Director, Data Science, Groups Job at Meta (Menlo Park)

Executive Director, Curio Science

The Executive Director of Curio Science will lead with a growth-first mindset, d...

Location

United States

Salary:

180000.00 - 200000.00 USD / Year

Vaniam Group

Expiration Date

Until further notice

Requirements

Bachelor’s degree required (advanced degree in business, life sciences, or communications preferred)
Minimum 10+ years of agency experience required, ideally within healthcare communications or medical marketing
At least 6+ years of experience in managing cross-functional teams, including expertise in recruitment operations, program logistics, and compliance-sensitive initiatives
Proven track record in driving business growth through innovation, client engagement, and operational collaboration
Preferred experience in healthcare insights and analytics
Entrepreneurial and innovative mindset with deep expertise in scaling subscription-based, insights-driven, or other growth-focused services
Demonstrated ability to lead diverse teams within a fast-paced, client-centered agency environment, with a focus on cross-functional collaboration
Expertise in recruitment strategies, metrics tracking, and pipeline scalability to grow HCP and institutional networks effectively
Strong familiarity with industry regulations such as the Sunshine Act, PhRMA guidelines, and compliance-sensitive operations tied to HCP payments and events
Data-driven decision-maker with exceptional organizational and analytical skills

Job Responsibility

Lead and manage Curio Science teams, providing strategic direction and ensuring operational excellence in all aspects of execution and delivery
Drive sustainable growth by fostering a culture of performance, accountability, and collaboration across all team operations
Support the growth and execution of subscription-based models, third-party insights services, and other innovative offerings, ensuring alignment with Curio Science’s strategic growth priorities and competitive positioning as well as maintain compliance
Analyze industry trends, emerging market opportunities, and competitive activity to proactively adapt strategies and secure leadership in the space
Strengthen Curio Science’s footprint by cultivating relationships with healthcare professionals (HCPs), institutions, industry stakeholders, academic practices, and Key Opinion Leaders (KOLs) across multiple therapeutic areas to deepen networks and expand partnerships
Provide oversight for medical communications program services teams, including meeting logistics, event execution, and compliance-sensitive workstreams such as Sunshine Act/Open Payments reporting
Align Program Services strategies and logistics planning with Vaniam Group priorities, ensuring seamless integration across teams and initiatives as well as integration of AI into those workstreams
Offer high-level support and guidance to Program Services for efficient operational execution and resource management
Oversee recruitment efforts reporting into Curio Science, to achieve key targets in HCP and institutional representation
Develop innovative recruitment campaigns, expanding footprint and engagement across practices, healthcare institutions, and academic centers

What we offer

100% remote environment with opportunities for local meet-ups
Positive, diverse, and supportive culture
Passionate about serving clients focused on Cancer and Blood diseases
Investment in you with opportunities for professional growth and personal development through Vaniam Group University
Health benefits – medical, dental, vision
Generous parental leave benefit
Focused on your financial future with a 401(k) Plan and company match
Work-Life Balance and Flexibility
Flexible Time Off policy for rest and relaxation
Volunteer Time Off for community involvement

Fulltime

Director Data Science

Amgen is expanding its global Biostatistics capabilities, with Amgen India (AIN)...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree and 10 years of Scientific and/or work-related experience
Master’s degree and 18 years of Scientific and/or work-related experience
Bachelor’s degree and 20 years of Scientific and/or work-related experience
MS or PhD in Data Science, Computer Science, Informatics, Statistics, Mathematics, Life Sciences, or similar field
10+ years of experience in clinical research and/or predictive analytics
Wide experience analyzing clinical trial, real world, and/or ‘omics data
Specialization in few ML areas ( NLP, Vision, Bayesian Modelling) and provide mentorship to different groups
Led big projects in previous or current roles
Experience of working with Senior Leadership

Job Responsibility

Collaborate with Sr. Directors Data Science/Engineering to set the technical vision, mission, and strategy for the CfDA Data Science group
Continually assess and introduce cutting-edge technologies, ideas, and state-of-the-art ML/AI methodologies for clinical development
Lead the execution of major data science projects, providing technical guidance and ensuring high-quality deliverables
Run cross functional project teams and delivers project end to end
Mentor and guide a team of data scientists, fostering technical growth and expertise
Collaborate closely with IS/other analytical organizations to ensure alignment on analytical platforms and data strategies
Coordinate with Data Science Head to help set vision, mission, and strategy for CfDA Data Sciences group
Identify high-value projects across Clinical Development
Advise Data Science Head during prioritization, resource, and funding decisions
Establish annual goals for CfDA Data Scientists

What we offer

Vast opportunities to learn and move up and across our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Director, Group Lead, Data Surveillance, Clinical Data Sciences

As part of the Clinical Data Sciences group, an integral delivery unit within th...

Location

India , Chennai

Salary:

Not provided

Pfizer

Expiration Date

Until further notice

Requirements

Bachelor’s Degree. Degree in Life Sciences, Informatics, Computer Science, Statistics, or related business degree with equivalent experience preferred
Demonstrated relevant experience in a pharmaceutical, biotech, Contract Research Organization (CRO), or Regulatory Agency with an emphasis on building data collection and assimilation solutions
Demonstrated experience managing complex projects and developing successful partnerships within and across functional areas
Demonstrated successful experience in all relevant clinical trial activities in a Bio Pharmaceutical or CRO setting
Working knowledge of all phases of clinical trials and multiple indications and/or therapeutic areas. Ability to assess and determine study requirement from protocol review
Strong Project and Risk Management
Understanding of regulatory requirements and relevant data standards
Strong communication, decision-making, influencing, negotiation, and project management skills
Technical skill and experience using relational databases and data visualization tools, e.g. Spotfire, JReview

Job Responsibility

Define and drive global strategies, initiatives, processes, and standards to ensure consistent, efficient, and quality processes to deliver high quality clinical data
Plan and execute communication plans & methods to ensure customer satisfaction and enable improvements to be implemented during the course of a project
Develop charters, resource utilization and project plans to achieve CDS specific goals
Develop people, including recruitment, retention, and career development and performance management
Able to resolve conflicts, influence and communicate cross-functionally with key stakeholders and customers
Provides administrative and central monitoring technical and process oversight of teams
Implements organizational design and develop succession planning for RBM in collaboration with other functional leaders
Oversee all technical aspects required to set up and test study level Risk-based Monitoring system
Anticipates, oversees and influences change to position efficient, high-quality implementation of required data flows to incorporate internal and external data sources into Pfizer informatics environment ensuring operational delivery and traceability from source. Ensures appropriate process and documentation are in place to support inspection readiness
Act as the key scientific and technical central monitoring expert

Fulltime

Senior Director, Data Science

The Senior Director of Data Science will set and drive the enterprise-wide visio...

Location

United States

Salary:

135700.00 - 278300.00 USD / Year

One Call

Expiration Date

Until further notice

Requirements

Bachelor’s degree (B.A. or B.S.) in Statistics, Mathematics, Computer Science, or related quantitative field
advanced degree preferred
10+ years of experience in data science, with several years in senior leadership roles managing larger teams and enterprise-level projects
Strong problem-solving skills with an emphasis on product development and business impact
Experience using statistical computer languages (R, Python, SQL, etc.) to manipulate data and draw insights from large data sets
Knowledge of a variety of machine learning techniques (clustering, decision tree learning, artificial neural networks, etc.) and their real-world advantages/drawbacks
Knowledge of advanced statistical techniques and concepts (regression, properties of distributions, statistical tests and proper usage, etc.) and experience with applications
Excellent written and verbal communication skills for coordinating across teams and influencing senior stakeholders
A drive to learn and master new technologies and techniques
Demonstrated ability to develop and drive strategies that enhance business performance, with proven results at the enterprise level

Job Responsibility

Set and drive the enterprise-wide data science vision, ensuring alignment with executive leadership and long-term business objectives
Architect and oversee technical strategy for all data science initiatives, championing innovation in AI/ML methodologies and platforms
Lead the design, development, and deployment of ML models, focusing on advanced techniques such as Natural Language Processing (NLP), generative AI, and automation
Own the development and governance of a modern data platform for all data consumers
Lead LLM integration projects to automate manual processes and improve operational efficiency
Stay current with emerging technology trends and represent the organization in external forums, conferences, and industry groups
Collaborate with senior leaders across IT, Product, Operations, Marketing, and other business units to identify and execute high-impact, cross-functional data initiatives
Drive AI solutions for automation, decision intelligence, and enhanced customer experience
Translate complex data insights into actionable business strategies and measurable outcomes
Manage larger, multi-disciplinary teams, mentoring and developing future leaders within the data science organization

What we offer

Remote Work: We are a remote-first company, and almost all positions receive the flexibility of working from home
Generous Time Off: Besides 8 company holidays and 2 personal days every year, all colleagues receive a minimum of 18 days of paid time off
Comprehensive Benefits Package: Including medical, dental, vision, and pet insurance
401(k) matching program
and company-paid life insurance and short and long-term disability coverage
Supportive Services: We offer a Colleague Assistance Program that provides free counseling and financial services, and our One Call Foundation, a non-profit arm of our company, provides colleagues financial assistance during times of unexpected hardships

Fulltime

Associate Director, Data Governance, Standards & Quality, RIM&DO

You will lead data governance, standards and quality activities for Regulatory I...

Location

India; Poland; United Kingdom , Bengaluru; Poznan; London

Salary:

288000.00 - 480000.00 PLN / Year

GSK

Expiration Date

Until further notice

Requirements

Bachelor’s degree in data, life sciences, IT, engineering or related field, or equivalent experience
10+ years’ experience in data governance, data management, or regulatory information management
Hands-on experience defining and implementing data standards, taxonomies or metadata models
Experience with data quality tooling, metrics and remediation approaches
Strong stakeholder management and ability to influence in matrixed teams
Excellent communication skills in English
ability to simplify complex topics for diverse audiences

Job Responsibility

Define, implement and maintain data governance frameworks, standards and policies for regulatory information
Drive data quality programs, including data profiling, remediation plans and ongoing monitoring
Partner with Regulatory, IT and product teams to embed standards, and data governance and quality by design into systems, processes, and change controls
Lead cross-functional working groups to resolve data issues and improve end-to-end data flows
Advocacy throughout Regulatory and R&D on rolling out data governance frameworks at operational and strategic levels
Develop and report meaningful metrics and dashboards to show data quality, risks and progress
Coach and influence stakeholders to adopt data standards and operate with shared accountability
Own the design and deployment of data quality monitoring solutions, data standards, and data cataloguing for regulatory information assets
Run data stewardship and governance meetings and ensure decisions are tracked and implemented
Assess data risks and coordinate remediation with clear timelines and owners

What we offer

Competitive base salary
Annual bonus based on company performance
Flexible working options available for most roles
Learning and career development
Access to healthcare & wellbeing programmes
Employee recognition programmes
Private healthcare
Additional paid days off
Life insurance
Private pension plan

Fulltime

Physician Director Oncology Data Science - Translational Science

Are you looking for an opportunity to lead a Translational Data Science team wit...

Location

United States , Collegeville, Pennsylvania

Salary:

Not provided

GSK

Expiration Date

Until further notice

Requirements

medical degree
Completion of a clinical residency program leading to board qualification or certification in internal medicine, pathology, pediatrics is required
10 years plus academic or industry experience in Computational Biology, Bioinformatics, or Translational/Clinical AI with focus on Oncology
5 years of leadership or matrix leadership experience in Computational Biology, Applied AI/ML, Cancer Biology or a related field

Job Responsibility

Lead and build a growing team of Translational Data Scientists to support and innovate the Oncology portfolio pipeline
Leverage your clinical training and experience to translate complex computational and molecular insights into clinically meaningful hypotheses, study designs, and biomarker strategies that directly inform patient care and oncology clinical development
Contribute scientific expertise and design to multiple drug discovery or development efforts across oncology
Act as a competent and recognized expert in developing and critiquing the scientific validity of research/development initiatives to drive the development and delivery of long-term scientific strategy in Oncology Genomics
Individually contribute with analyses and integration of complex cancer datasets. This includes analysis of histopathology imaging data, gene & protein expression (bulk + single cell + spatial), somatic mutations, copy number alterations, and structural variants
Apply statistical methods and AI/machine learning algorithms to identify patterns in data, predict drug response, and discover potential biomarkers. Critically evaluate results. Conduct survival analysis to assess the impact of various factors on patient outcomes
Lead the development and use of bioinformatics pipelines
Serve as a recognized leader in driving technological foresight within specific scientific function or directing content of programs
Lead and influence the outcome of multidisciplinary meetings including partners in therapeutic research units, translational and clinical development teams.
Communicate complex scientific findings clearly to both technical and non-technical audiences.

What we offer

Competitive base salary
Annual bonus based on company performance
Flexible working options available for most roles
Learning and career development
Access to healthcare & wellbeing programmes
Employee recognition programmes

Fulltime

Associate Director, Compliance Systems & Analytics

The Associate Director, Compliance Systems and Analytics, is primarily responsib...

Location

United States , San Mateo

Salary:

167000.00 - 195000.00 USD / Year

Dompé

Expiration Date

Until further notice

Requirements

Bachelor's or Master's degree in a related field (e.g., Data Science, Computer Science, Life Sciences)
8+ years of experience in U.S. healthcare compliance, with expertise in data operations, governance, and strategy
Extensive experience with laws, regulations, and industry guidance that affect the biotech, pharmaceutical, and rare disease space, including but not limited to OIG, PhRMA Code, healthcare standard operating procedures, ABAC laws, and transparency reporting
Demonstrated understanding of U.S. healthcare compliance data assets and data ecosystems
Strong analytical and technical skills
proficiency in common analytics and CRM tools such as Excel, BI tools (Looker, Tableau)
Hands-on experience with modern data science / AI analytics tools such as Python (pandas/conda/matplotlib), R (tidyverse, plotly) or SAS and their related ecosystems
Proven success in building cross-functional partnerships and translating data into thoughtful, documented, risk-based decisions
Ability to effectively communicate complex data insights through compelling narratives to drive informed decision-making and foster a data-driven
Strong leadership, excellent communication, and stakeholder management skills

Job Responsibility

Embody Dompé’s commitment to ethics and integrity and values-based decision-making, and foster this mindset in clients, partners, and team members
Under the direction of the U.S. Compliance Officer, and will partner closely with the Legal, Information Communications Technology (ICT), Commercial Data Strategy and Operations, and Medical / R&D Teams
Design, implement, and manage a structured approach to analyze healthcare compliance-relevant data from various sources (e.g., investigations metrics, monitoring findings, transfers of value to healthcare professionals) to support a data-driven approach to U.S. healthcare compliance and risk management
Advise and create analytical requirements for dashboard creation, potential data requirements, and related business rules in order to bring necessary level of rigor
Ensure best practices for data reliability, ingestion, analysis, and output across various data streams
Develop strategy and support in enhancing key compliance systems, including but not limited to systems to review and approve key business activities (e.g., onboarding third parties, engaging healthcare professionals, reviewing external funding)
Assist in developing materials for Ethics & Compliance Committee meetings and other executive reporting, including external benchmarking, internal compliance metrics (e.g., dashboards), and compliance program vision
presents at such meetings where required
Evaluate and manage relationships with key systems, technology, and data vendors to maintain existing compliance systems and propose other cost-effective solutions
Identify and analyze regulatory landscape and external, industry trends regarding the use of technology and digital tools, including Artificial Intelligence (AI)

What we offer

Comprehensive medical benefits: we value access to healthcare for our patients as well as our employees
Generous vacation / holiday time off: we care about our employees and encourage a balanced lifestyle
Competitive 401(K) matching

Fulltime

Senior Director, Head of Argentina Clinical Data Sciences

As part of the Clinical Data Sciences (CDS) group, an integral delivery unit wit...

Location

Argentina , Buenos Aires

Salary:

Not provided

Pfizer

Expiration Date

Until further notice

Requirements

University or college degree in life science, computer science, pharmacy, nursing, or equivalent relevant degree. Advanced degree preferred
Ideally 20 or more years’ experience in drug development with at least 10 years in Clinical Data Management
At least 10 years' line management or global project team leadership experience
Clinical development and business experience in order to have a thorough understanding of regulatory processes at a global level
Recognition in peer community as expert and leader in topic area
Ability to leverage network to establish/maintain contact with scientific community
Exceptional technical and problem solving skills, and ability to evaluate computer systems for Data Management
Excellent understanding of clinical trials methodology, GCP and medical terminology
Experience of interaction with major regulatory authorities (not only in India)
Ability to work under pressure, demonstrating a high level of initiative and flexibility

Job Responsibility

Within CDS, lead a regional team comprised of multiple specialized functions and the local resources supporting and/or leading global trials across multiple TAs
Lead and influence across R&D on behalf of their TA Group or Function as a key component of cross-functional R&D planning
Build a brand-new and/or foster CDS departmental presence that has a strong local culture while being a fully integrated member of the worldwide CDS organization
Develop a departmental roadmap starting with the departmental vision, defined through targeted outcomes, strategic initiatives, and tactical deliverables
Ensure strong partnerships within global CDS, across R&D through collaborations with senior leaders (SVP, VP, ED and SD), senior level stakeholders and with external vendors
Act as a thought leader with the network to drive innovation within the organization and across the industry. Lead the conversation in key industry forums through presentations and publications
Lead clinical and non-clinical cross-functional special projects aimed to evolve CDS and partner functions in line with the Pfizer organization and the changing industry landscape
Set current and future strategy as a core member of the CDS Leadership Team
Span of control of 50 or more people or equivalent in terms of functional areas of accountability
As requested, deputize for the responsibilities of the Global Head of CDS

Fulltime

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Director, Data Science, Groups

Job Description

Job Responsibility

Requirements

Nice to have

What we offer

Looking for more opportunities?

Director, Data Science, Groups

Executive Director, Curio Science

Director Data Science

Director, Group Lead, Data Surveillance, Clinical Data Sciences

Senior Director, Data Science

Associate Director, Data Governance, Standards & Quality, RIM&DO

Physician Director Oncology Data Science - Translational Science

Associate Director, Compliance Systems & Analytics

Senior Director, Head of Argentina Clinical Data Sciences

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