1 - 20 of 32 Jobs

Clinical Systems (Veeva) Tester W/ CDMS (EDC)

Key Business Solutions, Inc.

Remote

Third Party, Contract

Clinical Systems (Veeva) Tester W/ CDMS (EDC) Remote 12 Months Consultant should be work in offshore(India timings) We are looking for a well-rounded Clinical Systems Tester with core expertise in Veeva CDMS (EDC) and strong hands-on experience with eCOA and IRT platforms. This role supports testing and validation activities within a Decentralized Clinical Trial (DCT) environment, requiring flexibility across various digital systems and patient-facing technologies. Key Responsibilities: Author a

Clinical Data Coder (Remote, Part-Time)

Real Soft, Inc / Diversity Direct

Remote

Part-time

Job Overview We are seeking a detail-oriented and technically proficient Clinical Data Coder to support the accurate and timely coding of medical and medication terms within our electronic data capture (EDC) systems, primarily Rave Coder. This part-time remote role plays a vital part in ensuring data integrity and regulatory compliance across oncology clinical trials. Job Duties and Responsibilities Perform ongoing medical and medication coding using Rave Coder in alignment with MedDRA and WHO D

Lead Data Engineer (Life Science/CRO/Biotech Domain)

Rivago infotech inc

Durham, North Carolina, USA

Full-time

Role: Data Lead with Life Science/ CRO exp Location: Research Triangle Park, NC 27709 (Hyrbid) Hire Type: Fulltime Experience: 10+ years of experience Must Have Skills Required: Architect with familiarity with clinical systems (e.g., EDC, eTMF, CTMS, SAS, Argus) and data standards (e.g., CDISC, STDM). Preferred Skills : Experience with cloud-based data platforms like Azure data bricks and worked on Data Architecture . Knowledge of machine learning and data analytics. Job Description: The Lead,

Data Management Sr Manager

Aditi Consulting

Remote or Thousand Oaks, California, USA

Contract

Payrate: $55.00 - $60.00/hr. Summary: To provide expertise in data management processes, demonstrating capabilities & new ways of working, to assist in the design and implementation of both new technologies, new processes. Responsibilities: Develop Data Management playbook to encompass new ways of working with key accountabilities defined and known, both internally within function as well as broader study team Assess and determine roles and responsibilities within the Data Management Team Cleans

Clinical Research Associate

Zachary Piper Solutions, LLC

Sacramento, California, USA

Full-time

Piper Companies is currently seeking an Oncology Clinical Research Associate (CRA) for an opportunity in Sacramento, California (CA). The Oncology Clinical Research Associate (CRA) will participate in ongoing Clinical Trials throughout the Country for a leading Clinical Research Organization. Responsibilities for the Oncology Clinical Research Associate: Conduct site and study visits and perform all site monitoring activities across multiple study Responsible for both remote and on-site monito

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

North Chicago, Illinois, USA

Full-time

Responsibilities: Liaise with stakeholders to understand clinical study data aggregation requirements. Use the analytics platform to set up the study for the processing of data from source and/or systems. Load data from EDC, and extract into the analytics platform map to SDTM and/or other custom data formats. Understand the protocol and eCRF document and prepare the SDTM specification. Interact with the study team to understand the study requirements. Understand and identify data loading options

Clinical Research Associate

Zachary Piper Solutions, LLC

Los Angeles, California, USA

Full-time

Piper Companies is currently seeking a Clinical Research Associate (CRA) for an opportunity in Los Angeles, California (CA). The Clinical Research Associate (CRA) will participate in ongoing Clinical Trials throughout the Country for a leading Clinical Research Organization. Responsibilities for the Clinical Research Associate: Conduct site and study visits and perform all site monitoring activities across multiple study Responsible for both remote and on-site monitoring and study activation

Technician Diesel Mechanic

Ryder System

Cedar Rapids, Iowa, USA

Full-time

Position Description Immediately hiring a Permanent Full Time Experienced Mid-Level Diesel Technician to support our Truck Fleet at Ryder in Cedar Rapids, Iowa For More Info Call Dominique or Text "Cedar Rapids T2" to Hear it from a Ryder Technician Employee Here: ;/p> Hourly Pay:?$26.25 per hour Certification Bonus of $100 for each New ASE Certification Obtained up to $700 Quarterly Bonus: Ryder Pays you up to $500 Every Quarter - Four Times Per Year Schedule: Monday?Friday Weekends OFF Hours

Clinical Research Coordinator

Zachary Piper Solutions, LLC

Raleigh, North Carolina, USA

Full-time

Piper Companies is seeking a highly organized and proactive Clinical Research Coordinator (CRC) to support clinical trials across multiple therapeutic areas on-site in the Raleigh, NC area. This role is essential in ensuring smooth trial execution within a clinical site network, with a focus on phlebotomy and patient coordination. Key Responsibilities of the Clinical Research Coordinator: Oversee day-to-day clinical trial activities while ensuring compliance with Google Cloud Platform, IRB, and

MTC Sustaining Lead Engineer

Micron Technology, Inc.

Boise, Idaho, USA

Full-time

Our vision is to transform how the world uses information to enrich life for all. Micron Technology is a world leader in innovating memory and storage solutions that accelerate the transformation of information into intelligence, inspiring the world to learn, communicate and advance faster than ever. The Micron Mask Technology Center (MTC) is an innovative photomask fabrication facility located in Boise, Idaho. We enable sophisticated photolithography through our fine-tuned photomask technology

Clinical Research Coordinator

Zachary Piper Solutions, LLC

Raleigh, North Carolina, USA

Full-time

Piper Companies is seeking a detail-oriented and proactive Clinical Research Coordinator (CRC) to join our growing clinical research team. The ideal candidate will have hands-on phlebotomy experience and a strong background working within a clinical site network environment. This role is essential in supporting the execution of clinical trials across multiple therapeutic areas. Responsibilities for the Clinical Research Coordinator: Coordinate and manage day-to-day clinical trial activities in

Review Engineer

City of New York

Queens, New York, USA

Full-time

Company Description Job Description The NYC Department of Environmental Protection (DEP) enriches the environment and protects public health for all New Yorkers by providing 1.1 billion gallons of high quality drinking water, managing wastewater and storm water, and reducing air, noise, and hazardous materials pollution. DEP is the largest combined municipal water and wastewater utility in the country, with nearly 6,000 employees. DEP's water supply system is comprised of 19 reservoirs and 3 c

Sr. SAS Programmer

Katalyst Healthcares and Lifesciences

Charlotte, North Carolina, USA

Full-time

Responsibilities: Lead the development and implementation of submission-ready SDTM datasets in accordance with regulatory requirements (e.g., FDA, EMA, PMDA). Collaborate with regulatory affairs and quality assurance teams to ensure compliance with submission guidelines and standards. Perform thorough quality control checks to validate the accuracy and completeness of submission datasets. Coordinate the preparation and documentation of submission packages, including data specifications and v

Senior Manager Data Management

Katalyst Healthcares and Lifesciences

San Diego, California, USA

Full-time

Responsibilities: Responsible for data management documentation, including, but not limited to data management plan(DMP), CRF, eCRF design, edit check specifications, data issue logs, and data review plans and ensures all documents follow study design and regulatory requirements. Maintain Data Management outsourcing metrics and key performance indicators to aid the selection of CRO partners / Vendors and the ongoing management of partnerships. Participate in vendor qualifications and audits.

Clinical Data Lead - Vaccines

Sanofi U.S.

Morristown, New Jersey, USA

Full-time

Job Title: Clinical Data Lead - Vaccines Location: Morristown, NJ About the Job The Clinical Data Lead adapts and coordinates the data management strategy during development and conduct of clinical studies/projects for the mRNA/vaccine team within Sanofi. In addition, the Clinical Data Lead ensures data integrity and quality for clinical studies in order to deliver a comprehensive clinical database, and contributes to the optimization of data management processes and innovations. We are an i

Global Study Data Leader

Sanofi

Cambridge, Massachusetts, USA

Full-time

Job Title: Global Study Data Leader Location: Morristown, NJ Cambridge, MA About the Job Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate Progress. Global Study Data Leader is responsible for leading the end-to-end data management activities and associated quality deliverables for clinical trials including study set-up, conduct

Global Study Data Leader

Sanofi

Morristown, New Jersey, USA

Full-time

Job Title: Global Study Data Leader Location: Morristown, NJ Cambridge, MA About the Job Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate Progress. Global Study Data Leader is responsible for leading the end-to-end data management activities and associated quality deliverables for clinical trials including study set-up, conduct

Computer System Validation Analyst - R Studio & Clinical Systems

Katalyst Healthcares and Lifesciences

Remote or New Jersey, USA

Full-time

Responsibilities: Lead validation planning, risk assessment, and execution for R Studio, GitLab, and Medidata Rave EDC. Develop and execute validation documentation including: Validation Plans (VP.). User Requirements Specifications (URS.). Risk Assessments (RA.). Functional and Design Specifications. Traceability Matrix (RTM.). Test Protocols (IQ/OQ/PQ or CSA-based scripts.). Validation Summary Reports (VSR.). Collaborate with cross-functional stakeholders including Clinical Data Mana

Lead Data Engineer

Takeda pharmaceutical

Boston, Massachusetts, USA

Full-time

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description Pursuant to Section 20 C.F.R. 656.10, you are hereby notified that an application for Alien Employment Certification will be filed by

Data Manager MedRA Coder (WHODrug)

General Dynamics

Frederick, Maryland, USA

Full-time

Type of Requisition: Pipeline Clearance Level Must Currently Possess: None Clearance Level Must Be Able to Obtain: None Public Trust/Other Required: NACI (T1) Job Family: Medical Affairs Job Qualifications: Skills: Clinical Data Management, Electronic Data Capture (EDC), MedDRA Coding, WHODrug Certifications: None Experience: 5 + years of related experience ship Required: Yes Job Description: GDIT's Military Health team is hiring Data Manager MedRA Coder (WHODrug) to support the Office of