Agency Director Salary at Soladis Gmbh BETA

The YWCA Cambridge is dedicated to eliminating racism, empowering women and promoting peace, justice freedom and dignity for all. Position Summary: The Housing and Stabilization Case Manager reports to the Family Shelter Director and is a member of the Housing and Shelter Services Team and performs service based on the "Housing First" philosophy. The Housing and Stabilization Case Manager works individually with families to sustain permanent housing and the services to maintain housing The Housing and Stabilization Case Manager is responsible for placing families into stable housing, as outlined in the EOHLC contract, by exploring all potential housing outcomes. Once established, the Housing and Stabilization Case Manager will continue to work with families for up to 24 months to ensure that families will remain stabilized. Essential Functions: Responsibilities include but may not be limited to the following. Rehousing Activities: Implements a Rehousing and Stabilization Plan within te

Statement of Duties The Director of Housing oversees the City's policies and programs to create and preserve affordable housing and stimulate market rate housing, including the provision of various housing services to improve the quality of the City's housing stock and to meet the housing needs of Somerville residents. Employee is required to perform all similar or related duties. Essential Functions: The essential functions or duties listed below are intended only as illustrations of the various type of work that may be performed. The omission of specific statements of duties does not exclude them from the position if the work is similar, related, or a logical assignment to the position. Develops policies and programs to create and preserve affordable housing and stimulate market rate housing. Projects evaluation of housing development including those subject to restrictions under state and federal grant programs and those subject to inclusionary housing implementation plans. Tracks,

Position Summary: The Associate Director, Commercial Regulatory Affairs leads the review and approval of promotional and medical communications for assigned brands. The role involves interacting with regulatory bodies like the FDA, ensuring compliance with regulations, and guiding internal teams through promotional material development. This position requires collaboration with multiple departments, including legal and business ethics, to ensure products' promotional communications meet all required standards. Key Responsibilities: Provide regulatory advice on FDA advertising and promotion issues for assigned products. Lead and manage the Promotional Review Committee (PRC) process and ensure materials meet regulatory standards. Develop and implement standard operating procedures (SOPs) to streamline processes. Liaise with regulatory agencies for product submissions and compliance. Collaborate with cross-functional teams to integrate regulatory guidance into business strategies. Manage

Description Synagro is North America's premier, award-winning, biosolids management firm offering a competitive salary for highly motivated, self-starter with strong work ethic, in a supportive work environment. Synagro partners with stakeholders to clean our water, protect our environment and serve our communities by generating worth from what others call waste. We work to protect the health of our water, our Earth, and those who depend on them now and in the future. What good is a job without great benefits to reward your hard work? Here are some highlights of what Synagro has to offer: 15 days paid time off 10 holidays Medical/Dental/Vision (within 30 days of hire) Health Savings Account (HSA) with company match Flexible Spending Account (FSA) 401(k) with company match, (fully vested upon hire) Career growth and promotional opportunities Tuition Reimbursement Bonus Incentive Program JOB SUMMARY This position can be a remote position. Under the direction of the Area Director, this ro

Objective / Purpose: Defines, develops and leads global strategies to maximize global regulatory success towards achievement of program objectives for complex and/or multiple projects. Provides strategic and tactical advice to teams to achieve timely and efficient development and maintenance of programs, while ensuring compliance with applicable regulatory requirements. Is a leader both in the department and within R&D, leading and/or contributing with influence to cross-functional initiatives and influencing the field as applicable. Provides leadership and development for direct reports, including those that serve as global regulatory leads responsible for the design and execution of global regulatory strategies in collaboration with their regional counterparts. Accountabilities: The Senior Director will be responsible for complex or highly complex or multiple projects. Leads the Global Regulatory Teams (GRTs) and applicable sub-working groups, such as the Label Working Group, and rep

Objective / Purpose: Defines, develops and leads global strategies to maximize global regulatory success towards achievement of program objectives for complex and/or multiple projects. Provides strategic and tactical advice to teams to achieve timely and efficient development and maintenance of programs, while ensuring compliance with applicable regulatory requirements. Is a leader both in the department and within R&D, contributing to cross-functional initiatives and influencing the field as applicable. Provides leadership and development for direct reports, including those that serve as global regulatory leads responsible for the design and execution of global regulatory strategies in collaboration with their regional counterparts. Accountabilities: The Director will be responsible for complex or highly complex or multiple projects. Leads the Global Regulatory Teams (GRTs) and applicable sub-working groups, such as the Label Working Group, and represents GRTs at project team meetings

Director eTMF - Permanent - Cambridge, MA Proclinical is seeking a Director for the electronic Trial Master File (eTMF) team. Primary Responsibilities: The successful candidate will lead the eTMF team, ensuring that all activities are managed effectively and that the Trial Master File is always ready for inspection. This position focuses on maintaining high-quality documentation and compliance with regulatory standards. Skills & Requirements: Bachelor's degree or equivalent in information management, library science, clinical science, or related field. Extensive experience with Veeva Quality systems and training eTMF staff. Experience in TMF management for global clinical trials. Familiarity with computerized clinical trial records management technologies, especially Veeva systems. Proven personnel management experience with team development skills. Strong organizational, writing, and communication abilities. Advanced knowledge of ICH/GCP guidelines, FDA regulations, and international

Senior Director/Vice President Development Project Leader Repertoire Immune Medicines is a biotechnology company working to unlock and direct the remarkable power of the human immune system to treat cancer and autoimmune disease. The company was founded on the belief that understanding the repertoire of T cell receptor (TCR)-antigen immune synapses that maintain health and drive disease represents one of the greatest opportunities for innovation in medical science. Repertoire scientists created and developed the DECODETM platform, which allows in-depth characterization of TCR-antigen pairs, and the ability to deploy this information in the form of novel targeted immune medicines to fundamentally reprogram the immune system to kill tumors or induce immune homeostasis. From its sites in Cambridge, Massachusetts and Zurich, Switzerland, Repertoire’s team is advancing a pipeline of DECODE-enabled immune medicines. For cancer, we are developing a pipeline of TCR bispecifics molecules for tr