Clinical Research Assistant II
Job Description
Performs daily clinic tasks to assist coordinators with study procedures. Tasks may include but are not limited to Electronic Self-Assessment Questionnaire (ESAQ) administrations, check-in process, informed consent signing, instrumentation assist, photography assist, etc.
Performs daily administrative tasks to assist coordinators in study preparation and conduct. Tasks may include but are not limited to test material preparation, making appointment reminders, quality checking (QC) study documents, etc.
May assists in the development of study paperwork for coordinators
Reports to clinic on-time for all studies assigned to work
Performs tasks according to Good Clinical Practice (GCP) guidelines, applicable regulations, standard operation procedures (SOP), and work instructions
May perform tasks for other departments, as needed
Provides excellent customer service to clients and panelists, and maintains positive and respectful interaction with peers and leadership
Complies with and understands safety and Operational Integrity procedures and processes
Qualifications
- Associates degree or at least one year of administrative/clerical work experience
- CCRC/CCRA certification a strong plus
- Strong attention to detail and organizational, verbal and written communication and interpersonal skills
- Able to follow instructions and study protocols according to GCP guidelines, applicable regulations, and SOPs
- Able to lift moderately heavy items
- Able to manage and coordinate multiple projects in a fast-paced, highly professional environment
Additional Information
SGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, color, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression, genetics, status as a protected veteran, or any other characteristics protected by law.