Search Results: 7,321 vacancies
...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...
...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...
...ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving... ...to shape the future of clinical development.
Clinical Trial Assistant
Location : Mumbai, Office based
Responsibilities...
...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...
...Job Title: Clinical Trials Data Strategist - AI
Location: Remote
Job Type: Full-Time
About Us:
At ngram, we are at the forefront of revolutionizing the clinical trial industry by integrating advanced artificial intelligence technologies into our solutions. Our...
...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.
...
...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...
...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...
...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
1 day ago
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...
...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...
Summary
To lead a community of ~ 20 Clinical Data Acquisition Specialists, Clinical Data Scientists and Coding Specialists as assigned to... ...and able to take the right decisions to solve issues at the trial/program delivery level.
•Understands Health Authority requirements...
...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...
...(“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...
...Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential...
...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...
...Job Description
JOB TITLE : Associate Director- Clinical Regulatory Writing
CAREER LEVEL: E
Lead the way for a new breed of solutions-oriented Regulators
Champion a new approach to Regulatory that supports quick decision-making and balanced risk-taking. Curious...
...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...
...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...
