...Responsible for taking leadership to meet, collaborate and initiate clinical trials at various healthcare facilities.
Prepare documentation... ...on the successful completion of the clinical program.
Coordinates with PM and communicates to them progress and critical issues...
...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...
...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...
...life. We are looking for a dedicated EU Submission Lead for Clinical Trials to join our Global Regulatory Affairs team.
If you are passionate... ...Professional, you will play a crucial role in driving, coordinating, and actively following up on multiple tasks with challenging...
...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...
...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
...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...
...of the LCTL/CTL, as assigned. Support the clinical protocol development process in... ...and related documents; drive and/or supprt trial-related documents and processes.
development... ...and internal/external presentations.
coordinate the real time availability of quality clinical...
...We are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe... ...project team to help manage clinical trial feasibility processes, coordinate clinical trial start-up activities including collection of...
...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 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...
...About The Role
Your responsibilities will include, but are not limited to:
Represents GCS as a core member in the integrated Clinical Trial Team (iCTT); defines and advises the iCTT on the optimal clinical trial supply strategy in terms of, but not limited to, packaging...
...The purpose of the role of the Manager, Clinical Trial Transparency is to drive the delivery of activities related to data disclosure in... ...documents amongst the different Service providers involved
Coordinate workload distribution and establish/ maintain a robust communication...
...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....
...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...
...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...
...Role Description
This is a full-time hybrid role for a Clinical Research Coordinator with Learning Lab. The Clinical Research Coordinator will be... ...protocols, research, clinical research experience, and clinical trials. This role is located in Bengaluru but offers flexibility...
...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...
...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...
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... ...systems.
• Provide technical knowledge and help with the coordination of all business system support, maintenance, and deployment...
...careers.bms.com/working-with-us.
Key Responsibilities
The Document Coordinator is responsible for managing and executing on centralized activities in support of global trials with an emphasis on clinical documentation.
The Document Coordinator will interact with...
...Sun is seeking a Global Trial Manager, Clinical operations within its clinical development Team in India. The Global Trial Manager, Clinical... ...documents, monitoring study progress and data quality and coordinating trial tasks and timelines, ensuring all teams and tasks are...
Experience: 12 years + Schedule: Full-Time
Education: Degree in Life science/Pharma, business, marketing or related field.
Skills & Job Description:
1.      Good Communication & interpersonal skills, negotiation skills, research and strategy, business intelligence...
...Octalsoft Job Requisition: Sales Director- eClinical Solutions (SaaS) for Clinical Operations (Clinical Trials) Octalsoft is a leading SaaS company specializing in eClinical Solutions for the Clinical Research industry. Our innovative software platforms empower organizations...
Fortis Healthcare Ltd is looking for Clinical Research Coordinator to join our dynamic team and embark on a rewarding career journey
We are seeking... ...for participant recruitment and enrollment in clinical trials
Obtain informed consent from eligible participants and ensure...
...Anonymisation provides a critical role in the preparation of anonymised clinical documents to meet GSK s clinical document disclosure obligations... ...in matrix organization
Experience in managing clinical trial (study, data, or system/technology) activities.
Good understanding...
...Note Only male candidates can apply for this job
Job Description Clinical Coordinator
Overview
We are seeking a highly motivated and experienced person to join our team
Responsibilities:
Visit hospitals and patient s homes to setup devices
Conduct site recce...
...Job description
Department - Clinical Medical Regulatory (CMR)
Do you want to be a... ...you may be our new Project Manager (CDC Trial Manager) for the Clinical Medical Regulatory... ..., quality audits and inspection issues. Coordinate, in partnership with the COM (Clinical Operation...
...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...