...Clinical Research Associate Template
We are looking for an organized, flexible clinical research associate to oversee clinical trials. The clinical research associate will develop and outline trial protocols, establish trial sites, train site staff, and manage Investigational...
...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
Clinical CTC-1
Remote job
...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...
...visual resemblance of a scholar rock to protein structures, the clinical-stage company is focused on advancing innovative treatments where... ...and on LinkedIn.
Summary of Position:
The Senior Clinical Trial Manager is responsible for all operational aspects of a clinical...
...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...
About the job
Job Description Senior Business Analyst
Required Skills:
5+ years of experience with minimal 4-year experience in Client Management and Business/System Analysis Role.
At least 3 year of experience in HealthCare or Pharmaceutical (CRO) industry.
...
...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...
...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...
Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company focused... ...is seeking a highly motivated Medical Director or Senior Medical Director with significant... ...medical lead for CAR T-cell therapy clinical trials in multiple autoimmune disease...
...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 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...
...Amity University Uttar Pradesh, Noida invites applications for Director- Amity Institute of Behavioural (Health) & Allied Sciences (AIBHAS... ...with Rehabilitation Council of India (RCI)
M.Phil in Clinical Psychology
Ph.D. degree in Clinical Psychology or relevant field...
Amity University
Noida
3 days ago
Summary
The Operational Excellence Director, Clinical Development will provide strategic planning and operational execution support to the Head of Operational Excellence, Clinical Development to deliver on the CD Operational excellence goals aligned with the overall CD strategy...
...(“EPM”), identifies patients with disease risk and streamlines clinical decision analysis so clinicians can work at the top of their licenses... ...motivated and experienced individual to join our team as a Director of Clinical Programs. In this role, you will be responsible for...
...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...
...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...
Hi, we're Oscar. We're hiring a Senior Medical Director to join our Clinical Care Team
Oscar is the first health insurance company built around a full stack technology platform and a focus on serving our members. We started Oscar in 2012 to create the kind of health insurance...
...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...
...Department – Clinical Medical Regulatory (CMR)
Do you want to be a part of a high performing team in Novo Nordisk that plays a critical... ...to them progress and critical issues that may impair trial progress. In some cases, the CRA may have direct contact with the...
About the job
Basic understanding of the principles of investigator grant template drafting
Capable of reviewing and analyzing a protocol schedule of events to draft applicable budget grid and payment schedules therefrom
Basic understanding of the pharmaceutical product...
Summary
Drive and execute labelling activities for clinical trial supplies (IMP) to ensure fulfillment of supply chain. Resulting in no stock outs /missed milestones and/or supply interruptions impacting patients due to label quality or availability.
Has operational end-to...
Summary
“150! Clinical scientific experts, globally, are part of Global Drug Development (GDD) team, working to ensure clinical trial data and regulatory reports are of highest quality throughout the life cycle of each program, across all disease areas. Be part of a dedicated...
...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...
...As a Clinical Research Associate, you'll play a pivotal role in ensuring the successful execution of clinical trials. From monitoring trial progress to ensuring regulatory compliance and participant safety, you'll be at the forefront of cutting-edge medical research.
Key...
...Clinical Data Management We are looking for a detail-oriented and organized Clinical Data Manager (CDM) to join our expanding clinical research... ...integrity, ensuring the smooth and efficient flow of clinical trial data from collection to analysis. You will play a pivotal role in...
One of Upwork's largest clients, a fortune 500 technology company , is in search of a self-driven, engaging English speaking M365 Technical advisor consultant with knowledge of M365 products.
Job Description
Candidates will be responsible for responding to...
...Job Title : Clinic Receptionist
Responsibilities:
Serves patients by greeting and helping them, scheduling appointments, and maintaining records and accounts.
Welcomes patients and visitors in person or on the telephone, and answering or referring inquiries.
Optimizes...
...within a young, ambitious health company on the path to becoming the clinical research leader in Europe thanks to our 900 Excelyates. Our... ...practices and associated documentation
Experience in clinical trial databases and applications, clinical data flow, data review, and...
Summary
-Contributes, with appropriate oversight, to all aspects of global clinical trial(s) to deliver study outcomes within schedule, budget, quality/compliance and performance standards. May lead specific aspects of global clinical trial(s). Core member of the Clinical...