Remote Clinical Data Programmer I role in New Haven, CT. Provide advanced data management support to internal study and scientific teams. Develop data collection forms for multiple imaging modalities. Create data cleaning programs and custom calculat...
Seeking dedicated individuals for Data Entry roles supporting diverse projects like cataloging products, evaluating clinical trial data, and analyzing feedback. Flexibility to work remotely or in-office with benefit of choosing ideal hours. Applicant...
Exciting part-time opportunity for Clinical Statistician II. Join our expanding clinical team in Santa Clara, CA, supporting the Structural Heart division. Provide statistical expertise for clinical data sets, contributing to podium presentations and...
Seeking dedicated individuals for Data Entry roles supporting various projects locally and nationally. Essential for accurate data handling across sectors like product cataloging and client feedback analysis. Flexible remote/on-site opportunities for...
Seeking a Clinical Research Monitor for overseeing Alliance Foundation Trials sites, ensuring data validation, ISF reconciliation, and protocol adherence. Collaborate with project teams, manage monitoring activities, ensure GCP compliance, and handle...
Holiday work
Full time
Remote job
Boston, MA
Alliance for Clinical Trial in Oncology Foundation
Seeking a Clinical Data Programmer I for remote work in New Haven, CT. Role involves crafting data forms, writing cleaning programs, and creating custom validation routines. Must have strong analytical skills, CDISC knowledge, and familiarity with Gx...
"The Markey Cancer Center seeks a Research Associate Clinical I in Lexington, KY for managing clinical trial data. Responsibilities include organizing workflow, ensuring compliance with FDA and IRB, and preparing for monitoring visits. Hybrid work op...
Seeking a Specialist for Clinical Trial & Data Management at University of Iowa. Responsibilities include protocol development, subject recruitment, data collection, and regulatory compliance. Required: Master’s degree, 3-5 years clinical research ex...
Seeking meticulous individuals for Data Entry roles. Manage precise data for diverse projects. Remote/in-office options available. Key qualifications: tech-equipped, high-speed internet, attention to detail. Benefits include flexible hours, product p...
Seeking Remote Principal Statistical Programmer with 10+ years in Pharmaceutical/Biotech programming, including macro/tools dev. Strong SAS skills, FDA exp preferred. Manage projects, lead studies, automate programming activities. Full-time role, $12...
