Search Results: 3,801 vacancies
Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company focused on developing cell therapies for patients suffering... ...how autoimmune diseases are treated
The Senior Clinical Trials Manager will be a key member of the Clinical Operations team, leading...
...Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and... ...other activity or lack thereof which may jeopardise the clinical trial delivery or patient safety .
• *Ensure all necessary trainings...
...to ensure that people living with a chronic disease can live a full life. We are looking for a dedicated EU Submission Lead for Clinical Trials to join our Global Regulatory Affairs team.
If you are passionate about driving change and navigating complex agendas, apply today...
...Lead the development of the study specific eTMF plans for assigned clinical studies.
Perform quality control of documents submitted to the... ...using the established acceptable criteria
Ensure clinical trial documentation is consistent with eTMF specifications, ICH-GCP guidelines...
...Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and... ...and you’ll be helping shape an industry. The role: The Clinical Trial Manager is responsible for the delivery of all clinical aspects...
Remote job
...Job Summary:
The Manager of Clinical Trials will lead and oversee all clinical trial activities for our medical device portfolio, ensuring compliance with international regulatory standards for markets including the U.S. and Japan. The role requires extensive experience...
...Sun is seeking a Global Trial Manager, Clinical operations within its clinical development Team in India. The Global Trial Manager, Clinical Operations will report into Global Trial leader, Clinical Operations. Under the direction of the Global Trial leader, Clinical Operations...
...Clinical Data Management (CDM)
Clinical Data Managers (CDMs) are responsible for ensuring the accuracy, integrity, and completeness of data collected in clinical trials. They work closely with clinical investigators, statisticians, and other members of the clinical trial...
...lock with the oversight of the LCTL/CTL, as assigned. Support the clinical protocol development process in collaboration with the CTL/Lead... ...protocols, amendments and related documents; drive and/or supprt trial-related documents and processes.
development of clinical section...
...TMF Specialist Responsibilities:
Receive and process clinical trial documents, ensuring proper filing and indexing.
Perform quality checks on documents to ensure they meet regulatory requirements and study protocols.
Maintain and update the TMF according to established...
...Clinical Trial Foundations (CTF), as part of Clinical Design, Delivery and Analytics (CDDA), delivers innovative and reliable systems, processes, and information to enable clinical development and speed medicines to patients. The Clinical Systems Management role will support...
Rs 1 - 2 lakhs p.a.
...Post: Lab Technician
Location: Khar Road
Salary: 10K - 12K
Experience: Fresher and Experience Both apply
Job Description:
Perform a wide range of laboratory tests and experiments following standard procedures and protocols.
Prepare and maintain accurate records...
...Post : Clinical Research Associate/Clinical Trial
Location : Ahmedabad-(Science City Road, Sola)
Exp : 3Yrs to 8Yrs
Roles & Responsibilities:
- Perform on-site in-process and retrospective monitoring visit of clinical phase of the clinical trials, PK and BA/BE studies...
Rs 5 - 6 lakhs p.a.
...Regulatory requirements, In-house SOPs and SSPs.
· Conduct audit of Clinical Data Management, Biostat and Programming, Consumer Research, and... ...).
· Maintain, Track and Distribute SOPs and forms
Clinical trial,Data Management
Designation: QA Auditor - Clinical Trials...
...Department – Clinical Medical Regulatory (CMR)
Do you want to be a part of a high performing team in Novo Nordisk that plays a critical... ...working environment, you may be our new Project Manager (CDC Trial Manager) for the Clinical Medical Regulatory team based at Mumbai...
...communicable diseases and injury.
With offices in Australia, China, India and the UK, our 700+ people support 245+ active projects and clinical trials across 50+ countries, with 400+ more staff across our social enterprises. We focus on the global health challenges that cause the...
...difference in the healthcare industry? We are looking for a skilled Clinical Programming Specialist to join our Data Management Operations and... ...and processes that may arise in the course of a clinical trial. Create and execute reports within the clinical reporting systems...
...Clinical SAS We are looking for a highly skilled and experienced Clinical SAS Programmer to join our growing team. The ideal candidate will have a strong understanding of SAS programming, clinical trial data, and statistical analysis methods. The Clinical SAS Programmer will...
...new data collection requirements in assigned studies and provide clinical input into the development of new and updated clinical Data... ...as well as 3rd party data collection methodologies) for assigned trials/therapy areas as needed.
Provide timely information for and support...
...Responsibilities
Support CRAs with the setup monitoring and closeout of clinical trials in accordance with Good Clinical Practice (GCP) ICH guidelines and company SOPs.
Assist in site qualification initiation and monitoring visits.
Review and track clinical trial...
