography (Cambridge, MA and Lawrenceville, NJ) collaborations to drive our exciting portfolio. The ideal candidate will be a passionate and experienced drug discovery scientist, and proven portfolio leader, collaborator and innovator. This is an on-site role based out of our Cambridge, MA site. Primary Responsibilities: Act as a subject matter expert, setting the strategic vision for the in vitro pharmacology team and ensuring the adoption of cutting-edge technologies and approaches. This includes staying current on the latest advancements in screening methodologies. Oversee and guide the design, optimization, and validation of cellular, biochemical and biophysical assays to support target identification, high-throughput screening (HTS), and lead optimization. Lead and manage hit generation, screening and molecular profiling activities for multiple drug discovery programs across different therapeutic areas. Work extensively in a matrix environment, collaborating with various departments such as medicinal chemistry, biology, computational sciences, and toxicology to advance drug discovery pipelines. Ensure the generation of high-quality data and use advanced software for data analysis, archiving, and interpretation to guide program decisions. Manage and lead a multi-disciplinary team of scientists across biochemistry and cellular pharmacology groups to impact and progress an exciting and innovative portfolio of novel therapeutics Supervise multiple PhD and advanced leaders and scientists within their teams. Management of technology infrastructure, future innovation and strategy. Foster a culture of transparency, innovation, career development and collaboration Qualifications: Passionate and innovative scientist with A Ph.D. in Pharmacology, Cell Biology, Biochemistry, or a related scientific discipline is typically required. Extensive industry experience (10+ years) in drug discovery, with a proven track record of successfully advancing programs from target concept to preclinical candidate selection. Deep expertise in diverse in vitro assay technologies, including cell-based and biochemical assays, high-content screening (HCS), and lab automation. Proven experience (8+ years) in a leadership role, including managing scientific teams and budgets. Strong strategic planning and decision-making abilities with an innovative mindset. Strong interpersonal, oral and written communication skills, highly effective in interacting with key internal and external stakeholders, and a commitment to working collaboratively across organizational boundaries to solve complex technical issues Passion for learning and advancing innovative approaches to drug discovery including proactive investigation of new techniques and capabilities, advanced software/hardware and innovative experimental approaches #LI-Onsite 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: $269,660 - $326,768 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 https://careers.bms.com/life-at-bms/. Benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following: Medical, pharmacy, dental and vision care. Wellbeing support such as the 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 support. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year’s holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Parental, 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. 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 adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility 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: https://careers.bms.com/california-residents/ Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. Data Privacy Link We’re creating innovative medicines for patients fighting serious diseases. We’re also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference.

Responsibilities

The Senior Director will set the strategic vision for the in vitro pharmacology team and oversee the design and optimization of assays to support drug discovery. They will manage a multi-disciplinary team and collaborate across various departments to advance drug discovery pipelines.