Clinical Study Assistant

Career Opportunity: Clinical Data Entry Specialist at TFS HealthScienceClinical trials rely heavily on precise data management. As a Clinical Data Entry Specialist at TFS HealthScience, you will play a vital role in supporting pharmaceutical companies in this process.About the PositionYou will be responsible for entering clinical data, anonymizing documents,...

Job OverviewTFS HealthScience is a leading global Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey.We are seeking a highly skilled Clinical Data Entry Specialist to support a high-impact clinical study with one of our key pharmaceutical clients.Key...

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. We are seeking a Clinical Data Entry Specialist to support...

About the RoleWe are looking for a skilled Clinical Data Entry Specialist to join our team in supporting a clinical study.The role involves managing clinical data entry, document anonymization, and uploads to electronic data capture (EDC) systems.ResponsibilitiesEnter clinical data from source documents into an EDC system.Process a backlog of clinical cases,...

TFS HealthScience is a global Contract Research Organization (CRO) partnering with biotech and pharmaceutical companies in their clinical development journey.We seek a Clinical Data Entry Specialist to support a high-impact clinical study with one of our key pharmaceutical clients.About the StudyThis study requires precise data management to ensure accurate...

Job DescriptionThis is a unique opportunity to work as a Clinical Data Entry Specialist with TFS HealthScience, supporting a high-impact clinical study.The role involves working closely with the study team to ensure timely and efficient data processing, while also managing a backlog of clinical cases.Key ResponsibilitiesManage clinical data entry, document...

Clinical trials require precise data management, ensuring accurate results and smooth study progression. TFS HealthScience supports pharmaceutical companies in this critical process.In this role as a Clinical Data Entry Specialist, you will be responsible for entering clinical data, anonymizing documents, and uploading them to designated platforms.About the...

We are looking for a clinical expert in dermatopathology and gastrointestinal pathology to join our team at a leading university hospital in southern Sweden.In this role, you will be responsible for providing expert diagnosis and treatment for patients, as well as contributing to ongoing academic work. Your key responsibilities will include:Case Reporting...

The successful candidate will have a strong understanding of international regulatory guidelines and standards such as FDA, CE Marking, NBOG, ISO 13485, MDR, etc., and will be able to apply this knowledge to prepare successful regulatory submissions.You will work closely with cross-functional teams to ensure compliance with global regulatory requirements and...

About BrainlabBrainlab is a software-driven medical technology company that develops, manufactures, and markets innovative solutions for patient treatments. Founded in 1989 in Munich, Germany, we have grown into a global organization with over 2400 dedicated team members worldwide.We are committed to improving patient outcomes through cutting-edge technology...

About the CompanyBrainlab is a global leader in software-driven medical technology, empowering healthcare professionals to deliver exceptional patient care. Our innovative solutions enable clinicians to provide more efficient, effective, and less-invasive treatments.We are committed to fostering a collaborative and inclusive work environment, where talented...

About TFS HealthScienceWe are a 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.The QPPV/Safety Manager is part of the Project Delivery...

About this RoleTFS HealthScience is a Contract Research Organization (CRO) that provides full service-capabilities, resourcing and functional service (FSP) solutions to biotechnology and pharmaceutical companies. We partner with our clients throughout their entire clinical development journey.The QPPV/Safety Manager is responsible for management of Drug...

Role OverviewTFS HealthScience is a leading global Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. We offer full service-capabilities, resourcing and functional service (FSP) solutions.The QPPV/Safety Manager plays a crucial role in the Project Delivery...

Are you an accomplished pathologist seeking a new challenge in a collaborative environment?A leading hospital in southern Sweden is recruiting skilled pathologists to join a dynamic team where expertise and innovation go hand-in-hand.About the PositionAs a pathologist, you will work closely with a forward-thinking team focusing on general pathology and...

Are you a pathologist looking to take your career to the next level?A leading hospital in southern Sweden is seeking skilled pathologists to join a highly specialized and collaborative environment where expertise and innovation go hand in hand.About the roleAs a pathologist, you will work within a dynamic and forward-thinking team, focusing on both general...

Job Overview:We are seeking a skilled Regulatory Affairs Specialist to join our regulatory team. In this role, you will be responsible for ensuring compliance with international regulatory standards and guidelines applicable in our active markets.Your key responsibilities will include:Preparing and submitting regulatory documentation required for the...

Responsibilities:As a Regulatory Affairs Specialist, you will be responsible for ensuring compliance with international regulatory standards and guidelines applicable in our active markets. Your key responsibilities will include:Preparing and submitting regulatory documentation required for the approval and registration of new and existing products in...

Key Responsibilities:The Regulatory Affairs Specialist will be responsible for ensuring compliance with international regulatory standards and guidelines applicable in our active markets. The key responsibilities of this position include:Preparing and submitting regulatory documentation required for the approval and registration of new and existing products...

Job Description:Magle Chemoswed is a leading provider of Contract Development and Manufacturing Organization (CDMO) services to the Life Science industry. We are seeking a highly skilled Regulatory Affairs Specialist to join our dynamic regulatory team.In this role, you will be responsible for ensuring compliance with international regulatory standards and...