Tfs Trial Form Support AB

TFS HealthScience is a global contract research organisation partnering with pharmaceutical and biotech companies to take new therapies through clinical development. Behind every study are people, and we are looking for an HR Business Partner who wants to make sure we have the right ones, in the right roles, ready for what comes next. The role As our HR Business Partner, you will work side by side with senior leaders as a trusted advisor, and you will have a real say in how our business grows. You see HR as a business lever: you understand what drives revenue, and you make sure our people decisions support it. You will also help shape how our HR team works going forward, using modern tools and AI to make HR faster, smarter and more valuable to the business. This role is based at our Lund office, so you will need to live in southern Sweden within commuting distance. What you will do * Partner with leaders on organisational development and change * Shape strategic talent management and workforce planning, so we have the right capabilities for tomorrow's business * Advise leaders on people matters, from performance and conflict to restructuring * Lead succession planning and business continuity * Develop our leaders and help them grow their teams * Handle employment law matters and work with unions and works councils * Strengthen TFS as a place where great people want to work Who you are You understand how a client services organisation grows, what its leaders are accountable for, and how people decisions affect performance and profitability. Leaders turn to you because you are credible, approachable and willing to challenge their thinking. You handle difficult conversations with integrity, respond to immediate needs without losing sight of longer term priorities, and stay open to better ways of working. You build trust across teams and borders in an international organisation. What you bring * Proven experience as an HR Business Partner, advising senior leaders at a strategic level * Academic degree in Human Resources, Business Administration, Psychology, Law, or a related field. * Strong commercial acumen, ideally from a client facing or service based business * Solid knowledge of Swedish employment law * Fluent English and Swedish * Based in southern Sweden, within commuting distance of our Lund office * A genuine interest in using data, digital tools and AI in HR Nice to have * Experience from life science, pharma or a CRO Why join us * Real influence, with direct access to senior leadership * The chance to shape how HR supports a growing international business * An international environment with the agility of a company still building its future * Work that ultimately helps bring new treatments to patients

ABOUT THIS ROLE 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. The Clinical Supply Coordinator (0.1 FTE) is a part-time specialist role responsible for supporting the oversight, planning, and coordination of clinical trial supplies across global studies. Working approximately 10% of a full-time schedule, you will provide expert guidance on investigational medicinal product (IMP) management, supply forecasting, documentation review, and clinical supply strategy to ensure uninterrupted study execution. As part of our SRS/FSP team, you will be dedicated to one sponsor, a global pharmaceutical company that is an industry leader within its therapeutic area. KEY RESPONSIBILITIES * Provide expert support for clinical trial supply activities on a part-time (0.1 FTE) basis. * Review and maintain IMP-related documentation to ensure quality, accuracy, and regulatory compliance. * Support supply forecasting activities to ensure adequate drug availability throughout study execution. * Advise on clinical supply strategy, inventory management, and distribution planning. * Coordinate with depots, vendors, and study teams to address supply-related risks and challenges. * Review supply plans and identify potential shortages, delays, or compliance concerns. * Collaborate with Clinical Operations and other stakeholders to support uninterrupted study conduct. * Ensure supply-related documentation remains inspection-ready and compliant with applicable regulations. QUALIFICATIONS * Bachelor's degree in Pharmacy, Life Sciences, Supply Chain Management, or a related field, or equivalent relevant experience. * Experience in Clinical Supply, Clinical Operations, Drug Supply Management, or Clinical Trial Management within the pharmaceutical, biotechnology, or CRO industry. * Understanding of clinical trial supply processes, IMP management, and GxP requirements. * Experience with supply forecasting, inventory planning, logistics coordination, or vendor management. * Ability to work independently and provide expert guidance in a fractional consulting capacity. * Strong communication, organizational, and stakeholder management skills. What We Offer We provide opportunities for personal and professional growth in a rewarding environment. You will join a team that values collaboration, quality, and making a difference in the lives of patients. Our core values of Trust, Quality, Passion, Flexibility, and Sustainability guide our decisions and shape our culture. By aligning on these values, we foster collaboration, innovation, and a shared commitment to excellence. Together, we make a difference. A Bit More About Us Our journey began over 30 years ago in Sweden, in the city of Lund. As a full-service global CRO, we build solution-driven teams working toward a healthier future. Bringing together over 600 professionals, TFS delivers tailored clinical research services in more than 50 countries, offering flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology, Neuroscience, Oncology, and Ophthalmology.

ABOUT THIS ROLE 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. The Senior Statistical Programmer will provide statistical programming expertise and strategic support to global clinical studies. In this role, you will work closely with cross-functional stakeholders to review and interpret clinical trial data, support statistical analyses, and ensure the quality and integrity of statistical and data management deliverables produced both internally and by external partners. As part of our SRS/FSP team, you will be dedicated to one sponsor, a global pharmaceutical or biotechnology company that is advancing innovative therapies in areas of significant unmet medical need. KEY RESPONSIBILITIES * Develop, validate, and maintain SAS programs for clinical trial reporting and analysis. * Generate and review SDTM and ADaM datasets in accordance with CDISC standards. * Produce and validate Tables, Listings, and Figures (TLFs) for study reports and regulatory submissions. * Review, assess, and interpret clinical study data to support study teams and informed decision making. * Evaluate protocol deviations and contribute to assessments of their potential impact on study outcomes. * Review statistical analyses, datasets, and deliverables generated by external service providers. * Collaborate with Biostatistics, Clinical Operations, and Data Management teams to ensure high quality study execution. * Contribute to data review activities and support the development of analysis specifications and programming documentation. * Support regulatory submissions and ensure statistical deliverables are inspection-ready. * Drive continuous improvement of programming standards, processes, and automation initiatives. QUALIFICATIONS * Bachelor's or Master's degree in Statistics, Biostatistics, Mathematics, Computer Science, Life Sciences, or a related field. * Experience in Statistical Programming within the pharmaceutical, biotechnology, or CRO industry. * Strong SAS programming skills. * Experience with CDISC standards, including SDTM and ADaM. * Experience producing Tables, Listings, and Figures (TLFs). * Solid understanding of clinical trial methodology, ICH-GCP, and regulatory requirements. * Ability to review and interpret clinical data and statistical outputs. * Experience working with external vendors or CRO partners is highly desirable. * Strong communication skills and the ability to collaborate effectively within global cross-functional teams. * Knowledge of Data Management processes and R programming is considered an advantage. WHAT WE OFFER We provide opportunities for personal and professional growth in a rewarding environment. You will join a team that values collaboration, quality, and making a difference in the lives of patients. Our core values of Trust, Quality, Passion, Flexibility, and Sustainability guide our decisions and shape our culture. By aligning on these values, we foster collaboration, innovation, and a shared commitment to excellence. Together, we make a difference. A BIT MORE ABOUT US Our journey began over 30 years ago in Sweden, in the city of Lund. As a full-service global CRO, we build solution-driven teams working toward a healthier future. Bringing together over 600 professionals, TFS delivers tailored clinical research services in more than 50 countries, offering flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology, Neuroscience, Oncology, and Ophthalmology.