Clinical Data Management Specialist

Role Summary:George Clinical is seeking a highly skilled Clinical Research Specialist to join our team. As a Clinical Research Specialist, you will provide medical and academic input to various aspects of George Clinical studies.Key Responsibilities:Provide medical and academic expertise for new and existing George Clinical studies.Support Endpoint...

Job DescriptionJob Title: Clinical Data SpecialistMUM Fortrea Development India Pvt Ltd is seeking a highly skilled Clinical Data Specialist to join our team.Responsibilities:Review clinical trial data in accordance with global data management plans and applicable standardized data management processes.Run ancillary programs to support data review...

Job Responsibilities:We are seeking a Clinical Data Specialist to perform medical data coding aspects of assigned projects with supervision. The successful candidate will work with the technical service group staff and aid in personal career development, interpersonal skills, and achievement of competency standards.The selected candidate will assist the...

Transform drug and device development for our global partners and patients. We are seeking a highly motivated Clinical Data Specialist to join our team.About FortreaAs a leading global contract research organization (CRO) with a passion for scientific rigor, we provide pharmaceutical, biotechnology, and medical device customers a wide range of clinical...

Job SummaryWe are seeking a Clinical Data Specialist to join our team at MUM Fortrea Development India Pvt Ltd. As a Data Management Specialist, you will be responsible for ensuring the quality and integrity of clinical trial data.Main ResponsibilitiesEnsure all allocated projects are carried out in accordance with relevant protocols, SOPs, and GCP...

Job SummaryWe are seeking an experienced Clinical Data Specialist to join our team at MUM Fortrea Development India Pvt Ltd. The successful candidate will be responsible for managing clinical trial data, ensuring accuracy and quality, and collaborating with project teams to deliver high-quality results.About the RoleThe Clinical Data Specialist will work...

At Integra Connect, we are seeking a highly skilled Clinical Data Standards Specialist to join our team in Bangalore.The estimated salary for this position is ₹1,200,000 per annum, based on industry standards and location.The successful candidate will have the opportunity to work on groundbreaking projects involving real-world data, collaborating with an...

About the RoleThe Senior Medical Reviewer will be responsible for conducting comprehensive medical reviews of clinical trial data across various therapy areas within the drug development portfolio. This role ensures the highest quality and consistency of medical data, with a strong emphasis on patient safety, protocol adherence, and compliance with Good...

About ACL DigitalWe are a leading provider of innovative solutions for clinical trials.Job Title: Clinical Data Coordinator SpecialistLocation: Bangalore / Hyderabad / ChennaiJob Type: Full-timeEstimated Salary: ₹ 8,00,000 - ₹ 12,00,000 per annumAbout the RoleWe are seeking an experienced Clinical Data Coordinator Specialist to join our team. The...

We are seeking a skilled Clinical Data Management Specialist to join our team at Lilly. As a key member of our Clinical Data Management team, you will play a crucial role in ensuring the quality and integrity of clinical data for our trials.Key Responsibilities:Execute Lilly business requirements for study/program vendors to deliver clinical trial...

Job Title: Clinical Data SpecialistLocation: Bengaluru, Karnataka, India (Remote)Contract Type: Full-timeSeniority Level: Mid-Senior levelWe are seeking a skilled Clinical Data Specialist to join our team at Fortrea, a leading global contract research organization. With a passion for scientific rigor and decades of clinical development experience, we provide...

At MUM Fortrea Development India Pvt Ltd, we are seeking a highly skilled Senior Clinical Data Specialist to join our team of professionals.Job Summary:The successful candidate will be responsible for the clinical medical data coding aspects of assigned projects, working closely with the technical service group staff and assisting in personal career...

Job Title: Clinical Data Manager - Medical Insights SpecialistWe are seeking a highly skilled Clinical Data Manager to join our team at IQVIA. As a Clinical Data Manager, you will be responsible for ensuring the accuracy and integrity of clinical data, providing medical and scientific expertise to drive data quality and integrity, and collaborating with...

OverviewBAN Fortrea Clinical Development Pvt Ltd is a leading clinical development company seeking a highly motivated and detail-oriented Regulatory Compliance Specialist to join our team. The ideal candidate will have a strong understanding of regulatory legislation, guidance, and practice in the assigned countries.

About the RoleFortrea Development India Pvt Ltd is seeking a highly skilled Clinical Data Specialist I to join our team. In this role, you will be responsible for performing clinical medical data coding aspects of assigned projects with supervision. You will work closely with the Coding team and Lead Data Reviewer on all coding aspects for project(s)...

As a leading global contract research organization with a passion for scientific rigor, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across multiple therapeutic areas.Key Responsibilities:• Perform clinical medical data coding aspects of assigned...

Company Overview:MS Clinical Research is a pioneering organization in the field of neuroscience, dedicated to advancing knowledge and improving patient care. Our team is passionate about delivering high-quality research studies that push the boundaries of human understanding.Salary:$85,000 - $110,000 per annumJob Description:We are seeking an experienced...

Clinical Regulatory Document Specialist Role SummaryThis highly skilled Clinical Regulatory Document Specialist is responsible for crafting and reviewing complex clinical trial documents, ensuring they accurately reflect associated data and adhere to Global pharma company standards and global, regional, and/or local regulatory requirements. The ideal...

We are seeking a highly skilled Medical Laboratory Support Specialist to join our team at MS Clinical Research. In this role, you will play a vital part in supporting the laboratory operations and ensuring the delivery of high-quality results.About the RoleAs a Medical Laboratory Support Specialist, your responsibilities will include:Supporting laboratory...

Job SummaryThe Clinical Collaboration Specialist will play a key role in initiating and managing clinical and research collaborations at hospitals, medical centers, and academic institutions globally and regionally. This position will work closely with internal and external stakeholders, including Clinical and Regulatory Affairs, Innovations, Product...