Clinical Research Coordinator

**Job Type - Fresher or Internship level** Clinical Research Associates manage clinical trials and studies pertaining to biotechnological and pharmaceutical products, drugs and procedures. A Clinical Research Associate, also known as a CRA, conducts research to ensure these products are safe. **Responsibilities**: **1. Assist in Protocol Development**: -...

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...

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...

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...

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...

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...

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...

**Responsiblities**: - Provide clinical study start up expertise. - Assist Lead CRA in the preparation of IRB submissions including the review of the sitespecific informed consent and assent forms - Track IRB submissions - Collect, review, and process essential documents and identify issues that site needs to address. - Communicate to site the updates...

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...

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...

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...

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...

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...

Create content pieces that appeal to our audiences, attract customers and boost our brand awareness. - Produce content marketing campaigns to drive leads and subscribers. - Utilize SEO best practices to generate traffic to our website. - Oversee our website, promote our blog and pitch articles to third-party platforms effectively. - Work together with...

**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,...

Develop clinical pharmacy programs according to policies and regulations - Review records of patients to determine the appropriateness of medication therapy - Evaluate patient’s condition to ensure all issues are being treated - Identify untreated health problems and refer patients to appropriate physicians - Develop effective medication plans that...

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...