Primary Duties And Responsibilities

• Understand and interpret clinical trial study protocols to design and develop calendars. Understand and interpret clinical trial agreements and sponsor budgets to develop site budgets for the protocol.

• Design and develop case report forms for clinical trial study protocols

• Develop a familiarity with Advarra’s Clinical Trial Management Software (CTMS) and Electronic Data Capture (EDC) software to utilize related functionalities in the design and development of calendars, budgets, financials and case report forms.

• Work closely with reporting manager to complete daily/ weekly calendars, budgets, financials and/or case report forms design to meet with pre-determined quality criteria.

• Understand and utilize internal case management software and other reporting software to ensure that daily/weekly work assignments are appropriately tracked and completed.

• Actively participate in team meetings and contribute meaningfully to discussions related to specific customer cases and/or protocols.

• Knowledge of clinical research methodology, industry regulations and Good Clinical Practice guidelines related to human research.

• Expected to work independently, as well as in a team environment.

• Good organizational and administrative abilities

• Familiarity with MS Office and various business software

• Preferred: 0-1 year work experience in job areas such as: o Clinical trial coordinator at site

• Clinical data management

• Pharmacovigilance

• Records management

• Highly personable nature that fosters teamwork

• Excellent communication skills – oral as well as written

• High energy and positive attitude towards working in a culturally diverse environment

• A passion for ensuring outstanding customer support with a solutions-oriented attitude.

• Proactive and takes ownership in all tasks from start-to-finish.