Remote Senior Project Manager — Drug Development Leader

Placements24

Johannesburg

Hybrid

ZAR 900,000 - 1,700,000

Full time

10 days ago

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Benefits offered by this job

Competitive salary
Performance-based bonuses
Health and wellness benefits
Retirement savings plan
Career advancement opportunities

Job summary

Placements24 seeks a Senior Project Manager to lead drug development programs in a fully remote setting. You will oversee all stages from discovery to regulatory submission, ensuring timely delivery within budget and high quality.

The role requires senior leadership and strong cross-functional collaboration across global teams. The ideal candidate has 7+ years in pharmaceutical project management, deep lifecycle knowledge, and experience navigating FDA/EMA guidance.

Qualifications

  • 7+ years in pharmaceutical project management, with drug development focus.
  • Strong knowledge of development lifecycle and regulatory requirements.
  • Proven track record in complex drug development projects from concept to submission.

Responsibilities

  • Lead cross-functional project teams through all phases of drug development.
  • Develop detailed project plans with timelines, milestones, and budgets.
  • Identify risks, implement mitigation strategies, and manage issues.
  • Ensure effective communication among teams, stakeholders, and partners.

Skills

Project leadership
Communication
Regulatory understanding
Remote collaboration
Agile
Waterfall
PMP (desirable)

Education

Master's degree in a scientific discipline
PhD in related field
MBA (plus)

Tools

MS Project
Smartsheet

Job description

Placements24 seeks a Senior Project Manager to lead drug development programs in a fully remote setting. You will oversee all stages from discovery to regulatory submission, ensuring timely delivery within budget and high quality.

The role requires senior leadership and strong cross-functional collaboration across global teams. The ideal candidate has 7+ years in pharmaceutical project management, deep lifecycle knowledge, and experience navigating FDA/EMA guidance.

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