Specialist, Technical Product Management

The Opportunity

Join a global healthcare biopharma company and be part of a 130+ year legacy of success backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.

Be part of an organisation driven by digital technology and data-backed approaches that support a diversified portfolio of prescription medicines, vaccines, and animal health products.

Drive innovation and execution excellence. Be a part of a team with passion for using data, analytics, and insights to drive decision-making, and which creates custom software, allowing us to tackle some of the world's greatest health threats.

Our organization partners closely with our Company’s Research & Development (R&D) organization to provide innovative solutions that enable new products and capabilities within the Research & Development. We collaborate internationally to deliver the services and solutions that help everyone to be more productive and enable innovation.

To enable this, we are seeking an experienced Associate Director, Technical Product Management supporting the Clinical Data Management ecosystem to join our team. The product manager will partner with R&D and other organizations to define the roadmap, own and prioritize the backlog and be the central contact between the business and scum team.

Responsibilities

• As a Product Analyst within the Integrated Trial Monitoring Product, you will work across our area supporting programs which enable our business partners to operate without obstacles.
• You will build expertise on system validations and will have the opportunity to learn the end-to-end clinical process.
• You will work with stakeholders at all levels across our company to uncover and communicate user needs.
• You will be instrumental in planning, designing, and conducting testing activities, engaging support teams, and compiling critical content for training and communication to users.
• You will apply a structured approach to discover, document, and manage business process and stakeholder needs.
• You will also gather insight into user journey, behaviour, motivation, unarticulated problems, unmet needs and pain points.
• You will work side by side with Business Stakeholders, Product Users, Product Managers, and Technical Leads and you will be providing close support to ensure that the IT solutions are both valuable and viable.
• Additionally, You Will
• Gather documentation related to the business process in clinical domain, document business/user needs and trace requests and responses to requests
• Continuously broaden your expertise in the Clinical Trials business domain
• Leverage business and user insights to form solutioning ideas and make prioritization decisions to maximize the value of the IT solutions Work with the business to identify business value for our initiatives and determine the best way to measure that our solutions achieve the targeted business value
• Be accountable for enablement, adoption, and growth of the Integrated Trial Monitoring product
• Build knowledge of the existing solutions through IT communities and leverage these for the benefit the business stakeholders
• Partner with squad members including but not limited to scrum masters, technical lead(s) and development team to manage high-quality product delivery leveraging Agile SDLC methodology
• Work closely with stakeholders to ensure a healthy backlog of well-formed epics, features and user stories are maintained, which align with the overall roadmap and serve as requirements for the delivery squad
• Follow and apply the Product Model principles to maximize the business value
• Education
• Minimum
• H.S. Diploma
• Preferred
• Bachelors#MSJR

Required Skills

• Animal Vaccination, Asset Management, Benefits Management, Biopharmaceutical Industry, Business Documentation, Business Management, Business Processes, Business Process Management (BPM), Business

Requirements

• Documentation (BRD), Decision Making, Foster Innovation, Global Health, Management System Development, Medical Prescriptions, Product Lifecycle, Product Management,

Requirements

• Management, Stakeholder Relationship Management, Strategic Planning, System Designs

Preferred Skills

• Current Employees apply HERECurrent Contingent Workers apply HEREUS 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.

Requirements

• 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 RightsEEOC 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 ActsThe salary range for this role is$87,300.00 - $137,400.00This 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 https://jobs.merck.com/us/en/compensation-and-benefits.

You can apply for this role through https://jobs.merck.com/us/en (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 OrdinanceLos 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 OrdinanceSearch 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 StatusRegularRelocation:

No relocationVISA SponsorshipNoTravel

Requirements

• No Travel

Required

• Flexible Work Arrangements
• Hybrid
• Shift
• Not Indicated
• Valid Driving License
• NoHazardous Material(s)
• N/AJob Posting End Date07/18/2026A 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:R407969