Pharma Project Leader: Drug Development (Hybrid)

Placements24

Johannesburg

Hybrid

ZAR 1,200,000 - 1,800,000

Full time

4 days ago
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Benefits offered by this job

Competitive salary
Performance-based bonus
Medical insurance
PTO and holidays

Job summary

Placements24 is seeking a Senior Project Manager to lead complex drug development programs in Johannesburg. The role combines strategic planning, cross-functional leadership, and regulatory knowledge to drive projects from early research through clinical trials and submission.

You will define scope, timelines, budgets, and resource needs, mentor junior managers, and ensure compliance with GCP/GMP. The position offers a hybrid work model, competitive compensation, and opportunities for

Qualifications

  • 8+ years of progressive pharma project management experience.
  • Experience leading drug development through clinical phases.
  • Knowledge of GMP/GCP and regulatory affairs.
  • PM certification (PMP) desirable.

Responsibilities

  • Lead multiple pharmaceutical development projects from inception to completion.
  • Develop project plans with timelines, budgets and resources.
  • Coordinate cross-functional project teams and meetings.
  • Monitor progress, risks, and mitigations.
  • Manage budgets and ensure financial constraints.
  • Liaise with external partners and stakeholders.
  • Prepare status reports for senior management.
  • Ensure adherence to regulatory standards (GCP, GMP).
  • Drive process improvements in PM practices.
  • Mentor junior project managers and team members.

Skills

Project management
Leadership
Negotiation
Communication
MS Project
Jira
Agile
Waterfall
Stakeholder management

Education

Bachelor's degree in a scientific or technical field
MBA or MSc/PhD preferred

Tools

MS Project
Jira

Job description

Placements24 is seeking a Senior Project Manager to lead complex drug development programs in Johannesburg. The role combines strategic planning, cross-functional leadership, and regulatory knowledge to drive projects from early research through clinical trials and submission.

You will define scope, timelines, budgets, and resource needs, mentor junior managers, and ensure compliance with GCP/GMP. The position offers a hybrid work model, competitive compensation, and opportunities for

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