Assist in the development and implementation of publication planning across therapeutic area(s) in collaboration with Senior leaders of Scientific Communications and Training, Biometrics, Research and Development, Operations, Medical Science Liaisons (MSLs), Therapeutic area Medical Leads, HEOR, and other appropriate functions. Contribute to the development, implementatio

Perform routine cleaning and sanitization of cleanroom areas, equipment, and surfaces following established protocols and Standard Operating Procedures (SOPs). Wipe down and disinfect surfaces, walls, floors, and ceilings to maintain a sterile and contaminant free environment. Remove waste, debris, and used materials from cleanroom areas, disposing of them properly in des

Develop, implement and execute the facilitation of Ferring core curriculum programs and create new account based programming annually or more frequently. This includes but not limited to new hire onboarding support, post onboarding support, brand strategy execution, individualized learning needs and regional based needs as identified by sales leadership. Work with sales l

Drive launch performance of ADSTILADRIN across our key customers Collaborate closely with multiple internal business partners Create a winning culture and coach staff on the team Create a highly collaborative and effective cross functional marketing team that strives for flawless execution that results in an optimal customer experience Develop marketing strategy, leading

Assist production management in the execution of setup activities to ensure efficient, timely and smooth operations. Set up, operation of and assessing/resolving equipment mechanical problems of all GMP equipment and utilities in the Controlled Classified and non Classified Production/utility areas (A/B, C, D, clean utility area and packaging area) including but not limit

US Regulatory TA Strategy Lead the development and execution of US regulatory strategy in conjunction with Global Regulatory Lead (GRL), Global Regulatory Team and Global project teams. Partner with the GRL to understand the competitive landscape, e.g., views of US HAs, regulatory precedents, labeling differences and TA specific issues. Utilize US regulatory expertise and

US Regulatory TA Strategy Develop and execute US regulatory strategy, with oversight as needed, and in conjunction with Global Regulatory Lead (GRL), Global Regulatory Team and Global project teams. Partner with the GRL to understand the competitive landscape, e.g., views of US HAs, regulatory precedents, labeling differences and TA specific issues. Utilize US regulatory

Perform method qualification and participate in analytical assay transfer to ensure successful start up of laboratory. Performs compendia method qualifications. Executes analytical and wet chemistry methods using HPLC, FTIR, GC, UV Vis, and other instruments. Execute stability program including pulling, testing and report generation. Perform routine water testing. Monitor

Support and maintains clinical data management processes and data capturing systems for clinical trials by following Ferring SOP Support CRFs development, data mapping specifications, DVP, DMP, and data transfer specifications and tests EDC system functionalities. Participates in cross functional clinical trial teams and communicates data management matters effectively. T

Create and deliver the advanced analytics short and long term road map both at Brand and Enterprise level. Collaborating with analytics and cross functional partners, assess, optimize, and drive advanced analytics initiatives (such as HCP/Account/Payer/Patient segmentations, Predictive Targeting, Key Driver Analysis, Omni Channel Investment Optimization, Patient Journey e

Collaborate with members of the CLO team and business partners to continuously seek out and lead process improvement initiatives that further the implementation of the CLO Services Model. Identify data within CLO, Ferring, and third party systems and processes that can be used to drive continuous improvement of CLO services. Implement continuous improvement in CLO service

Oversight Lead the overall management of study execution utilizing available performance metrics and quality indicators. Ensure development, management and maintenance of study budget, timeline, and deliverables. Responsible for timely escalation of issues internally to team and management, as appropriate. Financial planning and management. Ensure clear delegation of task

Works closely with the GM and other assigned business leader(s) to enable business growth and performance through understanding the overall business strategy, developing relevant HR strategies and executing against them. Leads change management, engagement and retention initiatives in partnership with the Uro Oncology leadership team, leveraging the Ferring leadership Pri

1. Identify optimal clinical data management (CDM) solutions for capturing, integrating, and processing clinical data from different sources (e.g., eCRF, ePRO, eCOA, central laboratory); 2. Provide end to end CDM support by specifying CRF metadata using Trial Definition Tool, EDC functionalities, data validation/transfer specs and CDM plans; by implementing data visualiza

CMC Regulatory Strategy Partner with key stakeholders to develop and implement CMC regulatory strategies and plans for CMC projects. Develop solutions to regulatory or business problems where no clear precedence exists. Submissions for Development and Commercial Products Lead activities, including planning and reviewing US CMC sections of all regulatory submissions (i.e.