Proposal and SOW Development (30-40%) : - Understand and share proposal requirements thoroughly. - Work with multiple internal stakeholders to develop proposal content in line with RFP/RFI. - Summarize and prepare (with support of internal stakeholders) key
Description : About us We are Digital Science and we are advancing the research ecosystem. We are a pioneering technology company, and our vision is of a future where a trusted and collaborative research ecosystem drives
Medical Oversight : - Provide clarity on general protocol questions, and medical guidance for protocols as required. - Serve as medical expert providing guidance on patient eligibility, and investigational product related questions. - Document contacts in
JOB SUMMARY : Responsible for leading, planning and execution of all data management activities for assigned projects, ensuring focus on data integrity, validity, reliability in accordance with standard processes, sponsor guidelines, industry best practices and regulatory
The Vendor Manager (VM) is responsible for establishing and managing project supplier and vendor scope, timelines, and costs for awarded opportunities throughout the project life cycle, including the execution of work orders and change orders. Additionally,
The Project Assistant works with Project Managers, Project Coordinators and Clinical Research Associates (CRA) at many stages during clinical studies. Works independently to coordinate and manage study deliverables and administrative tasks, as required by the project
The Strategist, Patient Recruitment & Site engagement works with the Associate Director, Patient recruitment strategies and Development and the Specialist, Multimedia & Recruitment in supporting patient recruitment strategies and site engagement. This role will be perfect
The Senior Regulatory Affairs Specialist will provide leadership for assigned projects regarding all regulatory activities that lead to startup of clinical trials and will oversee global/multinational complex large clinical trial submissions. This role will be responsible for sponsor-facing
Description Principal / Senior Medical Writer - with proven strong clinical document writing experience Principal / Senior Medical Writer - with proven strong clinical document writing experience Syneos Health® is a leading fully-integrated life sciences services
The Senior Statistical Programmer will lead single and/or multiple clinical trials and be responsible for the development, maintenance, and validation of annotated Case Report Forms (aCRFs) as well as of specifications and statistical programming of Standard Data Tabulation