R&D Project Manager​/Scientific Project Manager

Position Summary

Radio Medix is seeking a highly organized, scientifically strong R&D Project Manager with a PhD in biology, chemistry, radiochemistry, pharmaceutical sciences, or a related discipline to support and advance a growing portfolio of radiopharmaceutical research and development programs.

This individual will serve as the operational backbone for RMX R&D projects—driving timelines, coordinating cross‑functional activities, identifying risks, maintaining clear documentation, and ensuring that project decisions are translated into actionable next steps. Unlike a traditional project manager, this role requires someone who can understand the science, review data at a high level, participate in technical discussions, and provide hands‑on support to laboratory activities when needed.

The ideal candidate is comfortable moving between the lab bench, project plans, data review meetings, and cross‑functional leadership discussions. They will bring structure and accountability to complex scientific programs without creating unnecessary bureaucracy.

• Lead day‑to‑day planning, coordination, tracking, and execution of RMX R&D programs, including preclinical, CMC, radiochemistry, analytical, and translational research activities.
• Develop and maintain integrated project plans, timelines, work streams, milestones, deliverables, dependencies, and critical paths.
• Facilitate recurring project team meetings, prepare agendas, document decisions, track action items, and ensure follow‑through.
• Identify program risks, resource constraints, technical dependencies, and timeline threats early; develop mitigation plans with project leads.
• Coordinate activities across R&D, radiochemistry, analytical development, QC, QA, manufacturing, regulatory, clinical operations, and external collaborators.
• Prepare concise project dashboards, status updates, decision logs, meeting minutes, and leadership presentations.
• Help prioritize R&D activities based on program objectives, development stage, available resources, regulatory needs, and strategic value.
• Maintain clear ownership across work streams and ensure deliverables are completed on time and to the expected scientific standard.

• Participate actively in scientific discussions and demonstrate the ability to understand experimental design, study objectives, data interpretation, and technical risks.
• Review experimental data, reports, protocols, and presentations for completeness, consistency, scientific rationale, and alignment with program goals.
• Assist with planning and coordinating in vitro, in vivo, radiochemistry, analytical, formulation, and stability studies, as applicable.
• Support preparation, review, and organization of study protocols, technical reports, development summaries, and supporting documentation for regulatory submissions.
• Serve as an additional technical resource for the R&D team by helping organize experiments, compile data packages, prepare figures, draft summaries, and follow up on study outcomes.
• Provide hands‑on laboratory support when needed, including assisting with study preparation, sample organization, documentation, inventory coordination, and other appropriate bench activities.
• Help ensure data generated across projects are organized, traceable, review‑ready, and available for internal decision‑making, partner discussions, and regulatory use.

• Work closely with laboratory personnel to improve planning, scheduling, documentation, material readiness, and communication across experiments.
• Assist with laboratory organization, reagent and consumable tracking, equipment scheduling, and coordination of external testing or study vendors.
  
  Help establish practical R&D operating rhythms, including project templates, experiment tracking tools, data review processes, and standardized meeting structures.
• Support the transfer of R&D knowledge and data packages to CMC, manufacturing, quality, regulatory, and clinical teams as programs mature.
• Contribute to continuous improvement of R&D workflows, documentation practices, and cross‑functional communication.