Average salary: Rs382,777 /yearly
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...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...
...the study specific eTMF plans for assigned clinical studies.
Perform quality control of... ...established acceptable criteria
Ensure clinical trial documentation is consistent with eTMF... .../ or other functional teams as needed
Assist with inspection/audit related activities (...
...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
...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...
...What You Will Be Doing
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...
...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 collaboration... ...related documents; drive and/or supprt trial-related documents and processes.
development... ...procedures: attend CTT meetings, assist in report study progress and issues.
support...
...Sun is seeking a Global Trial Manager, Clinical operations within its clinical development Team in India. The Global Trial Manager, Clinical Operations... ..., the Global Trial Manager, Clinical Operations will assist Global Trial leader in providing global, regional or complex...
...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 GSK RD in the respective therapy area (Oncology, Specialty, Vaccines)
The role is accountable to ensure consistent, timely and complete...
...product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance,... ...high-profile drug and device programs.
The Principal Clinical Trial Transparency and Disclosure Specialist position is responsible for...
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...
...We are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and... ...internal and external contacts.
Key Accountabilities :
Assists in coordination of feasibility process with activities that...
...experts in regulatory and ethics submissions of clinical studies. You will focus on facilitating... ...role:
Prepare independently clinical trial submission dossiers for Regulatory and... ...regulatory training to project teams.
Assist with feasibility research and business development...
...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...
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...
...We are looking for Clinical Assistant to join our dynamic team and embark on a rewarding career journey
Take vital signs and record medical histories of patients, and update electronic medical records as needed
Assist physicians or other medical professionals in clinical...
...Fortis Healthcare Ltd is looking for Assistant Clinical Research to join our dynamic team and embark on a rewarding career journey As an Assistant... ...and recruitment of eligible participants for clinical trials, including obtaining informed consent and ensuring adherence to...
