SAS/PH- Clinical trial analysis

Clinical trials are the actual experimental studies in which human volunteers are included, after their consent, to test new treatments, instruments,Read More

ICON plc is a leading healthcare intelligence and clinical research company. We take pride in creating a diverse and innovative work environment, and we invite you to be part of our journey to influence the future of clinical development.Clinical Trial AssistantLocation : Mumbai, On-siteResponsibilities:- Document collection and submission support- Vendor...

Clinical Trial Associate Mumbai or Vadadora, India (hybrid: 3 days office, 2 days home) Salary: Competitive + Benefits + Bonus If you are an agile, committed, and innovative clinical trial professional then we want to hear from you Join us to help improve peoples' lives and make healthcare better for everyone Why Pharmanovia? Pharmanovia is...

We are looking for a skilled Clinical Trial Medical Writer!Experience: 3+ years working in the field of clinical trial medical writingDevelop case report formats, protocol letters, and record forms crucial for clinical trialsPrepare all required documentation for the initiation, execution, and completion of clinical trialsConduct literature reviews and...

Mumbai or Vadodara, India (hybrid: 3 days office, 2 days home):Salary:Competitive + Benefits + Bonus:If you are an agile, committed, and innovative clinical trial professional, then we want to hear from youJoin us to help improve peoples' lives and make healthcare better for everyoneWhy Pharmanovia?:Pharmanovia is a dynamic, fast-growing international...

ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. Clinical Trial Assistant Location : Mumbai, Office based Responsibilities: What you will be...

Provides comprehensive programming leadership and support to development teamsEnsures quality of deliverables by consistently applying analysis and reporting standards and driving compliance with regulatory requirements, corporate and departmental SOPs, and work practicesDrives the development and implementation of innovative strategies and technologies for...

Clinical Programming: Clinical Programming Lead (SDTM Programming)At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are working to create a world without disease and the development of best-in-industry data science capabilities is critical to our ambition to be most innovative healthcare company.Within Integrated Data Analytics & Reporting...

Essential Job Duties:1) Document and track study activities using relevant forms and tools, as well as relevant Project Management Systems with guidance/support2) Assist in the preparation of study and site specific materials in accordance with relevant SOPs3) Complete minute taking and documentation for sponsor/external or internal teleconferences as...

As a leading contract research organization (CRO), Labcorp Drug Development provides comprehensive drug development solutions for a range of industries. Our services cover the preclinical, clinical and post-market phases of drug development, the product life cycles for medical device and diagnostics and development services paired with regulatory support for...

Department: Clinical Development CentreDo you want to be a part of a high performing team in Novo Nordisk that plays a critical role in driving the success of the business? Do you have what it takes: the right drive, a sharp mind, customer orientation, openness and focus on what matters and a genuine interest in working with people? If you find challenges...

Overview:As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements, and industry standards throughout the trial processResponsibilities:1 Trial...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

About the company and the position:Hey there! Are you a Clinical Research Associate (CRA) looking for an exciting opportunity to be a key player in clinical trials? Well, look no further! Join our team and be a crucial part of the development and execution of cutting-edge clinical research. Here's what you'll be doing:Responsibilities: Assist in developing...

About the job At Cytel, we work hard to create successful careers with significant professional growth for our employees, as a result of which they work hard to make Cytel successful. Cytel is a place where talent, experience and integrity come together to advance the state of clinical development. Senior Clinical Programmer (Quality/Technical Review) role...

We are Growing Let us support your career journey the Biorasi way. Innovative, Collaborative, Dynamic and Evolving. Capitalizing on your strengths while encouraging work-life balance. Biorasi is an award-winning, customer-focused, full-service clinical research organization, and we are unlike any CRO you've ever heard of.Biorasi is looking for top performers...

The Sr. Clinical Project Manager is responsible for managing Clinical Operations activities and providing functional supervision for Clinical Operations staff within their assigned Clinical Development Plan (CDP) as determined by the Director of Clinical Operations. The CPD conducts required tasks in collaboration with Clinical Project Management, Clinical...

The Sr.Clinical Project Manager is responsible for managing Clinical Operations activities and providing functional supervision for Clinical Operations staff within their assigned Clinical Development Plan (CDP) as determined by the Director of Clinical Operations.The CPD conducts required tasks in collaboration with Clinical Project Management, Clinical...

Job Profile: Senior Statistical ProgrammerEducation Requirements: Bachelor's degree from reputable university preferably in science/ mathematics related fields Attained SAS certificationTechnical Skills Requirements: Must have excellent knowledge of SAS Base, and good knowledge of SAS graph and SAS Macros. Capable of programming simple statistical procedures...

About thejobAt Cytel we work hard tocreate successful careers with significant professional growth forour employees as a result of which they work hard to make Cytelsuccessful. Cytel is a place where talent experience and integritycome together to advance the state of clinicaldevelopment.Senior Clinical Programmer(Quality/Technical Review) role is...