Job Description

NAMSA is a Medical Research Organization (MRO), accelerating product development through integrated laboratory, clinical and consulting services. Driven by our regulatory expertise, NAMSA’s MRO® Approach plays an important role in translational research, applying a unique combination of disciplines—consulting, preclinical, toxicology, microbiology, chemistry, clinical and quality—to move client’s products through the development process, and continue to provide support through commercialization to post-market requirements, anywhere in the world.

In order to support our expansion, we are growing our team and are currently looking for YOU to join our team as

Your responsibilities :

• Serves as key liaison with client, including communications in critical and high-profile discussions with upper and executive level management
• Provides direction to cross-functional teams while managing complex projects
• Understands the complexity of multiple moving pieces within the project execution, motivates the team and collaborates with the client to adjust plans in order to optimize performance
• Persuasively influences client and internal stakeholders to ensure project deliverables are completed with high quality, on time, and within budget
• Handles challenging situations with the client, and knows when to escalate issues to management
• Manages financial aspects of projects according to the statement of work
• Responsible for the technical and regulatory accuracy of proposals they generate, including an understanding of the intended clinical use of the test article being quoted
• Other duties are assigned

Your qualifications:

• Bachelor’s degree in a related area and 4-6 years of experience in medical device, clinical, regulatory, project management or related areas
• Mastery of project management tools, processes, practices and procedures
• Demonstrated ability to establish and maintain relationships with clients and internal Associates
• Working knowledge of standards, sales and proposals
• CAPM or PMP certification preferred
• Experience with Good Laboratory Practice (GLP), Good Clinical Practice (GCP) and Good Manufacturing Procedures (GMP) preferred
• Fluency in English and local language, if different, required

We offer:

• A challenging and varied job in a globally expanding company
• A highly professional team and an international working environment
• Attractive, performance-related remuneration
• Flexible working hours
• Pension plan
• Team events

This position is based in Germany, UK or US and is remote.