As Marketing Director, one will establish our client as one of the top CDMO/CRO’s in the pharmaceutical, biopharmaceutical and biotechnology markets through implementation of robust strategic and tactical marketing activities. The Director will support our client in attracting and retaining a global customer base and securing a pipeline of clients and projects leading to consistent, sustainable, predictable growth of the business.

As Project Management Director one will direct the development, organization and management of project teams, highlighting achievements, obstacles and risk reduction to senior management. The Director will develop and maintain project timelines, project plans and task deliverables. One will ensure appropriate project management expertise in the planning, execution and close-out of all client-based contracts.

The Director is responsible for end-to-end technical oversight of cGMP manufacturing processes at all stages of the product lifecycle, while maintaining and improving the scientific oversight and technical changes of the manufacturing processes.

This Global Business Insights & Analytics search is being conducted on behalf of our leading biopharmaceutical client who is pushing the boundaries of science to deliver life-changing medicines. They are resetting expectations of what a biopharmaceutical company can be. They are opening new ways to work, groundbreaking and cutting-edge methods and bringing unexpected teams together.

In this role, one will lead the Early Portfolio Global Analytics and Insight team and be responsible for scoping and ensuring delivery of the body of insight and analysis to support and development of early asset, tumor and portfolio strategies.

Our global client is an emerging global leader in cancer treatment with a commercialized device product in targeted therapy. With US offices in the Boston region, we have been retained to identify their Global Director of Clinical Operations. This person will be responsible for the implementation and management of the clinical global research operations, including both pre-and post-marketing clinical trials and new device and/or drug products that they will develop in the future.

We are seeking a management level regulatory affairs individual who wants to advance their career to the next level. Our growing client is extremely innovative and has an expanding and diverse portfolio in infectious disease and oncology.