15 Oracle Inform Jobs

Description Senior Clinical Programmer (Veeva CDB) Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem ...

Imaging Endpoints (IE) is an Imaging Technology and Imaging Clinical Research Organization (iCRO). We are passionately focused on our vision to Connect Imaging to the CureTM . Everything we do is aligned with this singular purpose. We work every day excited to advance imaging science, technology, and services to bring curative technologies to humankind. We have supported many of the most impactful new drug approvals in oncology, and we are seeking the most talented individuals globally that are passionate in their desire to assist us in our mission to customize each clinical trial's imaging to optimize the opportunity to demonstrate efficacy. Imaging Endpoints is based in Scottsdale, Arizona...

As an experienced Technical Service Specialist at Fortrea, your role will involve assisting in the development and implementation of solutions to global technical service issues related to EDC, SAS, and other proprietary software. You will be responsible for developing and validating Custom/Complex SDTM/SAS datasets, listings, and reports, as well as efficiently handling external data and data reconciliations. Additionally, you will configure and implement EDC services within assigned projects to ensure project integrity and timely delivery of high-quality data. You may also act as a technical liaison with project team members, clients, and Data Managers to ensure the successful technical de...

Description Sr Clinical Programmer (EDC Programming-Rave/Veeva) Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passio...

Role Overview: As a Senior Clinical Programmer at Syneos Health, you will play a crucial role in accelerating customer success by translating clinical, medical affairs, and commercial insights into outcomes. You will be part of a team that puts the customer and patient at the center of everything they do, aiming to simplify and streamline work processes for enhanced collaboration and innovation. Your contributions will be pivotal in helping customers achieve their goals and ultimately changing lives. Key Responsibilities: - Utilize primary development tools such as Medidata, Rave, Oracle OC/RDC, Oracle Inform, and SAS to design, write, validate, and maintain software in adherence to specific...

Greetings from HCL Technologie! About the Company HCL Technologies is a global technology company that helps enterprises reimagine their businesses for the digital age. Our mission is to deliver technology solutions that drive business transformation and create value for our clients. About the Role We are looking for a talented individual to join our team and contribute to our mission of delivering innovative technology solutions. Responsibilities Bachelor's degree in Life Sciences, Computer Science, or related field. 6+ years of experience in clinical data testing and validation. Perform UAT for CRF screens, database edit checks, and exceptional reports/listings. Test clinical study setup c...

Key Responsibilities: Bachelor's degree in Life Sciences, Computer Science, or related field. 8+ years of experience in clinical data testing and validation. Perform UAT for CRF screens, database edit checks, and exceptional reports/listings. Test clinical study setup configurations including protocol parameters, visit schedules, and form designs. Validate external data acquisition (Lab, ECG, PK/PD) and ensure accurate processing. Collaborate with Clinical Data Scientists and Study Data Managers to understand study scope and expectations. Strong experience with clinical study setup and CDMS platforms and CTMS Review edit check specifications; write and execute UAT scripts. Conduct QC on meta...

Description Sr Clinical Programmer (EDC Programming-Rave/Veeva) Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passio...

**Urgent Hiring for the Role of Python AI Engineer Automated Test Data Generation for our team** Title: Python AI Engineer Automated Test Data Generation Experience: 8+years Location : Remote Timing: US EST Hours Overview We are seeking a Python AI Engineer with expertise in synthetic and automated test data generation to support clinical trials, regulatory submissions, and GxP-compliant systems across the life sciences domain. This role will focus on building intelligent frameworks that generate high-quality, audit-ready datasets for use in clinical data management (CDM), biostatistics, pharmacovigilance, and regulatory validation environments. By leveraging AI/ML techniques and Python-base...

Tools Required Rave Oracle Inform Veeva Studio Roles and Responsibilities Protocol reading and understanding Design the eCRF layout and the database corresponding to the eCRFs to hold the data from the EDC system Setup Core Configurations Implementing the Dynamic rules as per the Sponsor requirements Experienced in writing the Data Validation Specification (DVS) Create, test, and maintain trial-specific plausibility and consistency Edit Checks as per Data Validation Specification Analyze complex checks and Develop Custom Functions using C# for Rave studies or other EDC Expertise in performing Technical and Functional Review Incorporate internal feedback and update programs as required Must H...

Tools Required Rave Oracle Inform Veeva Studio Roles and Responsibilities Protocol reading and understanding Design the eCRF layout and the database corresponding to the eCRFs to hold the data from the EDC system Setup Core Configurations Implementing the Dynamic rules as per the Sponsor requirements Experienced in writing the Data Validation Specification (DVS) Create, test, and maintain trial-specific plausibility and consistency Edit Checks as per Data Validation Specification Analyze complex checks and Develop Custom Functions using C# for Rave studies or other EDC Expertise in performing Technical and Functional Review Incorporate internal feedback and update programs as required Must H...

Tools Required Rave Oracle Inform Veeva Studio Roles and Responsibilities Protocol reading and understanding Design the eCRF layout and the database corresponding to the eCRFs to hold the data from the EDC system Setup Core Configurations Implementing the Dynamic rules as per the Sponsor requirements Experienced in writing the Data Validation Specification (DVS) Create, test, and maintain trial-specific plausibility and consistency Edit Checks as per Data Validation Specification Analyze complex checks and Develop Custom Functions using C# for Rave studies or other EDC Expertise in performing Technical and Functional Review Incorporate internal feedback and update programs as required Must H...

As part of this role, you will be assisting in the development and implementation of solutions for global technical service issues related to EDC, SAS, or other proprietary software. Your responsibilities will include developing and validating Custom/Complex SDTM/SAS datasets, listings, and reports, as well as efficiently handling external data and data reconciliations. You will be responsible for configuring and implementing EDC services within assigned projects to ensure project integrity and on-time delivery of quality data. In addition, you will act as a technical liaison with project team members, clients, and Data Managers to drive the technical aspects of project delivery. You are exp...

Job Role: Clinical Database Programmer Exp: 03-15 Years Location: Gurgaon, Pune, Bangalore, Hyderabad, Chennai, Kochi, Mumbai Tools Required: Rave, Oracle Inform, Veeva Studio (Any One) Mandate Skills: Research and analytical skills: Ability to gather, interpret, and synthesize data into insightful information. Attention to detail: Ensuring accuracy and adherence to guidelines such as Protocol, Specification, Library Standards, ICH GCP,etc. Looking for Clinical Database Programmer with a solid understanding of Clinical Protocol, Medical and Scientific Principles of conducting clinical trials. Analyze complex checks and Develop Custom Functions using C# for Rave studies or other EDC.

As a Clinical Database Programmer at ProcDNA, you will play a crucial role in designing the eCRF layout and corresponding database, implementing dynamic rules based on Sponsor requirements, and creating trial-specific Edit Checks. Your responsibilities will also include developing Custom Functions using C# for Rave studies or other EDC systems, incorporating internal and Sponsor feedback, and maintaining eCRFs and components as per protocol amendments or metadata updates. Additionally, you will support CRO trial activities, create reports using JReview, SAS, BOXI, and handle migration processes for Post Go-Live studies. To excel in this role, you must have a deep understanding of Clinical Pr...