Deciphera Pharmaceuticals

We are seeking a results-oriented innovative broadly experienced CMC leader who will lead and manage Decipheras Analytical Development & Quality Control organization. The incumbent will continue to build and develop a team with technical competencies in method development and QC t More...

The Role:The Senior Clinical Project Manager leads and manages a more complex clinical studies demonstrating a higher level of knowledge of clinical operations methodologies stronger organizational project management and leadership capabilities as well as increase strategic insight de More...

Position Summary: Deciphera B.V. is seeking a Sr. Director Global QPPV to oversee pharmacovigilance activities for medicinal products in the EU/UK and other global countries. The role involves ensuring compliance with legal requirements maintaining the Pharmacovigilance System Master More...

Deciphera is seeking a Manager Commercial Finance to be based in Waltham MA the companys headquarters. The Manager Commercial Finance will support the companys Commercial Finance function to support the companys current products on the market QINLOCK  and ROMVIMZA and prepare for More...

Deciphera is seeking a Manager Gross Margin to be based in Waltham MA the companys headquarters. The Manager Gross Margin will support the companys Commercial Finance function to support the companys current products on the market QINLOCK  and ROMVIMZA and prepare for multiple pr More...

The Role:We are seeking an Associate Director in Regulatory CMC who can independently lead contribute and execute on CMC regulatory activities in support of Decipheras studies across all stages of clinical drug development.  The primary responsibility will be to generate high qua More...

We are seeking a Medical Director. This position will report to the Senior Medical Director of Pharmacovigilance and will be located in the Waltham office.The Medical Director is responsible for global pharmacovigilance (PV) for marketed and/or investigational products including revie More...

The Role:We are seeking an Associate Director in Regulatory CMC who can independently lead contribute and execute on CMC regulatory activities in support of Decipheras studies across all stages of clinical drug development.  The primary responsibility will be to generate high qua More...

The Role:We are seeking an Associate Director in Regulatory CMC who can independently lead contribute and execute on CMC regulatory activities in support of Decipheras studies across all stages of clinical drug development.  The primary responsibility will be to generate high qua More...

Responsibilities:Develop and lead a strong key customer engagement strategy in close partnership with the Sarcoma Brand TeamsPlan and execute key customer insight gathering initiatives including advisory boardsLead strategy planning and execution of KOL engagement initiativesLead peer More...

The Role:The Senior Clinical Project Manager leads and manages a more complex clinical studies demonstrating a higher level of knowledge of clinical operations methodologies stronger organizational project management and leadership capabilities as well as increase strategic insight de More...

The Role:The Senior Clinical Trial Associate (Sr. CTA) supports the management of the clinical trial from initiation to completion while partnering with internal and external crossfunctional disciplines. The Sr. CTA assists in supporting the conduct and processes of trials including p More...

We are seeking a resultsoriented innovative broadly experienced CMC leader who will lead and manage Decipheras Analytical Development & Quality Control organization. The incumbent will continue to build and develop a team with technical competencies in method development and QC to More...

We are seeking a Senior Manager in Regulatory CMC who can independently lead contribute and execute on CMC regulatory activities in support of Decipheras studies across all stages of clinical drug development.  The primary responsibility will be to generate high quality and compl More...

We are seeking a Medical Director. This position will report to the Senior Medical Director of Pharmacovigilance and will be located in the Waltham office.The Medical Director is responsible for global pharmacovigilance (PV) for marketed and/or investigational products including revie More...

The Role:The Clinical Trial Associate (CTA) is responsible for assisting and providing support to the members of the clinical operations project team to support the management of clinical trials from initiation to completion while partnering with internal and external crossfunctional More...

The Role:The Senior Clinical Trial Associate (Sr. CTA) supports the management of the clinical trial from initiation to completion while partnering with internal and external crossfunctional disciplines. The Sr. CTA assists in supporting the conduct and processes of trials including p More...

Position Summary: We are seeking a dynamic Senior Manager Program Management to support and drive our clinical programs. You will utilize your project management skills to ensure programs are operationally on track establish best practices and contribute to special projects. This role More...

The Associate Director Regulatory Affairs will join a group of highly motivated topnotch regulatory professionals and will be a key player in shaping cohesive regulatory strategies across the product pipeline. This role provides regulatory support for oncology products in earlystage a More...

We are seeking a talented collaborative and highly motivated individual to join our Biological Sciences oncology drug discovery group. This role involves working closely with a multidisciplinary research team to discover new small molecule therapeutics for cancer treatment.Responsibil More...