clinical study report

Clinical Study Manager (AI Training) About The Role What if your clinical trial expertise could directly shape how AI understands and communicates the science of medicine? We're looking for experienced Clinical Study Managers to support the operational execution of clinical research projects — ensuring studies run on time, within budget, and to the...

Job Tittle - Clinical Study Budget SupportLocation - HyderabadAbout the job:Join the Clinical Study Support and Operations (CSSO) team, where you will play a vital role in supporting clinical study operations while ensuring compliance with global standards and regulations. In support of the Clinical Supply Chain Operations (CSCO) team, who is responsible for...

Clinical Study Manager (AI Training) About The Role What if your clinical trial management expertise could directly shape how AI understands and advances healthcare research? We're looking for experienced Clinical Study Managers to oversee the operational execution of clinical trials — ensuring studies run on time, on budget, and to the highest quality...

Clinical Study Manager (AI Training) About The Role What if your clinical trial management expertise could directly shape how AI understands and reasons about real-world healthcare research? We're looking for experienced Clinical Study Managers to oversee the operational execution of clinical trials — and help ensure the AI systems being trained on this...

Job description Role & responsibilities To take care of emergency medical management To ensure Volunteer well-being To ensure proper co-ordination and conduct of the bio study To ensure proper functioning and maintenance of instruments To monitor documentation / records and storage To review employee health check-up reports and promote preventive healthcare...

Build our future togetherRegeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to...

Clinical Study Manager IIAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that...

Exciting Opportunity in India!   Clinical Data Report Programmer Minimum Requirements: Bachelor's degree (or equivalent education) in Life Sciences, Computer Science, Statistics, Biostatistics, Data Science, Health Sciences, or a related field. Experience: Minimum of 5–7 years' experience in Clinical Data Management report programming within the...

Job Summary The Clinical Operations Manager will lead and oversee end-to-end clinical study execution across Skin, Hair, and Oral domains. This role is responsible for managing study operations, ensuring compliance with protocols, SOPs, and regulatory guidelines, and coordinating with internal teams, investigators, and sponsors. The candidate will ensure...

Detail-oriented Clinical Research Coordinator (CRC) with 3+ years of experience supporting Phase I-IV clinical trials across Oncology, Cardiovascular, Infectious Disease, and Pharmaceutical therapeutic areas. Proficient in ICH-GCP E6(R2/R3) guidelines, IRB submissions, eConsent, and regulatory document management. Skilled in Decentralized Clinical Trials...

Career CategorySupply ChainJob DescriptionRole DescriptionLet’s do this. Let’s change the world. In this vital role, you will serve as lynchpin between Global Study Planners and internal and external customers to ensure supply for our important patients participating in Amgen’s global clinical trials. Along with local team members, you support the...

Role Overview An entry-level Clinical Research Associate (CRA) to monitor clinical trial sites, verify data quality and ensure GCP compliance and patient safety across assigned studies. Key Responsibilities ■ Support and conduct site visits for study initiation, monitoring and close-out ■ Verify source documents against Case Report Forms (CRFs) for...

Career CategoryClinical DevelopmentJob DescriptionHOW MIGHT YOU DEFY IMAGINATION?If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission -to serve patients - drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together -...

Career CategoryOperationsJob DescriptionRole Name: Study Delivery Associate  ABOUT AMGEN Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen...

Company DescriptionEurofins Advinus is a premier preclinical and early development CRO offering drug discovery, preclinical and development stage contract research services in the areas of discovery services, regulatory Toxicology (Safety Assessment), DMPK, Analytical R&D Services and API CDMO. Eurofins Advinus manufactures drug substances to support...

Company DescriptionENGLISHEurofins Scientific is an international life sciences company, which provides a unique range of analytical testing services to clients across multiple industries. The Group believes it is the world leader in food, environment, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global...

Job description Role & responsibilities . Feasibility assessment/ new product evaluation • Literature review and BA/BE study designing • BE Study Monitoring • Preparation of documents for regulatory submission (i.e BENOC, Import license application etc.) • Establishment and maintenance of study documents • Document preparation for dossier...

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Global Study Lead (FSP) based in India. This is a senior clinical operations leadership role responsible for the global delivery of complex clinical studies.You’ll provide end-to-end operational leadership, from study...

Position Title Study Counsellor Location Gorakhpur, Pune, Satara Organisation YR Gaitonde Medical Educational & Research Foundation (YRGMERF) Experience Required 3–5 years Compensation Remuneration will reflect the candidate’s experience and skills, subject to the approved budget   About YRG...

Summary of Responsibilities:Draft, review, negotiate, and finalize Clinical Trial Agreements (CTAs), confidentiality agreements, amendments, and related site contract documentation.Coordinate with sponsors, legal teams, clinical operations, and study teams to facilitate timely contract execution.Manage site agreement timelines and ensure contracts are...