Senior Specialist, Technical Project Management
MSDAbout the role
Job Description
We are looking for a Technical Project Manager to drive technical changes and work with appropriate internal and external stakeholders to help us deliver technical solutions with the highest value, that improves the way we run our clinical trials for our patients, our partners, and our employees.
Candidate will have a strong background in managing Technical Projects, are intellectually curious, eager to learn and execute and a self-starter.
As a Technical Project Manager, candidate will play a key role within the team working closely with PMO Leads, technical leads, software engineers, architecture team, product managers, vendors, other technical project managers, and business functional area members across the organization hierarchy both within and across organization.
Candidate will join our Project Management Office (PMO) for one of our Company’s Enterprise-wide Accelerate multiyear program, that focuses on technology and process transformation, simplification and innovation to:
Invest in data that fuel innovation
Modernize our current state clinical technology and business processes by implementing a new unified clinical platform
Transform the way we conduct our clinical trials.
Improve the clinical trial experience for our patients.
Improve efficiency, reduce cycle time and enable our business users to focus on what matters.
Responsibilities:
Work closely with cross-functional teams to ensure technical capabilities and Business deliverables are documented, executed and released on time.
Own, drive and provide oversight for the implementation of programs and projects within program, while being able to influence to gain alignment with stakeholders through use of data and logic.
Support creation and management of all aspects of a given project, accountable to gather information, create and maintain deliverables in Jira project with clear dependencies for accurate reporting, support business case creation, and implementation.
Identify and manage dependencies of varying complexity, potentially planning and feeding into overall program.
Communicate clearly with all stakeholders to remove obstacles and tackle challenges that arise in complex technology projects.
Create and maintain PMO Risk, Issue, Decision logs, Jira advance roadmap and confluence.
Tracks activities against the project schedule, managing stakeholder involvement as appropriate. Monitor costs, times, quality and resources used, take action where these exceed agreed tolerances.
Gain understanding of the problems or issues, manage resolutions, document impact, lessons learned, and clearly articulate those to stakeholders.
Maintain MS Project plan with relationship diagram and create timelines slides with dependency for reporting.
Schedule and facilitate project meetings, ensuring agendas are set and pre-work for workshops is prepared and effectively lead discussions to ensure groups don’t lose focus on real priorities.
Required Experience and Skills:
Bachelor’s degree in computer science, data science, life science, business administration, or related fields.
3+ years in Project and/or Program Management supporting Information Technology, or Pharmaceutical Research or Clinical Trial Operations or Business Management
3+ Experience working with agile methodologies and managing agile teams (scrum, kanban, etc.).
Hands on experience with Jira, Confluence, MS Office Suite, MS Project, and other project planning & Reporting tools.
Strong written and verbal communication skills, storytelling skills – listening with empathy, able to influence and effectively communicate complex concepts in simple ways for technical and business audiences.
Experience working within a team supporting regulated applications deployments and change control processes (GxP, SDLC).
A genuine interest in learning and development, self-motivated, embraces innovative ideas and fosters a collaborative atmosphere in a global organization.
Proficiency in written and spoken English.
Preferred Experience and Skills:
PMP or equivalent or Scrum Master or Product Owner certification
Prior experience in the pharmaceutical industry or Clinical Trial Operations or Information Technology.
Basic understanding of the Clinical Trials domain from the data collection and management perspective.
Project management experience working with stakeholders developing, testing and deploying GxP application, System Development Lifecycle (SD
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