Search Results: 13,183 vacancies
...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...
...Department – Clinical Trial Administration
Are you looking for a challenging role in the pharmaceutical industry? Do you have experience in clinical trial administration? We are seeking a Clinical Trial Administrator to join our team in Bangalore. If you are detail-oriented...
...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...
...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...
...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...
...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...
...TMF Specialist Responsibilities:
Receive and process clinical trial documents, ensuring proper filing and indexing.
Perform quality... ...Collaborate with cross-functional teams, including clinical research associates, data managers, and regulatory affairs specialists.
Stay up...
...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.
...
...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...
...Clinical Trial Foundations (CTF), as part of Clinical Design, Delivery and Analytics (CDDA), delivers innovative and reliable systems, processes... ...of new releases and patches by providing technical expertise, associated training, and business process development.
• Resolve system...
...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...
...We are seeking a highly motivated and detail-oriented Clinical Research Associate Intern to join our team. This internship provides a hands-on learning experience within the dynamic field of clinical trials. You will gain exposure to the essential processes involved in conducting...
...Job Title : Clinical Research Associate (CRA)
Company : MS Clinical Research Pvt Ltd
About Us :
MS Clinical Research (MSCR) is a leading... .... We are committed to conducting high-quality clinical trials and contributing to the development of innovative medical solutions...
...Clinical Research Associate
Responsibilities:
Pre-Trial:
Identify and qualify potential clinical trial sites and investigators.
Set up and equip trial sites with necessary materials and equipment.
Train site staff on study procedures and data collection methods...
...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...
...Associate Clinical Data Manager
SDC is a team of diversified professionals who deliver exceptional Biometric Services, Consulting, and Technology... ...-ready clinical study documentation within the electronic Trial Master Files for multiple projects
The above...
Summary
To lead a community of ~ 20 Clinical Data Acquisition Specialists, Clinical Data... ...Clinical Data Acquisition and Management associates/roles (Clinical Data Scientists, Clinical... ...the right decisions to solve issues at the trial/program delivery level.
•Understands...
...and tracking of TMF QC activities.
• Execute trial TMF QC activities in accordance with TCO portfolio and Clinical Operations Transition Decision Point (TDP) and Clinical... ...and governances. May perform Clinical Project Associate (CPA) tasks as assigned
Commitment to...
