Job Opportunities
Description: Our client is looking for a Associate Director of Biostatistics. This individual will be responsible for directing the biostatistics activities for clinical studies for our sponsor client, including trial design, execution, analysis, and data interpretation, as well as working on SOPs and developing statistical methods sections of protocols. In addition, this person will be contributing to …
Your Mission: The Clinical Data Standards Manager is a key role on the Data Science team, composed of PhD/Masters statisticians, data scientists, analytical product leads, former FDA biostatisticians and computational genomicists. We leverage industry leading data assets and analytical models to transform the clinical development industry, driving scientific and operational success for our clients and partners. The Clinical Data …
The PLM Technology Sr. Project Manager/ Program Manager is a primary customer facing role that is responsible for managing related pre-sales activities, requirements gathering, solution planning, project execution, solution implementation, go-live and post go-live support, as well as project close and transition of support back to Customer IT & Business teams, according to strict deadlines …
Job Overview –The selected candidate will serve as the technical leader on all data management aspects for project(s) including start-up, maintenance, and completion activities and develop [Global] Data Management Plans and Quality Management (QM) Plans that will deliver accurate, timely, consistent, and quality clinical data.Additional responsibilities include: Identify and implement solutions to project data management …
Your Competencies: Review many hundreds to thousands of clinical trials data to form the metadata based data mining rules to search targeted domains and variables. Your Competencies: Review many hundreds to thousands of clinical trials data to form the metadata based data mining rules to search targeted domains and variables. Programming of data mining rules …
RESPONSIBILITIES: Lead all aspects of clinical data management for all concurrent projects from clinical study start-up to conduct and study closeout. Act as a consultant in data management processes and principles for all projects and other functional groups. Define and lead project management activities for multiple complex projects to bring clinical studies on-line Provide training, …
Job Summary Responsible for providing statistical programming support for the Biostatistics and Data Management functions for all clinical trials and regulatory submissions. Works closely with Biostatisticians and Data Managers to create SAS programs for independently validating selected tables, listings, and figures produced by programming vendors, for ad-hoc analyses, and to assist with data cleaning and …
RESPONSIBILITIES: Lead all aspects of clinical data management for all concurrent projects from clinical study start-up to conduct and study closeout. Act as a consultant in data management processes and principles for all projects and other functional groups. Define and lead project management activities for multiple complex projects to bring clinical studies on-line Provide training, …
Job Summary Responsible for providing statistical programming support for the Biostatistics and Data Management functions for all clinical trials and regulatory submissions. Works closely with Biostatisticians and Data Managers to create SAS programs for independently validating selected tables, listings, and figures produced by programming vendors, for ad-hoc analyses, and to assist with data cleaning and …
We are actively seeking a dynamic professional for a promising opportunity as Clinical Project Manager, will be responsible for working cross-functionally to develop the Clinical Strategy Plans to develop and conduct clinical research initiatives. Job Description Comprehensive study management for Post-Market clinical initiatives Ensure all research programs are conducted in accordance to approved project plan, …
RESPONSIBILITIES: Lead all aspects of clinical data management for all concurrent projects from clinical study start-up to conduct and study closeout. Act as a consultant in data management processes and principles for all projects and other functional groups. Define and lead project management activities for multiple complex projects to bring clinical studies on-line Provide training, …
Job Summary Responsible for providing statistical programming support for the Biostatistics and Data Management functions for all clinical trials and regulatory submissions. Works closely with Biostatisticians and Data Managers to create SAS programs for independently validating selected tables, listings, and figures produced by programming vendors, for ad-hoc analyses, and to assist with data cleaning and …
RESPONSIBILITIES: Lead all aspects of clinical data management for all concurrent projects from clinical study start-up to conduct and study closeout. Act as a consultant in data management processes and principles for all projects and other functional groups. Define and lead project management activities for multiple complex projects to bring clinical studies on-line Provide training, …
The QA Validation Specialist is responsible for oversight of validation activities on site ensuring compliance with current regulatory requirements. The QA Validation specialist will have specific and varying duties as assigned by the Quality Systems & Compliance Manager. Some key tasks and responsibilities are outlined below: RESPONSIBILITIES: Provide expertise in the area of validation at …
Aegis Technology Solutions is a world leading provider of products and services to the Life Science industry. We are focused on improving our customers’ performance across the manufacturing enterprise through the application of innovative technologies. ATS is embedded in numerous world leading Life Science multinational companies where we continue to deliver superior solutions. One of our …