THE LARGEST COLLECTION OF JOBS ON EARTH
Supports PDF, DOC, DOCX, TXT, XLS, WPD, HTM, HTML files up to 5 MB
Medical Data Entry Specialist We have a client seeking a Medical Data Entry Specialist. The Medical Data Entry Specialist is responsible for entering information into the various clinical systems used by ..
Role : Scrum MasterLocation : BangaloreDivision : SHS TE DC IND DI-SY DEV1Mode of employment: Full timeResponsibilities•tAs a Scrum Master, manage one or more Scrum Teams, ensuring timely delivery of features ..
Role: Engineer – Quality ManagementExperience: 3-6yrsQualification: B.E\B TechJob description:• Good knowledge of the quality management systems fornmedical device manufacturers (ISO 9001:2015,ISO 13485:2016,21CFR820 etc.)n• Ensuring compliance of products with legal and normative ..
Healthcare Consultant We are Healthcare consultant and working on different hospitals and education training projects in India, Africa, Nepal etc. Skills: Compliance and Safety Training , Audit , Value Based Healthcare ..
Preparation of documents and facilitation of documentation management in R&D while following established guidelines for correctness, completeness and clarity.Preparation of documents such as Manufacturing Batch Records, Study Protocol and Reports, Stability ..
... software. Define/ Author Security and compliance requirements for the system in ... and regulatory colleagues to ensure compliance Participate/Lead risk assessments and develop ... security, especially as applicable to..
Clinical Data Associate III Come discover what our 25,000 employees already know: work here matters everywhere. We're a growing and evolving biopharmaceutical industry leader, which means you'll have endless opportunities to ..
Description Position at Wind River ABOUT WIND RIVER Wind River is a global leader in delivering software for mission-critical intelligent systems. For more than four decades, the company has been an ..
Job Title: Clinical Compliance Coordinator with US healthcare experience Location: Chennai Job Details: ... position is maintaining all relevant compliance documentation for candidates on assignment ... Recruiters in order to..
Ensure smooth functioning of the hospital by providing quality medical and nursing careFormulating policies and proceduresAbiding statutory compliance and handling medico legal casesFormation of new specialties and attract promising cliniciansLiaison between ..
7 years' experienceExperience in Quality management system.Good understanding of Regulatory Guidelines, Good documentation practices and Good manufacturing practices.Knowledge of current Good Manufacturing Practices and the applicable GxP regulations and standards.Proactive approach ..
At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science.In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and ..
Job OverviewProvide Trial Master File (TMF) related assistance to study teams. Ensure all work is conducted in accordance with Standard Operating Procedures (SOPs), policies, practices, good clinical practices, applicable regulatory requirements, ..
Job OverviewApply knowledge and expertise for Safety Aggregate Report and Analytics (SARA) Center deliverables including safety aggregate reports, literature surveillance, signal management activities and benefit risk management documents.Essential Functionsu2022 Serve as ..
•tQuality Culture:-tEnsure awareness for quality focus to increase customer satisfaction, particularly in the development process-tPlan, implement and live Quality culture within Product Line and organization level (Implement the defined processes, improve ..