Assoc. Dir , Product Manager, Disease Biology & PharmTox
- Partner closely with R&D scientists and Business Technology Partners to own, set, and communicate the product vision, strategy, and outcome roadmap, aligned with strategic priorities -
- Deeply understand user needs (scientists, data scientists, lab operations) through interviews, shadowing, and usage analytics- -
- Map processes and information architecture to identify pain points and automation opportunities -
- Define clear problem statements, requirements, and success metrics and utilize these artifacts author Product Requirements Document -
- Drive solution discovery and rapid prototyping with cross-functional teams to evaluate value, usability, feasibility, and business viability -
- Prioritize features and trade-offs using impact, effort, and risk frameworks; manage backlog and release planning -
- Manage scientific applications and lead squads to build user-friendly scientific data and technology products; handle risk assessment and vendor engagement as needed -
- Evaluate internal and external tools; Manage vendor relationships to influence roadmaps and integrate with internal systems and the data lake -
- Partner with Product Tech leads/Engineering leads to ensure seamless integration across the ecosystem and upstream/downstream systems -
- Apply industry standards and ontologies to develop FAIR (Findable, Accessible, Interoperable, Reusable) applications, advancing in silico models and AI/ML approaches for drug discovery -
- Create and maintain documentation including SDLC deliverables (GxP and non-GxP), guidelines, SOPs, training materials, and user communications -
- Support regulatory audits and inspections by collaborating with stakeholders and Quality-to provide documentation and respond to inquiries -
- Coach teams to adopt a customer-centered product mindset; proactively remove roadblocks and escalate issues to maintain momentum -
- Drive adoption using metrics and user feedback; analyze engagement, create reports/visualizations, and run user groups to inform continuous improvement -
- Promote available capabilities to stakeholders, fostering collaboration and integration across teams to avoid silos -
- Develop a cohesive strategy to manage an orthogonal suite of products and applications, maximizing impact while reducing costs and redundancy -
- Diligently manage total cost of ownership -
- Monitor the competitive landscape, standards, and emerging technologies in scientific software and data platforms -
- Use data-driven insights (synthesized from research, observations, and usage) to inform decisions and refine strategy -
- 5+ years of experience in scientific software development, pharmaceutical sciences, target discovery, or scientific data management -
- Strong understanding of preclinical development domain and processes -
- Proven experience leading-multidisciplinary squads-to launch and manage software products; translate business needs into user stories and product requirements -
- Experience with scientific workflows (COTS, in-house, open source); ability to assess, integrate, and scale them -
- Solid grasp of SDLC and Agile practices; comfortable operating in GxP-regulated environments -
- Exceptional communicator who bridges science, engineering, and business; customer-centric and effective in a matrixed organization -
- Proficient with product and UX tooling (e.g., Jira, Confluence, Mural, Figma, Balsamiq); capable of producing clear documentation and visuals -
- Working knowledge of data models, ontologies, and information architecture in drug discovery -
- Proven ability to work independently and asynchronously across time zones, with excellent cross-cultural and organizational communication skills
- Highly organized, with strong project and stakeholder management capabilities
- Demonstrated ability to operate at both strategic and execution levels, balancing long-term product vision with near-term delivery
- M.A./M.S. with 3+ years, or B.A./B.S. with 5+ years of experience in a scientific or technical discipline such as biology, pharmaceutical sciences, bioinformatics, computer science, biostatistics, biomedical engineering, or chemistry
- Experience as a scientist, Informatics Analyst or IT analyst in a drug discovery or development environment, specifically pre-clinical development area
- Experience using AI-powered product tools (e.g., for backlog refinement, requirements generation, user insights synthesis, prototyping)
- Familiarity with integrating AI-enabled tools into scientific workflows (e.g., data annotation, AI driven data entry)
- Ability to define and measure value for AI-driven features (e.g., accuracy, explainability, user trust, adoption)
- Experience supervising and mentoring team members
- Proficiency with data analytics/mining tools (e.g., R, Python)
- Familiarity with structured, relational databases and data integration.
- Skill in data visualization and dashboards with the ability to craft compelling data narratives (e.g. PowerBI)
- Experience working in Agile development environments
Asset Management, Benefits Management, Business Translations, Client-Centric, Data Insights, Data Science, Drug Discovery Process, Emerging Technologies, Information Architectures, Job Descriptions, Management System Development, Product Management, Requirements Management, Scientific Data Management, Scientific Software, Scientific Software Development, Stakeholder Relationship Management, Strategic Planning, System Designs, Vendor Management Preferred Skills: Current Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only: Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.--As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.- For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement• We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts The salary range for this role is
$142,400.00 - $224,100.00 This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee's position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable. We offer a comprehensive package of benefits.- Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at . You can apply for this role through (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting. San Francisco Residents Only: -We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los Angeles Residents Only: -We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance Search Firm Representatives Please Read Carefully-
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. -No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.- Employee Status:
Regular Relocation:
No relocation VISA Sponsorship:
No Travel Requirements:
25% Flexible Work Arrangements:
Not Applicable Shift:
Not Indicated Valid Driving License:
No Hazardous Material(s):
n/a Job Posting End Date:
07/24/2026
*A job posting is effective until 11:59:59PM on the day BEFORE -the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Requisition ID: R406577
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