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 Provider (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 of Statistical Programming is responsible for assisting the Director in leading biometric operations within the Statistical Programming department. Key Responsibilities Assist the Director in strategic planning, leading initiatives, and resource allocation for the department. Provide oversight across studies and/or customers, including guidance on documentation and output development/review. Manage staff in accordance with organizational policies and applicable regulations. Oversee the development of direct reports by planning, assigning, and directing work, setting goals, appraising performance, mentoring, and guiding professional development, working with the Director to address any issues. Ensure high quality, timeliness, and expert review of department deliverables. Provide advanced technical expertise for internal and external clients. Maintain knowledge of developments in Biostatistics, clinical trial methodology, and regulatory requirements impacting analyses. Accountable for project-level work of staff, including timelines, scope, and resourcing strategy. Guide leads towards financial success at the study level. Provide feedback on strategy and initiatives. Implement strategies and initiatives, and collect feedback through metrics. Develop and/or provide training to staff across the business unit. Ensure compliance with strategies and initiatives. Qualifications BSc or MSc in statistics or related discipline; PhD preferred or equivalent. Minimum of 10 years relevant statistical experience in the pharmaceutical or CRO industry with increasing responsibilities. Deep knowledge of clinical research regulatory requirements, including GCP and ICH guidelines. Strong working knowledge of SAS, CDISC, and Regulatory Submissions. Experience in project management, problem-solving, and team leadership. Effective communication skills in English, both verbal and written. Willingness and ability to travel occasionally. What We Offer Competitive compensation, comprehensive benefits, and opportunities for growth in a rewarding environment. Join a team that values collaboration, innovation, and making a difference in patients' lives. A Bit More About Us Founded over 27 years ago in Lund, Sweden, we are a full-service, global CRO with over 800 professionals operating in more than 40 countries. We specialize in therapeutic areas including Dermatology, Neuroscience, Oncology, and Ophthalmology. Our core values—Trust, Quality, Passion, Flexibility, and Sustainability—guide all our decisions and actions, fostering a culture of respect, collaboration, and excellence. Together we make a difference. J-18808-Ljbffr J-18808-Ljbffr