14 Ecrfs Jobs

- Understand and follow study start-up, conduct, and close out activities per the standard process, which will be made known to Service Provider and to the Data Manager in advance and in writing by Baxter. - Act as a single point of contact from the Service Provider for the studies as assigned - Prepare/review eCRFs, Edit checks, and Custom Functions requirement document - Prepare or review edit checks requirement and functional test script document - Perform functional testing for eCRF/edit checks and Custom Functions - Identify reports and DM Tables requirements and prepare a report specification document - Review and provide feedback for study conduct activities performed by the Service P...

As a Clinical Data Manager at Imaging Endpoints, your primary responsibility will be to lead, direct, and conduct all clinical data management activities for each assigned clinical study. You will work closely with internal and external stakeholders to ensure the successful completion of clinical data management tasks. Your duties will include maintaining audit readiness, communicating project status to stakeholders, and conducting data management activities according to standard operating procedures. Key Responsibilities: - Serve as the primary clinical data management contact for assigned studies - Lead the processing of radiological images in accordance with SOPs - Create and maintain dat...

Represents Data Management as the clinical database and data management subject matter expert on Clinical Project Teams through the following: Attend Clinical Project Team meetings to gather business need requirements and translate to technical requirements Partner with other shared service functions such as Safety, Core Lab, etc. to gather business need requirements and translate to technical requirements Identify, analyze, propose solutions, and effectively resolve complex data issues by exercising appropriate judgment and collaborating with the clinical project team members and other shared service functions Train database End Users (internal and external users) on the database and/or mai...

JOB DESCRIPTION: Represents Data Management as the clinical database and data management subject matter expert on Clinical Project Teams through the following: . Attend Clinical Project Team meetings to gather business need requirements and translate to technical requirements . Partner with other shared service functions such as Safety, Core Lab, etc. to gather business need requirements and translate to technical requirements . Identify, analyze, propose solutions, and effectively resolve complex data issues by exercising appropriate judgment and collaborating with the clinical project team members and other shared service functions . Train database End Users (internal and external users) o...

- Understand and follow study start-up, conduct, and close out activities per the standard process, which will be made known to Service Provider and to the Data Manager in advance and in writing by Baxter. - Act as a single point of contact from the Service Provider for the studies as assigned - Prepare/review eCRFs, Edit checks, and Custom Functions requirement document - Prepare or review edit checks requirement and functional test script document - Perform functional testing for eCRF/edit checks and Custom Functions - Identify reports and DM Tables requirements and prepare a report specification document - Review and provide feedback for study conduct activities performed by the Service P...

Position: Clinical Database Programmer *** JOB DESCRIPTION *** OVERVIEW The Clinical Programmer is responsible for developing and maintaining clinical trial programming, ensuring data integrity, and supporting data analysis for clinical studies. The role involves working closely with biostatisticians, clinical data managers, clients and other stakeholders to ensure that all programming tasks are executed accurately and efficiently across all Biometrics Services projects. The Clinical Programmer is accountable for quality, timely and efficient delivery of project programming tasks and quality information management. KEY TASKS & RESPONSIBILITIES • Read and understand clinical study protocols t...

As a Clinical Research Coordinator at Analytical Project, St. John's Research Institute in Bangalore, your role will involve interaction with patients, Sponsor/CRO, IEC, Lab staff, and other departments in the institution. You will conduct the study according to ICH GCP Guidelines, SOPs, and study protocol guidelines. Your main responsibility will be to act as the main line of communication between patients, Investigators, and CROs in study conduct activities. **Key Responsibilities:** - Coordinate in screening, Audio-Video consenting, enrollment, periodic study visits, and close-out visits. - Ensure that rights and well-being of a research participant are protected throughout the study dura...

As a Clinical Research Coordinator at Analytical Project, St. John's Research Institute in Bangalore, you will be responsible for interacting with patients, sponsors, IEC, lab staff, and other departments to conduct studies following ICH GCP Guidelines, SOPs, and study protocol guidelines. You will act as the main communication line between patients, Investigators, and CROs during study conduct activities. **Key Responsibilities:** - Coordinate in screening, Audio-Video consenting, enrolment, periodic study visits, and close out visits. - Ensure the protection of the rights and well-being of research participants throughout the study duration. - Coordinate with finance, legal, and regulatory...

Imaging Endpoints (IE) is an Imaging Technology and Imaging Clinical Research Organization (iCRO) passionately focused on the vision to Connect Imaging to the CureTM. Everything is aligned with this singular purpose, advancing imaging science, technology, and services to bring curative technologies to humankind. The organization has been instrumental in supporting impactful new drug approvals in oncology and is seeking talented individuals globally to assist in customizing each clinical trial's imaging for optimal efficacy. Imaging Endpoints, headquartered in Scottsdale, Arizona, with offices in various global locations, is affiliated with HonorHealth and Scottsdale Medical Imaging Limited (...

Designation: Clinical Data Management Full Time Opportunity Location: Multiple Job Description: - Understand and follow study start-up, conduct, and close out activities per the standard process, which will be made known to Service Provider and to the Data Manager in advance and in writing by Baxter. - Act as a single point of contact from the Service Provider for the studies as assigned - Prepare/review eCRFs, Edit checks, and Custom Functions requirement document - Prepare or review edit checks requirement and functional test script document - Perform functional testing for eCRF/edit checks and Custom Functions - Identify reports and DM Tables requirements and prepare a report specificatio...

- Understand and follow study start-up, conduct, and close out activities per the standard process, which will be made known to Service Provider and to the Data Manager in advance and in writing by Baxter. - Act as a single point of contact from the Service Provider for the studies as assigned - Prepare/review eCRFs, Edit checks, and Custom Functions requirement document - Prepare or review edit checks requirement and functional test script document - Perform functional testing for eCRF/edit checks and Custom Functions - Identify reports and DM Tables requirements and prepare a report specification document - Review and provide feedback for study conduct activities performed by the Service P...

Location - Bangalore/Cochin/Kochi/Hyderabad/Karnataka/Kerala/Mysore/Telangana - Understand and follow study start-up, conduct, and close out activities per the standard process, which will be made known to Service Provider and to the Data Manager in advance and in writing by Baxter. - Act as a single point of contact from the Service Provider for the studies as assigned - Prepare/review eCRFs, Edit checks, and Custom Functions requirement document - Prepare or review edit checks requirement and functional test script document - Perform functional testing for eCRF/edit checks and Custom Functions - Identify reports and DM Tables requirements and prepare a report specification document - Revie...

- Understand and follow study start-up, conduct, and close out activities per the standard process, which will be made known to Service Provider and to the Data Manager in advance and in writing by Baxter. - Act as a single point of contact from the Service Provider for the studies as assigned - Prepare/review eCRFs, Edit checks, and Custom Functions requirement document - Prepare or review edit checks requirement and functional test script document - Perform functional testing for eCRF/edit checks and Custom Functions - Identify reports and DM Tables requirements and prepare a report specification document - Review and provide feedback for study conduct activities performed by the Service P...

- Understand and follow study start-up, conduct, and close out activities per the standard process, which will be made known to Service Provider and to the Data Manager in advance and in writing by Baxter. - Act as a single point of contact from the Service Provider for the studies as assigned - Prepare/review eCRFs, Edit checks, and Custom Functions requirement document - Prepare or review edit checks requirement and functional test script document - Perform functional testing for eCRF/edit checks and Custom Functions - Identify reports and DM Tables requirements and prepare a report specification document - Review and provide feedback for study conduct activities performed by the Service P...