Clinical Data Coder

Job Summary: Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Data Reviewer in Mumbai, India to join our Global Clinical Coding & Support team. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where...

Excellent communication skills, both verbal and written. We are looking for a Medical Coder to join our team to assist us in coding for insurance claims and databases. The Medical Coder will display motivation, be detail-oriented and have outstanding people skills that help them navigate any situation with ease. Roles and Responsibilities - Account for...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

Opportunity to work on interesting client problem statementsWorking closely with exec leaders across Digital/Data Technology and BusinessAbout Our ClientOur client is an Insights-driven technology and data company specializing in Personalized Medicine, Evidence Generation, and Real-World Evidence Research powered by Next-Gen AI platforms, research-grade deep...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

Opportunity to work on interesting client problem statements Working closely with exec leaders across Digital/Data Technology and Business About Our Client Our client is an Insights-driven technology and data company specializing in Personalized Medicine, Evidence Generation, and Real-World Evidence Research powered by Next-Gen AI platforms,...

May support LDM with the review, maintenance and update of External Vendor data received from central vendor or local laboratories. Working to ensure department SOPs, guidelines and global standards are followed to maintain data integrity and ensure consistency across all projects. Ensure electronic vendor data contains all protocol specified parameters, is...

**Essential Job Duties**: - The below statements are intended to describe the general nature of the job and are not intended to be an exhaustive list of all responsibilities, skills and duties. - Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study...

**Job Summary**: The Clinical Research Associate II (CRA II) is responsible and accountable for site monitoring and site management. Has responsibility for clinical studies according to Company, and/or Sponsor Standard Operating Procedures, and local regulatory guidelines. Assures the implementation of project plans, as assigned. Act in the project role of a...

Job Summary: - Site management responsibility for clinical studies according to Labcorp Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. - Conducts site monitoring responsibilities for clinical trials according to Labcorp Standard Operating Procedures...

**Essential Job Duties**: 1) Document and track study activities using relevant forms and tools, as well as relevant Project Management Systems with guidance/support 2) Assist in the preparation of study and site specific materials in accordance with relevant SOPs 3) Complete minute taking and documentation for sponsor/external or internal teleconferences...

Develop SAS macros, templates and utilities for data cleaning and reporting. ? Utilize SDTM guidelines to build datasets. ? Identify and edit checks per the data validation plan or data management plan. ? Utilize SAS programming skills within protocol team and perform all programming required for clinical trial analysis and reporting. **Job Types**:...

**Data Scientist, Global Data Science & Analytics**: For years, Abbott’s medical device businesses have offered technologies that are faster, more effective, and less invasive. Whether it’s glucose monitoring systems, innovative therapies for treating heart disease, or products that help people with chronic pain or movement disorders, our medical device...

Associate Clinical Data Processor Bachelor’s Degree in any stream or Final Year Appeared with zero to one year of experience in performing data entry activities. Experience in MS Office; additional Certification in MS-Office or Microsoft Office Specialist (MOS) certification will be an asset. Ability to read, write and speak in English; English proficiency...

Job Summary: Our global activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Database Programmer to join our Biometrics team. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and...

Overview:As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements, and industry standards throughout the trial process.Responsibilities:1 . Trial...

Role Overview :The Clinical Development incumbent will be responsible for the oversight of development and execution linked to worldwide clinical development plans for the assigned programs in portfolio focussed on Oncology and innovative in-licensed assets. The incumbent will be responsible for integrating clinical development objectives with global...

Overview:As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements, and industry standards throughout the trial process.Responsibilities:1.Trial...

Overview:As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements, and industry standards throughout the trial process.Responsibilities:1.Trial...

Overview: As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements, and industry standards throughout the trial process. Responsibilities: 1 . Trial...