Data Entry Specialist for Clinical Trials

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...

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...

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,...

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...

Role DetailsThis is a full-time position as a Clinical Data Entry Specialist with TFS HealthScience.The role involves working on a high-impact clinical study, 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...

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 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...

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...

Company OverviewAt Brainlab Ltd., we pioneer software-driven medical technology that transforms treatment and patient care. Our innovative solutions in the field of oncology enable clinical personnel to deliver faster and more precise treatments, ensuring better health outcomes for patients worldwide.

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...

Magle Group is growing and we are looking Regulatory Affairs Specialist who is looking for a new challenge and who wants to be part of a small but dynamic regulatory team. Magle Group is supporting other Life Science Companies by providing CDMO services as well developing and manufacturing our own products with DSM technology. This role will focus on...

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...

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...

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...

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