Average salary: Rs252,380 /yearly
More stats ...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...
Job Description
Job Description
CTC II
Job Description
Job Description
Clinical CTC-1
...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...
...comprehensive PO creation, invoice management and PO reconciliation and PO closure across a variety of vendor categories including CROs, clinical trial sites, contract labs, IRB/EC and other key assignments. Collaborate cross-functionally to develop strong internal and external...
...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.
...
...comprehensive PO creation, invoice management and PO reconciliation and PO closure across a variety of vendor categories including CROs, clinical trial sites, contract labs, IRB/EC and other key assignments. Collaborate cross-functionally to strengthen strong internal and external...
...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...
...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...
...people first. We’re looking for people who are determined to make life better for people around the world.
The Trial Capabilities Manager provides clinical trial capabilities in support of clinical development. The Manager is accountable to ensure the investigator sites...
...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...
...individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research...
...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...
...role will provide functional and technical support to corporate clinical team in executing projects to support global clinical strategy.... ...tool.
• Support creation of global clinical metrics e.g. clinical trial dashboard, CER matrix etc.
• Provide support in writing corporate...
...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...
...in the healthcare industry? We are looking for a skilled Senior Clinical Programmer to join our Data Management Operations and Insights department... ...procedures and processes that may arise during clinical trials.
Qualifications
To be successful in this role, we...
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...
...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...
...Delivery team directs, coordinates and manages the technical and operational aspects of projects, securing the successful completion of clinical trials. The team is therapeutically aligned to respond better to our customer needs. The therapeutic scope includes Cardiovascular &...
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...
...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...
...Job Description
Department – Clinical Reporting GBS
Are you detail-oriented and experienced in compiling and publishing clinical... ...knowledge to create clear and impactful communications about clinical trials. In addition to writing and publishing regulatory documents, we...
...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...
...Job Description
Job Title: Clinical Data Manager II
Career Level - C
Introduction to Role:
Are you ready to make a significant... ...also be responsible for meeting Quality Compliance requirements, Trial Master File compliance for audit readiness, and performing User...