Job Summary
The role entails leading and managing regional operational functions for clinical studies. This includes oversight of site management, monitoring teams, adherence to study timelines, and ensuring quality and deliverables are met effectively.
Responsibilities
- Direct the implementation of studies and manage communications across teams.
- Monitor site performance and ensure accurate safety reporting.
- Oversee the management of study documentation and necessary supplies.
- Identify potential risks and recommend improvements to existing processes.
Qualifications
- A bachelor’s degree in a science-related field is mandatory; a master’s degree in a related field is preferred.
- 4–6 years of pertinent experience in clinical research is required.
- A minimum of 1–3 years in roles such as CRA or clinical operations coordinator is essential.
- Comprehensive knowledge of clinical research operations, including ICH guidelines and local regulations.
- Strong capabilities in communication, organization, analytical reasoning, prioritization, and collaboration.
Emmes Group provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
