Clinical Research Assistant II (Contract) - On Call - 6-8 weeks

About the role

Performs daily clinic tasks to assist coordinators with study procedures and administrative duties in support of clinical studies, following Good Clinical Practice (GCP) guidelines, applicable regulations, standard operating procedures (SOP), and work instructions.

Responsibilities

• Assist with study procedures such as Electronic Self-Assessment Questionnaire (ESAQ) administrations, check-in process, informed consent signing, instrumentation assist, and photography assist.
• Perform administrative tasks including test material preparation, making appointment reminders, and quality checking (QC) study documents.
• Assist in the development of study paperwork for coordinators.
• Report to clinic on-time for all assigned studies.
• Perform tasks for other departments as needed.
• Provide excellent customer service to clients and panelists, maintaining positive and respectful interactions with peers and leadership.
• Comply with safety and Operational Integrity procedures and processes.

Requirements

• Associate’s degree or at least one year of administrative/clerical work experience.
• CCRC/CCRA certification is a strong plus.
• Strong attention to detail and organizational, verbal, and written communication skills.
• Able to follow instructions and study protocols according to GCP guidelines, applicable regulations, and SOPs.
• Able to lift moderately heavy items.
• Ability to manage and coordinate multiple projects in a fast-paced, highly professional environment.
• Must be flexible to work morning/afternoon shifts.