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...and you’ll be helping shape an industry. The role:
The Clinical Trial Manager is responsible for the delivery of all clinical aspects of... ...origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for...
...Job Description
Department – Clinical Medical Regulatory (CMR)
Do you want to be a part of a high performing team in Novo Nordisk... ...inspiring working environment, you may be our new Project Manager (CDC Trial Manager) for the Clinical Medical Regulatory team based at...
New Doc 03-20-2024 16.11.pdf
...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...
...and you’ll be helping shape an industry. The role: The Clinical Trial Manager is responsible for the delivery of all clinical aspects of... ...origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for...
Remote job
...affordable healthcare & ensure patients have access to state-of-the-art medical care.
Their HQ & R&D centres are in Thane, with an office in... ...their THANE division they are on the lookout for HEAD-CLINICAL TRIALS
CLINICAL HEAD
Role Overview:
As the Clinical Head, you...
...Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of...
...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...
...protocols, amendments and related documents; drive and/or supprt trial-related documents and processes.
development of clinical section... ..., reporting and publishing activities (either at a local medical organization, investigational site, pharmaceutical company/CRO, or...
...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...
...clinical studies.
Perform quality control of documents submitted to the eTMF using the established acceptable criteria
Ensure clinical trial documentation is consistent with eTMF specifications, ICH-GCP guidelines, regulatory requirements, and applicable SOPs
Address eTMF...
...Sun is seeking a Global Trial Manager, Clinical operations within its clinical development Team in India. The Global Trial Manager, Clinical... ...teams-
Coordinate with cross functional teams (e.g. Medical monitor, Regulatory Affairs, supply chain, statistics, Data management...
...sense, the ability to work quickly and under pressure, and a knack for getting things done in partnership with other teams
Department: Trial Business
Job Type: Full–Time (Work from Office)
Location: Bangalore
Reporting to: Deputy Manager – Trial Business...
...Requirements
BA/BS or Associate degrees in relevant discipline
Experience Requirements Experience in the use of industry Clinical Trial Management Systems and
Clinical Trial Master File Systems is a plus.
Experience in Clinical Research or related work experience....
...are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe... ...~ Full range of clinical trial services to biopharmaceutical, medical device, and diagnostic customers, for all trial phases, registration...
Job Description
Job Description
• Administers the daily financial management of simple or moderately complex studies, for the functional area's portion of a project budget, as assigned with minimal supervision.
• Performs review of contract and bidding assumptions...
...Manages performance and career development of Global Trial Specialists (may include Associate Global Trial Managers). Member of the Department Leadership Team focused on development, accountability, and success of team members.
Leads or contributes to department process...
...clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end... ...high-profile drug and device programs.
The Principal Clinical Trial Transparency and Disclosure Specialist position is responsible...
...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 team to develop and implement data...
...of innovation.
Position Summary:
This individual contributor role has task-level responsibility for document and CTA (Clinical Trial Application) package creation which support all BMS Clinical Trials across the enterprise and engages closely with clinical trial vendors...
