...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
...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...
...scholar rock to protein structures, the clinical-stage company is focused on advancing innovative... ...of Position:
The Senior Clinical Trial Manager is responsible for all... ...the study, the Clinical Trial Manager may coordinate the activities of several other clinical...
...We are looking for a dedicated EU Submission Lead for Clinical
Trials to join our Global Regulatory Affairs team.
If you are... ...Professional, you will play a crucial role in
driving, coordinating, and actively following up on multiple
tasks with challenging...
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.
...
...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 the generation of accurate, complete, and consistent clinical databases.
To fulfil his/her job responsibilities in accordance... ...Plan (DMP) and Data Validation Plan (DVP) for assigned trials which include taking an active part in any review meetings....
...Clinical Trial Foundations (CTF), as part of Clinical Design, Delivery and Analytics (CDDA), delivers innovative and reliable systems, processes... ...systems.
• Provide technical knowledge and help with the coordination of all business system support, maintenance, and deployment...
...We are seeking a motivated and detail-oriented Clinical Research Coordinator to join our dynamic team. As a Clinical Research Coordinator, you will play a crucial role in the planning, implementation, and coordination of clinical research studies. You will work closely with...
...As a Clinical Care Coordinator, you will:
Verify patient call details through IVR.
Assign specific providers to patients based on symptoms and availability.
Utilize appropriate tools and applications.
Coordinate between patients and providers to set up treatment...
...We are seeking a detail-oriented and organized individual to join our team as a Client Invoicing Coordinator. As a key member of our order management department, you will play a crucial role in ensuring accurate and timely invoicing for our clients. The ideal candidate will...
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...
...We are currently seeking a dedicated Clinical Coordinator to join our team. As a Clinical Coordinator, you will play a vital role in overseeing all administrative tasks within our organization. This includes warmly welcoming patients as they check-in to our facility, ensuring...
...world-leading healthcare intelligence and clinical research organization. We’re proud to... ...and guide less experienced clinical data coordinators in data management requirements and activities... ...Provides DM leadership across assigned trial(s) Acts as the Trial Data Manager (CDL) where...
...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 Product (IP) and trial materials....
...Clinical Research Coordinator
About the job
Role Description
This is a fulltime hybrid role for a Clinical Research Coordinator with Client... ...research clinical research experience and clinical trials. This role is located in Bengaluru but offers flexibility 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...
...Department – Clinical Medical Regulatory (CMR)
Do you want to be a part of a high performing... ...completion of the clinical programme.
Coordinating with CRM and RTM and communicates to them... ...and critical issues that may impair trial progress. In some cases, the CRA may have...
...and the UK, our 700+ people support 245+ active projects and clinical trials across 50+ countries, with 400+ more staff across our social enterprises... ...adherence to all relevant regulations and protocols.
- Coordinate with cross-functional teams, including investigators,...
Summary
Drive and execute labelling activities for clinical trial supplies (IMP) to ensure fulfillment of supply chain. Resulting in no... ...but are not limited to:
· Is responsible for generation/coordination of labels for IMP, medication list/randomization list/randomization...
...Clinical Team Leader will be responsible for overseeing the monitoring and site management activities on assigned clinical research... ...errors and study trends. Accountable for all study and coordination with trial site related activities to the assigned CPM and the sponsor...
...week).
- Daily on boarding activity to ward nurses.
- Data management and hospital data validation as per Dozee Device.
- Coordination with Remote team and inform about device related activities conducted during the visit.
- Build and manage relationships with ward...
...passion for scientific rigor and decades of clinical development experience Fortrea provides... ...update/review and approve all required trial data management documentation; including... ...initiate process review as appropriate.
Coordinate with DM study team to ensure the receipt...
...renowned Edu-Tech Start-up in Bangalore that offers comprehensive clinical research education with hands-on experience, industry... ...Relevant experience includes a minimum of 2+ years of clinical trials coordination and/or management experience.
• A minimum of 2+ years of experience...
Empower Research and Training Institute
Bangalore
1 day ago
...Job Description
Department – Clinical Reporting GBS
Are you detail-oriented and experienced... ...impactful communications about clinical trials. In addition to writing and publishing... ...final documents according to SOPs.
Coordinate and ensure the quality of appendices of...
Summary
That’s how many patients participate in our clinical trials at any given time. GCO is Novartis’ powerhouse of Global Clinical Operations... ...queries, proactively identifies query resolution issues, Coordinates the study handover process with CRAs and their managers to...
...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...
...Overview:
The Senior Clinical Data Programming role is either part of the Clinical Data... ...delivery to the study teams to file in the Trial Master File.
Completes study database... ...and CTMS.
Serves on project teams to coordinate and lead CDMS activities for clinical database...
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