Observational Research Specialist

Working from our office location in Sao Paulo, as an Observational Research Specialist (ORS) you will Independently provide site management and support activities for Observational/ Non-interventional research study sites in accordance with relevant Standard Operating Procedures (SOPs), study-specific procedures and regulations. You will be responsible for supporting the development of the Clinical Operations service delivery within Parexel.

Depending on study assignment and with support as necessary key accountabilities can include acting as the primary contact for assigned, site identification, selection and start-up activities including negotiation of site agreements and budgets. customization of country/site specific documentation and conduct remote and on-site monitoring activities through all study stages.

To be considered for this opportunity you must have clinical trials experience with an understanding of clinical site process. Understanding of GCP and relevant regulations plus a university degree are expected. This is a virtual team environment and your strong interpersonal and communication skills will help you to succeed. Fluency in English is required.

QualificationsExperience in clinical trials ideally in monitoring Solid understanding of Observational/ Non-interventional research methodology and terminology. University degree (biological science, pharmacy or other health-related discipline preferred) Fluency in English is required