Landmark Bio translates groundbreaking research into life-changing medicines. We provide development, manufacturing, and regulatory capabilities to help early-stage life science innovators rapidly progress advanced therapies from bench to clinic. Launched in 2021, and based in Watertown, Mass. Landmark Bio is an unprecedented venture bringing together the best of industry, academia and research hospitals to accelerate life sciences innovation. A public benefit company, our work advances emerging technologies, demonstrates therapeutic potential, and improves human health.
We are seeking a highly motivated and team-oriented professional with entrepreneurial spirit to join our company! This is an exciting opportunity for a well-qualified candidate to join a rapidly growing company focused on turning today’s cutting-edge research into tomorrow’s breakthrough therapies.
Scope of Responsibilities
•Serve as a Smartsheet Super User for the site, creating, managing, and optimizing complex workflow within the platform. Train and support others as needed.
•Develop and maintain tools for Landmark Bio including document and presentation templates, dashboards, trackers, etc. and recommend process improvements to existing tools and ways of working.
•Help with training of Landmark Bio personnel on evolving program management tools, including training documents/slide decks, office hours and demos, and one-on-one support.
•Collaborate with the PMO team members on new tool evaluations and training initiatives.
•Maintain internal program Teams sites and external client SharePoint sites to ensure documents are organized and easy to locate, archive documentation at the closure of programs.
•Write applicable program documents including charters, program plans, program schedules, RACI matrices, risk registers, business requirements, policies and procedures, and training materials. Ensure all program documents are complete, accurate, current, and stored appropriately.
•With the support of senior program managers: develop, execute, and oversee the coordination of program timelines, risk registers, and dashboards for internal and client facing programs.
•Generate documentation for changes in scope to be issued to the client.
•Assist with client meetings/teleconferences/onsite visits, ensuring minutes and actions are taken and all required program documentation is generated by self or the project team.
•Assist with sharing lessons learned across programs to improve collective efficiency.
•Coordinate program materials and the use of shared resources; escalate resource constraints when identified.
•Create and update presentations in preparation for team and leadership reviews.
Qualifications
•BS degree with 5+ years relevant experience (GMP pharmaceutical, biologics, and/or cell and gene therapy field) is required
•PMP certification desired
•High degree of proficiency in Smartsheet is required, including advanced skills in workflow design and implementation, template creation and management, user training and support, and reporting and analytics
•Strong communication, problem solving, planning, and project management skills
•Ability to support more than one project of a reasonable size simultaneously
Landmark Bio is an Equal Opportunity, Affirmative Action employer. Minorities, women, veterans, and individuals with disabilities are encouraged to apply.
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