Global Project Director

5 days ago


Copenhagen, Copenhagen, Denmark Lundbeck AS, H Full time

Transform Lives with Innovative Development

We are seeking a highly motivated and experienced Global Project Director to join our dedicated cross-functional team. As a key member, you will work closely with the Global Project Lead to ensure successful pipeline progression of our innovative development projects.

Your Role:

  1. Develop global project plans and scenarios in collaboration with the cross-functional team.
  2. Ensure timely presentation content and readiness for governance endorsement meetings, project reviews, and information meetings.
  3. Participate in GPT meetings, ensuring goals and deliverables are defined and met.
  4. Oversee project budgets, identifying financial risks and collaborating with finance.
  5. Maintain oversight on project timelines, action points, critical issues, and deadlines.
  6. Report on project high-level information, including monthly status progression.
  7. Document and transparently communicate plans, actions, and decisions to the team.

About Your Future Team:

You will join a team of 18 highly motivated colleagues who take pride in creating value by serving people living with brain disease through strategic, operational, and transparent leadership of our projects and portfolio. We work on creative, high-profile projects advancing brain health and transforming lives. Our department culture is characterized by openness, dedication, and respect.

This role is based at our headquarters in Valby, Copenhagen, and is a 12-month maternity cover.

The Ideal Candidate:

  1. 3+ years of project management experience working with various stakeholders to deliver cross-functional activities.
  2. Pragmatic and progressive mindset with extensive cross-cultural/functional collaboration skills.
  3. Academic degree in science or similar and 5+ years of experience from a large R&D organization within the pharmaceutical industry/drug development.
  4. Thorough experience working within clinical development, research, regulatory, or CMC areas.
  5. Familiarity with the R&D value chain.


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