Clinical Research Associate

**Clinical Research Trainee Position Overview**: A Clinical Research Trainee is an entry-level role within the field of clinical research, responsible for assisting in the planning, coordination, and execution of clinical trials and research studies aimed at evaluating the safety, efficacy, and effectiveness of new medical treatments, devices, and...

**Clinical Research Trainee Position Overview**: A Clinical Research Trainee is an entry-level role within the field of clinical research, responsible for assisting in the planning, coordination, and execution of clinical trials and research studies aimed at evaluating the safety, efficacy, and effectiveness of new medical treatments, devices, and...

Position Summary The Clinical Research Associate II (CRA II) will be a key contributor to AtriCure’s clinical affairs department and primarily responsible for the site management of assigned clinical investigative sites.The CRA II will assist with the implementation and execution of study protocols and associated study documents for clinical trials,...

**Responsibilities** - Interview patients and document basic medical history - Organize and schedule appointments, learn to coordinate Studies - Update and file medical records. - Arrange hospital admissions and laboratory services - Check with patients and type up patients charts - Produce and distribute correspondence memos, letters, faxes, and forms -...

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. **Responsibilities**: - Site Monitoring - SIV ~ COV - PI Management - audit & inspection - NDCT...

Relevant experience includes a minimum of 2+ years of clinical trials coordination and/or management experience. knowledge of FDA and other regulatory guidelines (e.g., ICH-GCP E6, HIPAA) that govern clinical research. A minimum of 2+ years of experience as a trainer, teacher, or instructor in clinical research, another medical field, or life sciences, OR...

DescriptionPrincipal Clinical ProgrammerSyneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide practical value to help our customers...

Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organization that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of...

ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.Responsibilities: Site Monitoring SIV ~ COV PI Management- audit & inspection NDCT...

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...

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...

**Requirements** - FOREIGN PHYSICIANS OR FOREIGN MEDICAL GRADUATES - CARE COORDINATION AND CASE MANAGEMENT EXPERIENCE HELPFUL - HOSPITAL AND VALUE BASED CARE COORDINATOR, RISK STRATIFICATION, MANAGED CARE EXPERIENCE HELPFUL **Primary Responsibilities**: - ED Communications and Relations - ED Admission Monitoring - TRC Coordination - Hospital Admission...

**Requirements** - FOREIGN PHYSICIANS OR FOREIGN MEDICAL GRADUATES - CARE COORDINATION AND CASE MANAGEMENT EXPERIENCE HELPFUL - HOSPITAL AND VALUE BASED CARE COORDINATOR, RISK STRATIFICATION, MANAGED CARE EXPERIENCE HELPFUL **Primary Responsibilities**: - ED Communications and Relations - ED Admission Monitoring - TRC Coordination - Hospital Admission...

Requirements FOREIGN PHYSICIANS OR FOREIGN MEDICAL GRADUATES CARE COORDINATION AND CASE MANAGEMENT EXPERIENCE HELPFUL HOSPITAL AND VALUE BASED CARE COORDINATOR, RISK STRATIFICATION, MANAGED CARE EXPERIENCE HELPFULPrimary Responsibilities: ED Communications and Relations ED Admission Monitoring TRC Coordination Hospital Admission Analysis Readmission...

Nutrition Research Associate About the role: As Nutrition Research Associate, you will work with the team at the Cuddles Institute of Clinical Nutrition to drive research and content development. This position will report to the - Responsibilities: - You’ll write well-researched, evidence-based, and informative nutrition content for our website, blog,...

The Clinical Data Coder is primarily responsible for providing support to activities related to coding of Clinical data for ongoing clinical studies. The Clinical Data Coder will also participate in various clinical data management activities required to ensure that data captured are collected, managed and reported clearly, accurately and securely. In...

As a (job title) you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence.What you will be doing: In general, a CRA would manage 12 sites but this could vary at individual assignment level considering the trial stage and complexity.Trial assignment will be performed by the MSOM in...

We are looking for experienced Indian clinical trial disclosure associates to join our dynamic, collaborative team to engage with biopharmaceutical clients to prepare and maintain clinical trial registry postings across global registries. This a full-time, remote opportunity. **About Us** Kateric (a Propharma group company) is a strategic partner for...