Clinical Trial Associate

The Clinical Trial Associate is responsible for providing logistical support for one or more early phase clinical studies.
Primary Accountabilities and Responsibilities:
- Provide logistical support for Study Team
- Develop, maintain and manage appropriate study documentation
- Collect, review and approve regulatory documents from clinical sites
- Initiate, maintain and reconcile Trial Master File
- Set up and maintain tracking systems and tools and report study metrics to support the clinical study
- Coordinate communication of tracking information within Study Team and to sites
- Manage and track clinical and non-clinical supplies
- Manage and track study-specific payments
- Coordinate investigator meeting planning in concert with travel planners, including preparing meeting materials and on-site meeting implementation (as requested)
- Develop study related documents in collaboration with the study team

Experience:
- 2+ years industry experience in equivalent role
- Performs job duties independently with minimal supervision and guidance
- Self-motivated and displays initiative
- Highly effective verbal and written communication skills in English
- Effectively collaborates with team members
- Proven organizational skills demonstrated by the ability to understand and prioritize instructions and deliver on time
- Experience using computer applications including spreadsheets, email, word-processing software & web-based systems

Education:
Bachelors degree or equivalent undergraduate degree required (scientific or healthcare discipline preferred)

- Working knowledge of international regulatory and ICH GCP guidelinesTo find out more about Real Staffing please visit www.realstaffing.com