Director of Planning and Project Management Job at Bolt Medical, Carlsbad, CA

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  • Bolt Medical
  • Carlsbad, CA

Job Description

DIRECT CANDIDATES ONLY, IF INTERESTED APPLY THROUGH JOB POST. NO DIRECT MESSAGES.

RECRUITERS: DO NOT CONTACT.

Responsibilities:

Overall:

  • As a Project Management Leader, you lead/manage all cross functional project teams to plan, execute and achieve company objectives from concept through commercial launch.
  • This role puts strong emphasis on agility, strategic thinking, complex problem-solving and ability to influence others to drive results and may include supervision of direct reports upon hire or future opportunities for role expansion
  • Develop and manage project plans to identify and complete milestones with accountability for successful completion of all project deliverables
  • Serve as the primary lead project manager for multiple devices and a console
  • Provide direction, guidance, and oversight to core teams to execute projects for multiple clinical studies and initiatives on schedule and within budget
  • Determine resources, track forecasts, and set priorities for projects
  • Manage project status and ensure escalation and appropriate communication internally to key senior leadership/stakeholders
  • Facilitate/Lead cross functional teams to anticipate and communicate risks and lead in the implementation of mitigation strategies throughout design, verification testing, and clinical trials
  • Provide mentoring and coaching to other project team members
  • Actively leads multiple Project Management Office (PMO) continuous improvement activities

Planning:

  • Develop detailed project plans to meet clinical and regulatory objectives based on cross-functional input and analysis
  • Collaborate and influence to gain core team buy-in and team ownership of the plannal input and analysis
  • Manage the cross-functional integrated project plan and drive the execution through cross-functional teams, building the global project timelines, ensuring milestones, goals, risk and budget are achieved
  • Determines and discerns requirements on larger scale projects to establish the project deliverables and manages changes to the project scope and schedule

Team Leadership:

  • Lead cross-functional core team meetings
  • Build the following within the team: meeting discipline (agenda, minutes, action items), problem solving culture and accountability
  • Partner with project leads, cross-functional groups, and functional managers to define/manage resource requirements to support project objectives
  • Identify forward looking risk and determine mitigation plans with core team

Communication and Reporting:

  • Maintain weekly status reports, including timelines and performance dashboards
  • Maintain efficient and effective communication, per communication plan development and execution, to provide clarity for roles and responsibilities and alignment with stakeholders
  • Serve as conduit between project/team members in all cross-functional groups (e.g. Clinical, Ops, Quality, R&D, Regulatory, etc.)

Qualifications:

Education & Experience:

  • Bachelor’s degree with a minimum of 10 years of previous related experience including medical device, pharmaceutical, and/or biotech. Master’s degree or equivalent with 9 years of previous related experience as listed above
  • Experience managing large cross-functional projects related to the development of medical devices involving both disposable devices and a console (system)
  • Experience leading cross-functional team meetings, management updates and internal development review meetings
  • Experience managing the development of medical devices through initial launch within the US and EU or a combination thereof. Working knowledge of Design Control requirements (US, EU)
  • Medical device development experience with Class II or III interventional cardiology catheters such as IVUS, OCT, cardiac ablation/diagnostic, PTA/PTCA catheters, stent delivery systems and robotically driven catheters and their associated consoles
  • Knowledge of clinical studies
  • Working within in a start-up environment (early or late stage)
  • Critical Chain Project Management Experience using the Pro Chain suite of software (Scheduler, Enterprise and Pipeline)
  • PMP Certification

Skills & Abilities:

  • Strong problem-solving and analytical skills.
  • Excellent communication skills, capable of explaining complex technical concepts in clear, simple terms.
  • A collaborative team player.
  • Self-driven, highly motivated, with a passion for learning new technologies.

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