Responsible for providing technical leadership and guidance across CMC development disciplines to all outsourced development and manufacturing activities by providing clear objectives for multiple CDMO partners, assess all experimental plans and results, and coordinate future work to achieve desired development and manufacturing expectations
Secure and expand volume of profitable new business contracts. Directs and executes the creation of annual, global/international Strategic Account Plans to maximize profitable sales, maintain high client satisfaction, and bring value to customers.
Reporting to the Chief Product Supply Officer, the Director, Global Logistics is responsible for both short term tactical plan achievement as well as establishing a global logistics strategy and leading the implementation of a scalable global procurement, planning, logistics and fulfillment functions for binx health .
We are seeking to hire an experienced and highly motivated Program Management leader to work with our Clinical Development program teams, and who will report to the Chief Medical Officer. The successful candidate will have strong leadership skills in multidisciplinary teams’ settings with experience of clinical development including first in human (Ph1), proof of concept (Ph2) and pivotal / registrational trials (Ph3).
We are working with them to identify an experienced executive for a Head of Regulatory Affairs. This key leadership position will support all RA related activities required to progress their novel programs through preclinical and clinical development and to ensure alignment within the company and regulatory agencies.
We are working with them to identify a candidate for Head of Clinical Operations. This highly visible will report directly to the Chief Medical Officer and will interact on a regular basis with the broader executive team. The position’s primary responsibilities are focused on several areas including, but not limited to, design and implementation of clinical studies; building and managing relationships with Contract Research Organizations (CROs) and academic collaborators; overseeing the creation and implementation of standard operating procedures for clinical development; contributing to the creation and implementation of the overall clinical strategy.
The Executive Medical Director / VP (ED/VP) will be responsible for leading clinical development programs for the company and will report to the Chief Medical Office. The (ED/VP) will support the strategic, clinical and regulatory aspects of all programs and will serves as the Global Project Medical Lead for clinical and imaging trials in AD, and orphan disorders such as PSP and FTLD, ensuring compliance with ICH/GCP and federal regulations.
Our client is a well-funded and rapidly growing clinical-stage biopharmaceutical company developing novel classes of medicines to treat neurodegenerative diseases, located in Kendall Square, Cambridge MA.
The Senior Scientist, Medicinal Chemistry will be primarily responsible for the design and synthesis of novel small molecules to advance projects through lead ID and lead optimization. In this role, they will be required to manage external resources to deliver on synthetic and analytical tasks and will also work collaboratively with our scientific team and partners in the US and Asia.
Key responsibilities:
The successful applicant will have demonstrated a high level of proficiency in modern synthetic organic / medicinal chemistry as applied to drug discovery and lead optimization. They will work as part of the Medicinal Chemistry team and will be responsible for designing and managing the synthesis of novel compounds to rapidly advance projects to IND filing. For project centric activities, data and progress review, the role will involve close interaction with the Discovery, Biology, and Pharmacology teams.
Tasks include:
Key skills & competencies:
The Executive Medical Director / VP (ED/VP) will be responsible for leading clinical development programs for the company and will report to the Chief Medical Office. The (ED/VP) will support the strategic, clinical and regulatory aspects of all programs and will serves as the Global Project Medical Lead for clinical and imaging trials in AD, and orphan disorders such as PSP and FTLD, ensuring compliance with ICH/GCP and federal regulations.
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