Clinical Development Specialist

Clinical Document Specialist IAre you passionate about clinical research and looking to expand your skills in TMF management? Do you want to work with a team that nurtures talent and provides growth opportunities? If so, we have an exciting opportunity for a Clinical Document Specialist I at TransPerfect.About the Role:As a Clinical Document Specialist I,...

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 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...

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...

About the RoleWe are seeking a highly skilled Clinical Document Specialist II to join our team at TransPerfect. As a Clinical Document Specialist II, you will play a critical role in ensuring the quality and accuracy of indexed documents in the eTMF.Key Responsibilities:Review and finalize the indexing of documents in the workflow to ensure accuracy and...

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...

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...

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...

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...

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...

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,...

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...

About NoccarcNoccarc is a leading designer and manufacturer of Smart Medical Devices and an integrated Digital Platform for ICUs, revolutionizing ICU operations and management.Our products adhere to international standards such as US-FDA and CE guidelines, competing strongly with top international products.With over 9 patents, our dynamic in-house R&D team...

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...

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...

Job Title: AI Lead - Clinical Data SpecialistJob Description:At Saama, we're at the forefront of transforming business through advanced AI technologies. As an AI Engineer specializing in Generative AI applications for clinical data, you'll play a pivotal role in developing innovative solutions that leverage cutting-edge Large Language Models (LLMs) to...

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...

Job Title: eClinical Systems AnalystThe eClinical Systems Analyst plays a crucial role in supporting the development, maintenance, and closeout of clinical trials. This position requires a strong understanding of clinical trial processes and associated systems, particularly Trial Master File (TMF) processes.Key Responsibilities:Collaborate with Study Owners...

Job Title: Clinical Study Database DeveloperJoin IQVIA as a Clinical Study Database Developer and contribute to the success of our clients in the pharmaceutical industry.About the Role:We are seeking a skilled Clinical Study Database Developer to join our team. As a Clinical Study Database Developer, you will be responsible for building and maintaining...

Company OverviewPharmabharat is a Contract Research Organization (CRO) dedicated to assisting in clinical trials, with its headquarters located in India. Operating within the healthcare industry, Pharmabharat is a small enterprise employing between 11 to 50 professionals.Job OverviewWe are seeking a Clinical Research Associate for our operations based in...