Project Manager with a strong scientific background managing pre-clinical programs for small molecule drug discovery and development. Join a fast-paced, early-stage biotech impacting patients in renal disease.
Responsibilities
Lead project team meetings – draft agendas, document key discussion points, actions, and decisions, and maintain program records for easy access by the team.
Ensure projects are conducted in compliance with industry regulations and organizational quality standards.
Drive development of program Gantt charts and summarize the critical path in timeline slides for team discussions and leadership meetings.
Proactively identify risks and potential roadblocks in the project pipeline and develop mitigation and contingency strategies. Communicate plans to senior management and stakeholders.
Coordinate across various internal functions, including medicinal chemistry and biology teams to drive projects forward, ensure all stakeholders understand their deliverables, and prioritize key workstreams.
Ensure projects proceed according to agreed timelines and budget, flagging for stakeholders and leadership when a timeline or budget deviation is anticipated.
Identify resource gaps for projects and highlight the impact to timelines/budget for stakeholders and senior management.
Perform scenario planning to facilitate team decision making and prepare for multiple potential outcomes.
Partner with scientific leads and legal team to negotiate and establish contracts with CROs, academic partners, and consultants.
Provide operational support to program teams, including international and domestic shipping, PO generation, and managing SharePoint folder structure.
Continuously seek ways to improve our workflows, internal project management processes, and tools.
Requirements
Bachelor’s degree in Life Sciences, Pharmaceutical Sciences, Chemistry, or a related field (Master’s degree or PhD preferred).
PMP certification or equivalent project management training is a plus.
2+ years of experience in project management in the biotech, pharmaceutical, or related industry, with a focus on pre-clinical or small molecule drug development.
Experience working in drug discovery and pre-clinical development stages (e.g., early-stage drug discovery, animal studies, ADME/Tox).
Strong understanding of small molecule drug development processes, including pharmacokinetics, toxicity studies, formulation, and scale-up.
Proven ability to manage cross-functional teams, multiple vendors and projects simultaneously.
Exceptional organizational and time management skills, with an ability to manage competing priorities and deadlines.
Excellent written and verbal communication skills, with the ability to present complex information in a clear and concise manner.
Solid problem-solving and critical thinking skills, with the ability to anticipate challenges and address them proactively.
Proficiency with project management software, such as Smartsheet.
Familiarity with pre-clinical data analysis and reporting tools is a plus.
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