Search Results: 16,860 vacancies
...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...
...Description
Join our international team and be the key support to clinical research projects, streamlining communication within a clinical... ...will:
Assist clinical project teams with selective aspects of trial management from start-up to close-out on a country level....
...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...
...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...
...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...
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.
...
...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 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...
...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...
.... Our commitment to innovation and patient satisfaction sets us apart and were looking for a passionate and driven Field Sales Clinical Consultant Orthodontist to join our team.
Job Description:
As a Field Sales Clinical Consultant Orthodontist at Snazzy Aligner youll...
...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...
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical... ...data collection to analysis
•Provides internal and external consulting services on topics related to CDISC standards compliance and standards...
Remote job
...Job Description
Department – Clinical Medical Regulatory (CMR)
Do you want to be a part of a high performing team in Novo Nordisk... ...inspiring working environment, you may be our new Project Manager (CDC Trial Manager) for the Clinical Medical Regulatory team based at Mumbai...
...If you’d like to be a part of Disability Leave Services (DLS) Clinical team to provide your clinical expertise for leave of absence, disability... ...looking for highly motivated individuals to work as Clinical Consultants for our Disability and Leave Service (DLS) organization. The “...
...Job Description
Department – Clinical Medical Regulatory (CMR)
Do you want to be a part of a high performing team in Novo Nordisk... ...communicates to them progress and critical issues that may impair trial progress. In some cases, the CRA may have direct contact with the...
...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...
...requirements in assigned studies and provide clinical input into the development of new and... ...data collection methodologies) for assigned trials/therapy areas as needed.
Provide... ...Conduct regular Clinical Data Reviews (CDR) in consultation with the Clinical Data Analyst and...
...cosmeceuticals, and personal care, NovoBliss Research conducts trials in diverse industries including Nutraceuticals, Dietary Supplements... ..., post-marketing observational studies, epidemiological clinical studies, and prospective interventional clinical studies, ensuring...
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...
