Seuss +

Project Director

5 days left

Seuss +
22 Sep 2021
22 Oct 2021
Clinical Research
Full Time
Contract Type
Experience Level
Experienced (non-manager)
This is an exciting opportunity to work for a scientific and open-minded CRO headquartered in the Netherlands.

Are you looking for an organization that encourages ideas, out of the box thinking and offers a safe place to grow?

We're searching for an experienced and entrepreneurial (Associate) Project Director on behalf of our client.

Your New Role

Are you looking for the next step in your career? If you are an experienced Project Director or have senior clinical project management experience with a broad background in managing clinical trials, this could be the perfect match.

As (Associate) Project Director, you will be responsible for overseeing (international) industry-driven, high-profile studies in CNS and other indications Infectious Diseases. Reporting directly to the Head of Project Management.


This is a dynamic and diverse role where you'll be the bridge between academic research and trials for biopharmaceutical companies while securing new business and overseeing the delivery of projects.
  • Provide direct supervision, support, training and mentoring to a staff of Project Managers.
  • Line management responsibility for a team of project managers.
  • Be an active member in the Therapeutic Expert Teams, which bring together operations, science and business development.
  • Find creative solutions to the challenges that many clinical trials pose.
Do you enjoy?
  • Providing strategic direction, leadership and management across multiple divisions to direct the delivery of projects/programs within cost, time and quality requirements?
  • Providing direct supervision, support, training and mentoring to a staff of Project Managers?
Your Experience
  • Academic level of education in biomedical sciences.
  • A minimum of 10 years of progressive experience in life sciences, including 5 years of experience in a project management position in the biopharmaceutical industry.
  • A minimum of 3 years of CRO experience.
  • Strong communication skills.
  • Extensive experience with management of multinational/ international clinical trials.
  • Proficiency in working with complex design issues (e.g., multiple arms, crossover, double blind, and multi-center) in all phases of pre-approval clinical trials.
  • Experience with contributing to proposals, budgets and Bid Defense Meetings for new opportunities.
  • Experience with financial planning.
More About Our Client

A newly appointed CEO brings a fresh vision and an abundance of new approaches for this growing, well-connected CRO.

Are you looking to make an impact on medicine and patient lives? Join this progressive and innovative organization rooted in science, providing end-to-end CRO services in specific therapeutic areas and sought-after SMO services.

Employees have the flexibility to work from home, the office or a combination of the two.

Application process

We go beyond traditional recruitment; we work closely with you to ensure an unrivaled, personal candidate interview experience throughout our entire process.

Our long-standing relationship with this particular client allows us to fully support you through the recruitment process, providing you with all the role insight and knowledge you need for this 2 part interview process.

Our recruitment process is entirely confidential. Your details will never be shared without your prior consent.

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