Average salary: Rs550,000 /yearly
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...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...
...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...
...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...
...limited to:
Represents GCS as a core member in the integrated Clinical Trial Team (iCTT); defines and advises the iCTT on the optimal... ...world. How can we
achieve this With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this...
...Roles And Responsibilities
Responsible for taking leadership to meet, collaborate and initiate clinical trials at various healthcare facilities.
Prepare documentation for seeking permission to initiate clinical trials.
Responsible for managing the healthcare facilities...
...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
...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...
...Job Summary:
The Manager of Clinical Trials will lead and oversee all clinical trial activities for our medical device portfolio, ensuring compliance with international regulatory standards for markets including the U.S. and Japan. The role requires extensive experience...
...looking for INTERNATIONAL-HEAD-BD-INSULIN for US & EUROPE MARKETS.
For their THANE division they are on the lookout for HEAD-CLINICAL TRIALS
CLINICAL HEAD
Role Overview:
As the Clinical Head, you will lead the clinical regulatory department, overseeing the...
...domain expertise in regulatory sciences, clinical research solutions, quality & compliance,... ...device programs.
The Principal Clinical Trial Transparency and Disclosure Specialist... ...for client-related operational activities associated with daily deliverables, managing client...
...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...
...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...
Role-heading clinical regulatory department
Handling execution of clinical trials and managing reports and managing team.Â
Responsible as acting Head of Clinical Trial DepartmentÂ
Planning of Clinical trials to complete within defined timeline.Â
Clinical strategic...
...changing. Those aren't words that are usually associated with a job. But working at Bristol Myers... ...Area Description
Associate Global Trial Managers, crossing all therapeutic areas... ...drive operational aspects of complex, global clinical research studies from concept to final...
...The purpose of the role of the Manager, Clinical Trial Transparency is to drive the delivery of activities related to data disclosure in GSK RD in the respective therapy area (Oncology, Specialty, Vaccines)
The role is accountable to ensure consistent, timely and complete...
Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company focused on developing cell therapies for patients suffering... ...how autoimmune diseases are treated
The Senior Clinical Trials Manager will be a key member of the Clinical Operations team, leading...
...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...
...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...
...Join our team of experts in regulatory and ethics submissions of clinical studies. You will focus on facilitating the start of research projects... ...Bangalore, India
Your role:
Prepare independently clinical trial submission dossiers for Regulatory and Regulatory Authorities,...
...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...
