Clinical Application Specialist

About NoccarcNoccarc is a pioneering medical device company that designs and manufactures innovative Smart Medical Devices and an integrated Digital Platform for ICUs. Our cutting-edge products adhere to international standards, such as US-FDA and CE guidelines, and are highly competitive in the global market.With a strong focus on research and development,...

About NoccarcNoccarc is a pioneering medical device company that specializes in designing and manufacturing innovative Smart Medical Devices and an integrated Digital Platform for ICUs. Our cutting-edge products adhere to international standards, such as US-FDA and CE guidelines, and are highly competitive in the global market.With a strong focus on research...

Job Title: Clinical Safety SpecialistJob Summary:We are seeking a highly motivated Clinical Safety Specialist to join our team at Lifelancer. As a Clinical Safety Specialist, you will be responsible for implementing and promoting the use of consistent, efficient, and quality processes to meet timelines and deliverables according to requirements and standard...

Job SummaryAs a Clinical Safety Specialist at Lifelancer, you will be responsible for implementing and promoting the use of consistent, efficient, and quality processes to meet timelines and deliverables according to requirements and standard operating procedures. You will assume accountability for the deliverables and ensure compliance of operations with...

Job DescriptionThe Clinical Trials Specialist should have a Life science / bio medical background graduate or have other healthcare related degree qualification (chemistry, biology, biotechnology, veterinary science etc.) This is an opportunity for new graduates to start and develop their career within drug safety.As a Clinical Trials Specialist, you will...

About the RoleWe are seeking a highly detail-oriented and organized Clinical Document Specialist I to join our team at TransPerfect. As a Clinical Document Specialist I, you will play a critical role in reviewing and managing essential and non-essential TMF documents for assigned projects.Key ResponsibilitiesReview documents in eTMF workflow to complete...

Key ResponsibilitiesAs a Clinical Development Specialist at CSS Fortrea Scientific Pvt Ltd, you will be responsible for implementing and promoting consistent, efficient, and quality processes to meet timelines and deliverables according to requirements and standard operating procedures. You will assume accountability for the deliverables and ensure...

About Innovaderm ResearchInnovaderm Research is a renowned contract research organization (CRO) specializing in dermatology. With over two decades of experience, our organization has established a solid reputation for delivering high-quality research and services that exceed client expectations.Job Title: Clinical Study Design SpecialistWe are seeking a...

Key Responsibilities:As a Clinical Research Specialist at Lifelancer, you will be responsible for implementing and promoting the use of consistent, efficient, and quality processes to meet timelines and deliverables according to requirements and standard operating procedures.Responsibilities:Ensure compliance of operations with governing regulatory...

Explore a career in clinical document management with TransPerfect. As a Clinical Document Specialist I, you will be responsible for reviewing essential TMF documents and ensuring they are accurately filed in the eTMF. Key responsibilities include reviewing documents in eTMF workflow, sustaining quality thresholds, and meeting daily productivity goals....

We are seeking a highly skilled Clinical Operations Specialist to join our team at 2coms. As a Field Clinical Coordinator, you will play a crucial role in transforming healthcare in India with our cutting-edge Connected Healthcare technology.Key Responsibilities:Visit hospitals to set up devices and conduct site recce.Train nurses, doctors, and patients on...

Make a Difference in the Pharmaceutical SectorWe are seeking a skilled Pharma Talent Acquisition Specialist to partner with clients and understand their recruitment needs.Key Responsibilities:Source and engage top talent in the pharma and biotech industries.Manage the full recruitment cycle from sourcing to placement.Requirements:Proven experience supporting...

Make a Difference in the Pharmaceutical SectorWe are seeking a skilled Pharma Talent Acquisition Specialist to partner with clients and source top talent in the pharma and biotech industries.Key Responsibilities:Partner with clients to understand their recruitment needs.Source and engage top talent in the pharma and biotech industries.Manage the full...

Job Title: AI Lead - Clinical Data SpecialistJob Summary:We are seeking an experienced AI Lead to join our team at Saama, where you will play a pivotal role in developing innovative solutions that leverage cutting-edge Large Language Models (LLMs) to revolutionize clinical business decision-making.Key Responsibilities:Design and implement advanced Generative...

About the RoleWe are seeking a highly skilled Clinical Document Specialist II to join our team. As a key member of our Clinical Operations group, you will be responsible for ensuring the quality and accuracy of clinical documents in our electronic Trial Master File (eTMF).Key Responsibilities:Review and finalize the indexing of documents in the eTMF...

Key Responsibilities:As a Clinical Safety Specialist at Lifelancer, you will be responsible for implementing and promoting the use of consistent, efficient, and quality processes to meet timelines and deliverables according to requirements and standard operating procedures. You will assume accountability for the deliverables and ensure compliance of...

ResponsibilitiesThe eClinical Systems Analyst will support clients in the development, maintenance, and closeout of clinical trials. This includes the use of various eClinical systems, such as electronic Trial Master File (eTMF), Study Start up (SSU), and Clinical Trial Management System (CTMS). The successful candidate will have experience with eClinical...

As a leading global contract research organization, Fortrea is seeking a skilled Clinical Trials Medical Specialist to join our team. In this role, you will be responsible for undertaking primary medical review of cases, including medical assessment of the case for seriousness, listedness/labeling, causality, adverse event coding and narrative review.Key...

We are seeking a skilled Business Operations Specialist to join our team at GiGa-Ops Global Solutions. The ideal candidate will have a strong background in data analysis and excellent SQL skills, with a willingness to learn ETL and data visualization tools. This role is critical in bridging the gap between business needs and technical solutions, ensuring the...

Job Description for Medical Writer at Clini Launch Research InstituteWe are seeking a skilled Medical Writer to join our team at Clini Launch Research Institute. The ideal candidate will have a strong background in clinical research and experience in writing high-quality documents for regulatory submissions.Preparation of Clinical Trial ProtocolsPreparation...