VP Development Leader, VP Development Leader (late stage) is a critical leadership role within company, reporting to the Chief Medical Officer (CMO) and working closely with the Leadership Team to build a fit-for-purpose Clinical Development organization that delivers differentiated medicines of value that will save, extend, and improve the lives of cancer patients. Key accountabilities and responsibilities * Bui
Global Pharmaceutical and Biotech company is hiring a Senior Project ManagerThe Senior Project Manager will provide day-to-day project management leadership to global drug development project teams. The position will work closely with the Global Program Leaders to establish and maintain project plans and budgets, organize and lead project team meetings, foster communication and coordinate between functional groups. T
MSL needs in North East and North Central region of the USA. This global pharmaceutical company is pioneering a new class of antifungal compounds to help millions of patients worldwide in need of new options to overcome and prevent difficult-to-treat, drug resistant, and recurrent fungal infections. Our passion for the patient is the core foundation of our company. We use our resourceful mindset and agility to drive
Bioinformatics Scientist My well-funded biotech client is expanding and seeks a Bioinformatics Scientist to support their cancer immunotherapy team. The ideal candidate will take on the following tasks: * Develop and optimize NGS-based software including variant calling, gene expression, epigenetic analyses, single-cell sequencing * Integrate diverse NGS and non-NGS data sets to identify cancer drivers, predictiv
Sr. Quality Manager to develop and implement local quality program to support KPIs. Responsible for the quality and safety of our products including HACCP, GMP, GLPs along with the safety of team members and customers. You will also be responsible for the financial management of the annual laboratory budget, laboratory operational performance, reliability of analyses, laboratory instrument maintenance and calibration
Sr Director, Clinical Development My client is expanding and seeks a Sr Director, Clinical Development to take on the following tasks: * Direct clinical trials throughout the clinical trial design, ensuring timely execution and completion of the studies and providing medical, regulatory, and technical guidance throughout the process. * Draft and manage clinical content of all clinical and regulatory documents, en
SENIOR PROJECT TOXICOLOGIST Sr. Research Scientist II, Non Clinical Safety and Pathobiology Associate Director and also Director level available Key Aspects: The Sr. Project Toxicologist works in a project team-based research structure to lead and collaborate with new and ongoing projects. Serves as a nonclinical safety development resource, working with other members of the department regarding strategy for nonc
We are looking for a Quality Assurance Generalist I (QAG I) who will report to the Quality Assurance Supervisor and be responsible for the daily Quality Assurance support in the Manufacturing and Packaging process on site. They will be required to review all appropriate documents during the production process. In this role, the QAG I will be readily available to support the production process; therefore, this positio
We are looking for a Quality Control Chemist at a pharmaceutical manufacturing company. This candidate will need to to stay current on publications released by USP, FDA and other pertinent regulating bodies to ensure the Quality Control Chemistry Laboratory complies in the areas of analytical applications, release specifications, and documentation practices. Quality Control Chemist's Responsibilities: * The Quality
Medical Affairs Scientist, Snr Mgr Position Overview: The Medical Affairs (MA) Scientist will be a member of the MA Strategy and Research team. The position will contribute to the execution of programs during development, launch, and post approval for company products. This includes programs for, but not limited to, investigator initiated trials (IITs), cooperative group studies, registries and post-approval res
