Clinical Trials Coordinator

Job OverviewThe Clinical Trial Assistant will play a crucial role in supporting the clinical research team at TN Sweden. This position is responsible for providing administrative support to ensure the smooth execution of clinical trials.

Role OverviewThe Scientific Evidence Partner is a key position in our organization, responsible for generating scientific knowledge and executing clinical trials. This role requires strong partnering skills, innovative thinking, and the ability to implement sustainable solutions for healthcare and Roche.This specialist will be accountable for delivering...

**Research Operations Coordinator**This position is responsible for supporting the day-to-day operations of our research team. The Research Operations Coordinator will assist with site activation, document preparation and data management.**Key Responsibilities**Assist with site activation activities and document preparationManage research documentation and...

Key ResponsibilitiesCreate innovative delivery strategies and solutions for Cardiovascular trials or studies, addressing customer needs and challenges.Partner with internal stakeholders to award strategic and tactical new business, achieving annual Gross New Business targets.Provide scientific, clinical, and operational advice to develop proposals, including...

**About Cellcolabs**We are a biotech impact start-up dedicated to promoting advanced cell therapies to improve health. Our mission is to drive the availability of mesenchymal stem cells (MSCs) by lowering their price for research and clinical use in the future.About the RoleWe are seeking a medical doctor with a strong background in stem cells,...

**Job Overview**We are a Swedish biotech company that utilizes advanced cell therapies to promote better health outcomes. As a Medical Doctor with a strong background in stem cells, you will have the opportunity to contribute to our mission and make a difference in medicine.ResponsibilitiesTo conduct consultations with individuals interested in participating...

Key ResponsibilitiesAssist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) teams with maintaining accurate and up-to-date clinical documents and systems, including the Trial Master File (TMF).Prepare, handle, distribute, file, and archive clinical documentation and reports according to standard operating procedures.Support CRAs and RSU...

**Site Activation Lead**This position is responsible for the successful execution of site activation activities across multiple clinical trials. The Site Activation Lead will work closely with investigators, monitors and other stakeholders to ensure seamless site initiation and maintenance.**Key Accountabilities**Develop and implement effective site...

Responsibilities and ExpectationsSupport CRAs and RSU teams in maintaining clinical documents and systems.Prepare and distribute clinical documentation and reports.Support the clinical team with tracking and managing CRFs, queries, and clinical data flow.Act as a central contact for the clinical team.Participate in site visits to assist with clinical...

**Job Overview**The Regulatory Affairs Manager will be responsible for ensuring that all regulatory requirements are met across our clinical trials. This includes maintaining accurate records and communicating with site staff and project managers.**Key Responsibilities**Maintain up-to-date knowledge of local and international regulationsEnsure compliance...

About the RoleThis is an exciting opportunity for a seasoned physician with experience in Cardiology to lead our medical strategy efforts in Cardiovascular development. You will work closely with our indication-specific teams to develop integrated strategies for clinical trials and studies.

Overview of the Research GroupOur research team is dedicated to studying the complexities of viral pathogenesis and the immune system's response to tick-borne encephalitis virus (TBEV). With a focus on translational research, we combine experimental virology and immunology with ex vivo studies and clinical trials. Our goal is to gain a deeper understanding...

Job OverviewThe Regulatory Affairs Associate is responsible for overseeing a range of regulatory activities for assigned medicines, medical devices, cosmetics, and/or food supplement consumer products within their geographical and/or brand area of responsibility.Compiles and submits applications (post-approval and new submissions), resolves Health Authority...

Join our team at TN Sweden as a Medical Advisor and contribute to advancing medical knowledge and improving patient outcomes! We are seeking a highly skilled professional with experience in the field of neuroscience to join our medical affairs group.Responsibilities:Develop and maintain expert scientific knowledge within the assigned therapeutic...

TN Sweden is a leading company in the field of neuroscience, and we are seeking a Medical Advisor to join our team. As a key member of our medical affairs group, you will represent the Swedish affiliate's medical/scientific voice of expertise for assigned products in the field of neuroscience.Key Responsibilities:Attend scientific congresses, arrange...

Are you passionate about advancing medical knowledge and improving patient outcomes? Do you have experience in the field of neuroscience?We are seeking a Medical Advisor to join our team at TN Sweden, working closely with experts and academic centers to establish and maintain professional relationships. This role involves delivering scientific presentations...

Company OverviewTN Sweden is a leading pharmaceutical company dedicated to improving lives through innovative medical solutions. As a Medical Advisor in Neuroscience, you will be part of our team that strives to make a difference in the field of therapeutic neurotoxins.Job DescriptionWe are seeking an experienced Medical Advisor to work with our portfolio in...

At TN Sweden, we are seeking a Medical Advisor to join our team in the field of neuroscience. As a key member of our medical affairs group, you will represent the Swedish affiliate's medical/scientific voice of expertise for assigned products in the field of neuroscience.Key Responsibilities:Establish and maintain professional relationships with experts and...

Key ResponsibilitiesSite Selection and Sizing: Support site selection and sizing while developing the business case for prospective sites.Activating Sites: Activate sites and establish relationships with key partners and decision-makers.Tactical Implementation: Facilitate the transition of clinical sites into certified sites, lead tactical implementation of...

Vi söker en oerhört duktig och ansvarstagande Quality Assurance Specialist för vår radiofarmaciverksamhet. Din huvudsakliga uppgift kommer att vara att arbeta med olika kvalitetsrelaterade uppgifter inom den laborativa verksamheten, inklusive frisläppning av radiofarmaka samt hantering av produktions- och laboratoriemiljöavvikelser.Vad erbjuder vi?En...