Associate Director, Statistical Programming Bardi

Associate Director, Statistical Programming
Bardi
Emilia Romagna, Bardi

Social network you want to login/join with: Associate Director, Statistical Programming, Metropolitan City of Milan Client: TFS HealthScience Location: Metropolitan City of Milan, Italy Job Category: Other EU work permit required: Yes Job Reference: 87b6ac681572 Job Views: 3 Posted: 02. 03. 2025 Expiry Date: 16. 04. 2025 Job Description: TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions. Join Our Team as an Associate Director, Statistical Programming - home based in UK, Italy or Sweden. About this role As part of our Global Biometrics team, you will work alongside passionate and innovative professionals to ensure our customers achieve their goals. The Associate Director, Statistical Programming is responsible for assisting the Director in leading biometric operations within related departments - Statistical Programming. Key Responsibilities: Assist the Director in strategic planning, leading initiatives, and resource allocation for the department. Participate by offering oversight across studies and/or customers including guidance on documentation and output development/review. Assist the Director in proposal development, project allocation, budget projections, and client presentation, as needed. Serve as a resource for the department, ensuring scientific integrity in the application of statistical methodology to clinical trials. Manage staff in accordance with organization's policies and applicable regulations. Oversee development of direct reports by planning, assigning, and directing work, setting goals, appraising performance, mentoring, and guiding professional development while working with the Director to address any issues. Ensure high quality, timeliness, and expert review process of the deliverables from the department. Provide advanced technical expertise for internal and external clients. Maintain knowledge and awareness of developments in Biostatistics and clinical trial methodology, and regulatory requirements that impact analyses. Accountable for the project level work of staff including awareness of timelines, scope, and resourcing strategy. Responsible for guiding leads toward financial success at a study level. Provide feedback to draft strategy and initiatives. Implement strategy and initiatives and collect feedback from the implementation (e. g. , metrics). Develop and/or provide training to staff across the business unit. Ensure compliance with strategy and initiatives. Qualifications: A Bachelor of Science (BSc) or Master's degree in statistics or related discipline; PhD in Statistics or related discipline preferred or equivalent. Minimum of 10 years relevant statistical experience in pharmaceutical or CRO industry with increasing levels of responsibility. Familiarity with most complex statistical methods that apply to Phase I-IV clinical trials. In-depth knowledge of applicable clinical research regulatory requirements, i. e. , Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Strong working knowledge of SAS, CDISC and Regulatory Submissions. Experience in project management, problem-solving and team leadership. Ability to deal effectively with sponsors and internal customers at all levels. Willingness and ability to travel on occasion. Excellent verbal and written communication skills in English. What We Offer: We provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and professional growth in a rewarding environment. You'll be joining a team that values collaboration, innovation, and making a difference in the lives of patients. A Bit More About Us: Our journey began over 27 years ago in Sweden, in the city of Lund. As a full-service, global Contract Research Organization (CRO), we build solution-driven teams working towards a healthier future. Bringing together over 800 professionals, TFS delivers tailored clinical research services in more than 40 countries with flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology, Neuroscience, Oncology, and Ophthalmology. Our core values of Trust, Quality, Passion, Flexibility, and Sustainability are our guiding light serving as the framework for decision-making at all levels of the organization. They assist us in attracting and retaining valuable talent who share our sentiments, resulting in high employee engagement and satisfaction. By aligning on these fundamental values, we cultivate a unified force, geared towards innovation and excellence. This collective effort propels us towards our shared goal and fosters a culture of mutual respect and collaboration. Together we make a difference. J-18808-Ljbffr