Description
Responsibilities:- Participates in the design, planning, implementation and overall direction of clinical research projects; May co-ordinate the activities of relevant colleagues within the company and investigators to ensure compliance with the overall scientific study objectives.
- Travels to field sites to monitor studies.
- Reviews study protocols, reports and manuscripts. Contribute technical and clinical operations expertise for these documents.
- Works with Data Management and Biostatistical staff on the design of documents and processes for the collection of study data from participating sites.
- Ensures accurate and complete study management/data collection and transfer into the data management system.
- Ensures site compliance with regulations and study protocol.
- Assists, prepares and manages study timelines.
- Participates in Project Team Meetings.
- Keeps informed of trends and developments in clinical research.
- Analyzes alternative approaches to solve problems or devleop new perspectives on existing solutons.
Education Requirement: B.S. or M.S. in Biology, Chemistry, Molecular Biology or related discipline.
Skills / Experience: Requires 2-6 years relevant work experience, however, 4-6 years preferred. Must be a self starter, able to work in a team situation, have the ability to solve problems in a detailed, comprehensive manner, demonstrate urgency and energy to handle problems, meet timelines and manage sites. Requires excellent lab skills and experience is Microsoft Office applications.
To find out more about Real please visit www.realstaffing.com