Associate Director, R&D Program Management Job at BD (Covington)

Global Category Associate Director- Data Analytics and AI Platforms

We are seeking an individual who thrives in ambiguity, capable of driving catego...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Familiarity with procurement platforms such as Ariba, as well as ERP systems and advanced analytics tools to support decision-making and process automation
Excellent problem solving and organizational skills
Experience leading large, cross-functional teams and managing complex global projects in a matrixed environment
Experience managing analytics and AI/ML software procurement
Understanding of cloud data ecosystems (e.g., Snowflake, Databricks, AWS/Azure/Google AI)
Strong analytical skills with ability to assess large data sets and supplier performance
Doctorate degree and 14 years of Global Strategic Sourcing, Procurement or Commercial experience OR Master’s degree and 15 to 17 years & above experience of Global Strategic Sourcing, Procurement or Commercial experience OR Bachelor’s degree and 17-18 years of Global Strategic Sourcing, Procurement or Commercial experience
And 2 years of managerial experience directly managing people and/or leading teams, projects, or programs.

Job Responsibility

Lead and evolve the category strategy for Data Analytics and AI Platforms, enabling Amgen to leverage data-driven insights across R&D, Commercial, Operations and G&A functions
Partner with Digital, Data Science, and IT leaders to standardize platforms such as data lakes, analytics, and AI/ML environments
Evaluate emerging suppliers in data, AI, and predictive analytics to incorporate innovation responsibly
Design contracts balancing access to innovation with compliance, governance, and cost efficiency
Develop multi-year sourcing roadmaps to ensure data and AI platforms meet enterprise growth and compliance needs
Provide strategic oversight as the global lead for Software category and sourcing, ensuring alignment between category strategies and Amgen’s evolving business needs
Act as a trusted advisor to ensure that procurement initiatives are aligned with broader organizational objectives
Guide and facilitate collaboration across cross-functional teams and regional stakeholders
Ensure that all Software procurement activities are managed in compliance with regulatory, contractual, and operational risk requirements
Partner with Legal, Compliance, Data Privacy, and Cybersecurity teams to maintain oversight of risk mitigation strategies

Director, Department of Programs

The Director, Department of Programs (DoP) ensures Geneva’s research and develop...

Location

United States , Bethesda; San Antonio

Salary:

160000.00 - 180000.00 USD / Year

THE GENEVA FOUNDATION

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Business Administration, Management, Public Health, or related field required
advanced degree (MBA, MHA, MPH, or equivalent) strongly preferred
12+ years of progressive leadership experience in research administration, research operations, or related non-profit, academic, or government environments
Experience leading R&D business development in a DoD, industry, or higher education environment
Proven track record building pre-award capacity that actively drives proposals including capture planning, non-technical volume ownership, lay reviews, and submission readiness
Expertise in federal and non-federal sponsor regulations, contracts, and grants management
Demonstrated success in building and scaling high-performing teams with clear accountability and measurable results
Demonstrated financial acumen in profitability management of federally funded research and industry-sponsored clinical trials
Proven record of shaping and executing growth strategies that expand research funding, strengthen R&D pipelines, and build institutional partnerships
Strong operational acumen, with experience in compliance oversight, risk management, and QA/QC system implementation

Job Responsibility

Lead annual goal setting, performance monitoring, and reporting for DoP
Actively serve on the Department Leadership Team to ensure Geneva’s vision is translated into actionable strategies and measurable outcomes
Ensure compliance with federal, non-federal, and Geneva regulations, including human subjects’ protection, animal welfare, intellectual property, conflict of interest, and cost-accounting standards
Advance modernization of enterprise systems, data, and QA/QC processes to strengthen efficiency, transparency, and decision-making
Benchmark Geneva’s practices against leading institutions to adopt and execute best-in-class standards
Conduct risk analyses and develop mitigation strategies to reduce organizational vulnerabilities
Oversee departmental budget development, monitoring, and variance management to ensure responsible growth and resource optimization
Deliver accurate and timely reporting of meaningful metrics to demonstrate performance, customer satisfaction, and strategic impact
Manage long-term planning for research operations, aligning people, infrastructure, and technology with growth projections
Work with Finance to articulate audit readiness and ensure audit-ready records within DoP

What we offer

medical, dental, and vision healthcare
Flexible Spending Account
Health Savings account, with employer contribution
Coverage is provided for employees and family members including domestic partners
Short-and long-term disability
Employee Assistance Program
Life & ADD insurance
403b retirement plan with generous employer match
flexible leave options
11 paid holidays per year

Fulltime

Associate Director, Alliance Management Operations

We are seeking a creative, self-starting, and entrepreneurial Associate Director...

Location

United States , Waltham

Salary:

160000.00 - 200000.00 USD / Year

Kailera Therapeutics

Expiration Date

Until further notice

Requirements

3+ years of experience in alliance management or partnership operations, business development operations, R&D or Commercial operations, or top-tier consulting within the USA biopharma or biotech industry
8+ years of overall progressive experience in the life sciences industry or other relevant experience
A creative operations leader who has a sharp sense for data collection, tracking, and reporting. Excels at story telling using information, personal knowledge, and data. Ability to create dashboards and reports for functional and executive leadership
The ability to work independently and successfully in a matrix environment, prioritize and manage multiple projects and tasks simultaneously, and thrive in a dynamic environment
Demonstrated expertise having integrated organizational or cross-functional information into systems and tools to input, track, manage, report, and optimize the operations of a program, department, or company
Expert-level proficiency in analytical skills, information technology, and project management, as well as in Microsoft Powerpoint and Sharepoint
Demonstrated quality of experience leveraging AI to drive business operations
Knowledge of the drug development process, particularly late-stage development, to enable meaningful dialogue with internal stakeholders and external partners
Comfortability and understanding of contractual terminology related to legal, business development, and/or licensing
Highly motivated, entrepreneurial individual, with an ability and willingness to navigate between high-level alliance/program strategy and day-to-day execution within a team-oriented culture

Job Responsibility

Implement our Alliance Management Operations systems, playbooks, and reporting, while operationalizing department strategy
Collaborate effectively with Kailera functional leaders, Partner’s alliance management team, and SaaS vendor to collect, input, and optimize the information necessary to build and manage comprehensive alliance management dashboards for the functional leaders and executive leadership team
Inform the organization of enterprise risks, opportunities, and inflection points related to alliance management
Champion alliance management best practices across the organization to ensure an insight-driven way of working and decision making
Operationalizing alliance governance and working group meetings, including meeting scheduling, agenda, and slides preparation with the alliance partner, meeting minutes, and tracking actions, decisions, issues
Alliance management records management and other general alliance management operational tasks

What we offer

comprehensive health coverage
flexible time off
paid holidays
a year-end shutdown
monthly wellness stipend
generous 401(k) match
tuition reimbursement
commuter benefits
disability and life insurance
annual bonus opportunities

Fulltime

Associate Scientist II

This is where your work makes a difference. At Baxter, we believe every person—r...

Location

United States , Round Lake

Salary:

80000.00 - 120000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Bachelor’s degree or equivalent experience in a relevant scientific field (e.g., chemistry, pharmaceutical sciences) with at least 2+ years of proven experience
Experience working with analytical chemistry instruments such as HPLC, pH meters, UV spectroscopy, titrations, particle analysis, TOC, flame photometry, and sample extraction techniques
Proficiency in a regulated environment and strong technical problem-solving skills
Excellent oral and written communication skills, strong analytical abilities, and keen attention to detail
Experience with Electronic Lab Notebooks and pharmaceutical GMP laboratories is preferred
Experience with Empower software is advantageous
Ability to manage multiple tasks concurrently and efficiently
Strong laboratory/technical, writing, and computer skills
Ability to effectively coordinate and communicate complex information with managers and peers

Job Responsibility

Conduct critical chemical and physical analyses on finished product R&D stability samples, and support testing of raw materials and other R&D initiatives
Act as a study director for studies, independently evaluating results and determining their impact
Provide training and supervision to junior members within the laboratory
Review test data meticulously, perform documentation reviews in LIMS and other computerized systems
Apply sophisticated laboratory instrumentation and computer systems for data collection and recording
Participate in validations and transfers, ensuring compliance with regulatory standards
Perform detailed chemical assays
Complete all testing, including special project/protocol testing, in a timely manner
Maintain data integrity and ensure compliance with company SOPs, FDA regulations, and other quality standards
Collaborate with various departments to solve problems, boost efficiency, improve quality, and provide outstanding product support

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
Medical and dental coverage that start on day one
Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP)
401(k) Retirement Savings Plan (RSP)
Flexible Spending Accounts

Fulltime

Associate Scientist II

This is where your work makes a difference. At Baxter, we believe every person d...

Location

United States , Round Lake

Salary:

80000.00 - 120000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Bachelor’s degree or equivalent experience in a relevant scientific field (e.g., chemistry, pharmaceutical sciences) with at least 2+ years of proven experience
Experience working with analytical chemistry instruments such as HPLC, pH meters, UV spectroscopy, titrations, particle analysis, TOC, flame photometry, and sample extraction techniques
Proficiency in a regulated environment and strong technical problem-solving skills
Excellent oral and written communication skills, strong analytical abilities, and keen attention to detail
Experience with Electronic Lab Notebooks and pharmaceutical GMP laboratories is preferred
Experience with Empower software is advantageous
Ability to manage multiple tasks concurrently and efficiently
Strong laboratory/technical, writing, and computer skills
Ability to effectively coordinate and communicate complex information with managers and peers

Job Responsibility

Conduct critical chemical and physical analyses on finished product R&D stability samples, and support testing of raw materials and other R&D initiatives
Act as a study director for studies, independently evaluating results and determining their impact
Provide training and supervision to junior members within the laboratory
Review test data meticulously, perform documentation reviews in LIMS and other computerized systems
Apply sophisticated laboratory instrumentation and computer systems for data collection and recording
Participate in validations and transfers, ensuring compliance with regulatory standards
Perform detailed chemical assays
Complete all testing, including special project/protocol testing, in a timely manner
Maintain data integrity and ensure compliance with company SOPs, FDA regulations, and other quality standards
Collaborate with various departments to solve problems, boost efficiency, improve quality, and provide outstanding product support

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
Medical and dental coverage that start on day one
Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP)
401(k) Retirement Savings Plan (RSP)
Flexible Spending Accounts

Fulltime

Associate Director, Clinical Data Manager

Associate Director, Clinical Data Manager (Sponsor Dedicated). ICON plc is a wor...

Location

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Advanced degree in Data Science, Statistics, Bioinformatics, or a related field
Experience in all aspects of Data Management related clinical study planning and execution, and in executing the complete range of clinical study activities, from concept sheet through final study report and archiving
Proven experience as Clinical Data Manager in the pharmaceutical/biotechnology industry, equivalent to at least 10 years
Substantial project management experience
Strong leadership competencies and influencing skills
Effective oral and written communication skills
Proven team dynamic knowledge and skills and ability to foster partnerships across projects and multidisciplinary teams
Growing expertise in drug development, including some knowledge of interfaces and interdependencies of clinical development with other functions (e.g., nonclinical & pharmaceutical development, regulatory, commercial/marketing)
Successful completion of multiple studies from beginning to end providing a full scope of DM experience

Job Responsibility

Leading Data Management including centralized monitoring related activities within a complete clinical development program (Phase I-IV, Accountable and Project Leadership) for global or regional trials and/or programs with different complexity
Serving as the escalation point, work with CRO data managers, vendors, internal team members for resolution
Ensures and tracks data quality of clinical database/deliverables (incl. CRF and non-CRF data) and submission readiness of the clinical data management deliverables and data packages (e.g. CDISC)
Project management of all clinical data management related deliverables including operationalization by steering internal and external experts and specialist. Ensuring adherence to planned time, cost and quality
Execution of the clinical data collection strategy in accordance to Sponsor Standards
Accountable for oversight of CROs in the execution of Phase I – IV clinical trial(s)
Represents Data Management within the Global Trial Team and serves as the key Global Development Operations point of contact for the DM related tasks in a trial/project/program
Key contributor to the development of reports and communicating to relevant line management and Clinical Operations Teams
Drives, leads and manages the successful execution, oversight and approval of all DM related clinical trial documents and operational plans (e.g. Data Management Plan) of clinical trials using strong project management, leadership, and organizational skills
Ensures strong oversight, review and delivery of trial/project DM related CAPAs in order to meet corporate compliance standards and timelines

What we offer

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others

New

Executive Account Manager

The Executive Account Manager is responsible for managing the relationship of to...

Location

United States

Salary:

Not provided

Parking Network B.V.

Expiration Date

April 12, 2026

Requirements

Extensive knowledge of T2’s software products, services, and processes
Extensive knowledge of various operating systems, software products
Strong time management skills
Knowledge of the parking industry
Knowledge of T2’s products, hardware, and services
Ability to push self to constantly improve
Ability to maintain a positive attitude and enthusiasm
Ability to read, analyze, and interpret financial reports, business, professional, and technical documents
Ability to respond to common inquiries or complaints from customers and staff
Ability to write presentations, articles, routine reports, proposals, and correspondence

Job Responsibility

Manage the relationship of top tiered existing assigned T2 customer accounts
Add on sales
Provide important customer updates, new solutions being offered, and events
Responsible for the renewal activities associated with the customer
Maintains regular contact according to targeted frequency with assigned accounts
Plan and schedule strategic customer in person visits
Attend and participate in industry and company conferences
Provide content and present throughout company/industry conferences
Fulfills regularly scheduled checklist of items to be covered with clients such as current company initiatives
Follows up on sales leads and develops leads

Fulltime

Associate Director, Decision Analyst

The Associate Director, Decision Analyst, will be responsible for analyzing data...

Location

United States , San Rafael

Salary:

153700.00 - 211310.00 USD / Year

BioMarin Pharmaceutical

Expiration Date

Until further notice

Requirements

Bachelor's degree in a scientific or technical field (e.g., Biology, Chemistry, Engineering) or equivalent experience
7+ years of experience in strategy or portfolio management within pharmaceutical/biotech company, or equivalent experience in management consulting or other industry with strong discipline in decision analysis
Ability to perform and synthesize in-depth analyses of asset and portfolio information, integrating findings into insights and actionable recommendations
Demonstrated ability to work cross-functionally across research, clinical development, commercial, and manufacturing teams
Excellent communication, interpersonal, and presentation skills
Strong organizational and problem-solving skills
Ability to work independently and as part of a team
Advanced degree preferred (MS or MBA), with a strong understanding of drug development, R&D strategy, and decision analysis

Job Responsibility

Support efforts to improve decision quality in the organization by developing and continuously improving decision analysis methodologies and best practices
Facilitate workshops to incorporate uncertainties into asset and portfolio scenario analysis
Work with Asset Teams, Program Management Leads, and SMEs to determine planning confidence levels and develop risk-adjusted development timelines and scenarios
Enhance and facilitate processes to estimate pre-clinical and clinical probabilities of success
Collect inputs for portfolio models that integrate attrition rates, clinical probability of success, timeline uncertainties, and commercial forecast scenarios to inform decision-making
Support portfolio optimization processes during financial planning cycles
Build, maintain and execute portfolio analysis processes and tools to support strategic decision making
Structure and perform scenario analyses and simulations to model and value strategic alternatives and trade-offs with the aim of maximizing value at an asset and a portfolio level
Provide support to teams for decision framing and decision analysis by demonstrating established methodologies
Supports periodic end-to-end portfolio performance reviews and health checks

What we offer

discretionary annual bonus
discretionary stock-based long-term incentives
paid time off
company-sponsored medical, dental, vision, and life insurance plans

Fulltime

Associate Director, R&D Program Management

BD

Location:
United States , Covington

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
March 19, 2026

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