Description
Responsibilities:- Provide assistance to clinic staff by organizing files, projects, data, etc.
- Provide general office management to keep operations running smoothly.
- Assist with the development and execution of clinical research studies and programs
- Work under specific instructions to assist with routine tests, experiments, and procedures
- Collect, process, and assist in the compilation and verification of research data, samples, and/or specimens (following strict protocol and detailed instructions)
- Enter data from forms and documents into databases and other documents
- Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol
Perform literature searches, research, and overall administrative assistance - Follow established policies, procedures, and objectives, continuous quality improvement objectives, and safety, environmental, and infection control standards.
- Perform other duties as assigned
Knowledge, Skill and Competency Requirements:
- Excellent oral and written communication skills, interpersonal relationship skills, knowledge GCPs and regulations relating to clinical research.
- Must have a working knowledge of computer technology and its application to the clinical environment.
Must be able to anticipate obstacles and proactively develop solutions to achieve project goals. - Must have a general understanding of functional issues and routine project goals from an organizational perspective.
Education/Experience:
- CRA I
- Must have a minimum of a Bachelors Degree. This position requires a minimum of two years working CRA or equivalent in a pharmaceutical or biotech environment.
To find out more about Real please visit www.realstaffing.com