Clinical Research Associate

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 Responsibilities : Conduct site visits to monitor trial activities and ensure compliance...

Responsibilities for Clinical Research Associate - Recruit and enroll study participants - Input clinical research data into electronic data systems - Coordinate patient visits and procedures related to research - Act as resource for study participants by answering questions and explaining related procedures - Ensure the study site is compliance with all...

Specific duties can vary depending on the company, but clinical research associates will generally be required to: - Develop trial procedures, methodology and instructions for clinical trials staff, as well as design data collection tools (case report forms) - Manage study supplies, drug supplies and drug accountability (and prepare study drugs for...

Creating and writing trial protocols, and presenting these to the steering committee. - Identifying, evaluating, and establishing trial sites, and closing sites down on completion of the trial. - Training site staff on therapeutic areas, protocol requirements, proper source documentation, and case report form completion. - Ordering, tracking, and managing IP...

Specific duties can vary depending on the company, but clinical research associates will generally be required to: - Develop trial procedures, methodology and instructions for clinical trials staff, as well as design data collection tools (case report forms) - Manage study supplies, drug supplies and drug accountability (and prepare study drugs for...

Fusion Market Research is hiring for Research Associate/ Research Analyst **Responsibilities** Key responsibilities: 1. Conduct Secondary / Primary research 2. Create Market Research report 3. Product research using search engine 4. Work on company profiling, SWOT analysis, Report writing, Article writing 5. Project delivery in market research, 6....

As a Clinical Research Associate, you will be responsible for managing and monitoring clinical trials. You will work closely with investigators to ensure that all aspects of the study are conducted according to protocol and in compliance with regulatory requirements. Your tasks will include preparing and reviewing study documents, ensuring adherence to...

As a Clinical Research Associate, you will be responsible for managing and monitoring clinical trials. You will work closely with investigators to ensure that all aspects of the study are conducted according to protocol and in compliance with regulatory requirements. Your tasks will include preparing and reviewing study documents, ensuring adherence to...

Schedule, Plan and Conduct Site Visits: Site Selection Visits, Site Initiation Visits, Interim Monitoring Visits and Site Close-out Visits. - Write Reports and Investigator Follow-up Letters for Site Visits: Site Selection Visits, Site Initiation Visits, Interim Monitoring Visits and Site Close-out Visits. - Compliances: Follow international GCP...

The Clinical SAS Programmer will lead the programming activities for various purposes including SAS Data Listings to be used for data review, Safety Review Listings, Centralized Monitoring Listings and Reports. The Clinical SAS Programmer will also be responsible for productions of Key Risk Indicators, working collaboratively across departments to produce...

The Clinical SAS Programmer will lead the programming activities for various purposes including SAS Data Listings to be used for data review, Safety Review Listings, Centralized Monitoring Listings and Reports. The Clinical SAS Programmer will also be responsible for productions of Key Risk Indicators, working collaboratively across departments to produce...

The Clinical SAS Programmer will lead the programming activities for various purposes including SAS Data Listings to be used for data review, Safety Review Listings, Centralized Monitoring Listings and Reports. The Clinical SAS Programmer will also be responsible for productions of Key Risk Indicators, working collaboratively across departments to produce...

develop and write trial protocols (outlining purpose and methodology) - present trial protocols to a steering committee - design data collection forms, known as case report forms (CRFs) - identify and assess the suitability of facilities to use as the clinical trial site - identify/select an investigator who will be responsible for conducting the trial at...

develop and write trial protocols (outlining purpose and methodology) - present trial protocols to a steering committee - design data collection forms, known as case report forms (CRFs) - identify and assess the suitability of facilities to use as the clinical trial site - identify/select an investigator who will be responsible for conducting the trial at...

Job description Fusion Market Research is hiring for Market Research Associate (Cross Domain) **Responsibilities**: Key responsibilities: 1. Conduct Secondary / Primary research 2. Create Market Research report 3. Product research using search engine 4. Work on company profiling, SWOT analysis, Report writing, Article writing 5. Project delivery in market...

Job Description: Junior Data Scientist (Breast Cancer Clinical Data) **Responsibilities**: - Knowledge of different information types and domains and aptitude to understand domains in the clinical field. - Some familiarity with GUI design and implementation and comfort with **python** is preferred. - Good communication skills and ability to work...

Monitoring clinical studies of investigational and approved products that have been determined to satisfy a medical need and/or offer a commercial benefit. This may include the following site visits: qualification, initiation, interim, and close out - Managing and training site personnel on therapeutic area, protocol requirements, proper source...

**Responsibilities**: - Creating and writing trial protocols, and presenting these to the steering committee. - Identifying, evaluating, and establishing trial sites, and closing sites down on completion of the trial. - Training site staff on therapeutic areas, protocol requirements, proper source documentation, and case report form completion. - Ordering,...

We're Hiring : AI ResearcherJob Location : PuneAre you passionate about leveraging cutting-edge AI technologies to drive innovation in healthcare? Join our team as an AI Researcher and be part of a dynamic environment where your expertise in Generative AI will shape the future of clinical decision-making.Job Description :As an AI Researcher specializing in...

We're Hiring : AI ResearcherJob Location : PuneAre you passionate about leveraging cutting-edge AI technologies to drive innovation in healthcare? Join our team as an AI Researcher and be part of a dynamic environment where your expertise in Generative AI will shape the future of clinical decision-making.Job Description :As an AI Researcher specializing...