Senior Manager Salary at Intevity BETA

Position Overview The Sr.Manager, Clinical Data Management will be responsible for performing activities that help to ensure compliance with data quality and documentation standards. This role will perform process and data audits and will trend outcomes to identify quality or training gaps. This role will engage with Data Management vendor staff to provide feedback as necessary. He/She will work closely with Clinical Data Management to support the development and QC of UAT scripts for EDC and eCOA systems and will be the main resource that will execute the study level UAT for these systems. The Manager, Clinical Data Management will also be responsible for the Internal Data Review process at Bicara. He/She may also function as a Study Data Manger as required. Responsibilities Creates Bicara specifications for internal study team data review plans Leads or helps to facilitate internal study team in data review; Performs audits to ensure that the internal and DM Vendor staff complete

Join us as we work to create a thriving ecosystem that delivers accessible, high-quality, and sustainable healthcare for all. Position Summary: As a key member of the Customer Onboarding Business Transformation team, the Enablement and Quality Excellence (EQE) Leader is responsible for developing and implementing a strategic framework to enable and empower Customer Onboarding teams to deliver an exceptional onboarding experience. This role will play a pivotal part in enhancing service delivery quality, fostering cross-functional collaboration, and ensuring that all onboarding resources are equipped with the knowledge, tools, and support needed to achieve measurable success. The Senior Manager will drive initiatives that prioritize employee development, build accountability, and establish high-quality standards across the Customer Onboarding function. By focusing on enablement strategies and data-driven insights, this position will ensure a seamless and value-driven experience for custo

Fusion Pharmaceuticals, a member of the AstraZeneca Group, is a clinical-stage oncology company focused on developing next-generation radioconjugates (RCs) as precision medicines. Fusion connects alpha particle emitting isotopes to various targeting molecules to selectively deliver the alpha emitting payloads to tumors. Fusion’s clinical portfolio includes: FPI-2265 targeting prostate specific membrane antigen (PSMA) for metastatic castration resistant prostate cancer currently in a Phase 2 trial; FPI-1434 targeting insulin-like growth factor 1 receptor currently in a Phase 1 trial; FPI-2059, a small molecule targeting neurotensin receptor 1 (NTSR1), currently in a Phase 1 trial; and FPI-2068, a bispecific IgG-based EGFR-cMET targeted radioconjugate currently in a Phase 1 trial. In addition, Fusion is pursuing combination programs between RCs and DNA Damage Response Inhibitors (DDRis) and immune-oncology agents. Fusion has a fully operational Good Manufacturing Practice (GMP) compliant

JOB TITLE: Senior Manager, Commercial GMP Quality DEPARTMENT: Quality Assurance REPORTS TO: Director, QA LOCATION: Boston / Hybrid – T, W, TH in Seaport DATE PREPARED: December 31, 2024 JOB SUMMARY: The Senior Quality Manager, Commercial Quality at AVEO Oncology reports to the Director Quality Assurance and is responsible for Quality Operations at AVEO. Primary responsibility includes quality oversight and compliance activities related to the cGMP manufacture and release of AVEO commercial products. The successful candidate will be responsible for interfacing with global contract development manufacturing organizations (CDMOs) and providing quality approval of deviations, CAPAs, and change controls while ensuring activities are performed according to applicable guidelines and regulations. The Senior Quality Manager will have responsibility for commercial batch disposition and ongoing continuous improvement initiatives. PRINCIPAL DUTIES: • Quality Operations and Batch Disposition: o Pro

Manager of Logistics, 3PL Provider Management The Opportunity: Contribute To the Growth of Your Career. Be part of a team that leads strategic development of Third Party Logistics providers who operate more than 24 Service Centers (including associated transportation), 15 Transload/Consolidation locations, and 3 Ocean Carriers (PR/HI). Additionally this person is also responsible for the relationship management and procurement for Yard Services. Responsible for assessing and driving cost-effective and productive 3rd party carrier initiatives that impact the supply chain, ensuring seamless execution in supporting and enabling TJX business goals. Responsibilities: Identifies opportunities to improve TJX Logistics Provider strategy, inclusive of Logistics Provider performance, market trends, and demand shifts in the marketplace Builds and maintains relationship with 3PL Providers and serves as point of contact Meets regularly with 3PL partners to discuss forecasts and capacity information

Quality Control Senior Manager Do you have experience developing and maintaining quality standards and processes? Are you looking for an opportunity to enforce Current Good Manufacturing Practices (cGMP) in a contract manufacturing facility? Fraser Dove International is working exclusively with an established biologics organisation specialising in pioneering therapies and new medicines. Our client is seeking a hands-on individual to provide oversight in a manufacturing facility, ensuring that the Quality remains high and cGMP is adhered to. Discover more about our Quality Control Senior Manager opportunity; its objectives, duties/responsibilities and the skills, experience and competencies needed to succeed. Your objectives: As the Quality Control Senior Manager, you will be measured against the following objectives: 1) Supervising the day-to-day operation of the Quality Control function. 2) Serving as a subject matter expert in terms of processes and cGMP. 3) Ensuring that business go

Position Scope: This role supports the regulatory registration of Anika’s products worldwide and contributes to global expansion business plans by assessing regulatory requirements in various international markets for company’s products. The Senior Manager, International Regulatory Affairs collaborates with associates outside the US and EU to achieve rapid worldwide registration of products by providing all documents needed for such efforts and supports continued registration of marketed products on a worldwide basis. This role works with the Regulatory Affairs department to standardize processes and procedures and work on process improvements to streamline registration request completion. Responsibilities: Establishes strategy and manages international registration activities for Anika’s targeted international markets Collaborates with Business Leads to achieve rapid worldwide registrations Supports continued registration of marketed products on a worldwide basis Identifies and commun

Ocular Therapeutix, Inc. (NASDAQ:OCUL) is a biopharmaceutical company focused on the formulation, development, and commercialization of innovative therapies for diseases and conditions of the eye using its proprietary bioresorbable hydrogel-based formulation technology, ELUTYX™. Ocular Therapeutix has built a robust product pipeline of drug delivery solutions developed to reduce the complexity and burden of the current standard of care and position itself to become a leader in the ophthalmic space. Outside of the ophthalmic realm and behind the doors of our headquarters in Bedford, MA, we strive to build a strong culture where employees can flourish and achieve their career goals. We encourage out of the box thinking, cross-functional collaboration, and creativity. As the Senior Manager Strategic Sourcing and Procurement, you will be a part of a fast-growing and innovative ophthalmology organization at the company’s headquarters in Bedford, MA. The role is part of the Supply Chain orga