Cra Ii Or Sr Cra (Home-Based - Chile / Argentina)

OverviewCRA II or Sr CRA (Home-based - Chile / Argentina)Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.

We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.

Our Clinical Development model centers the patient and the customer, with a focus on simplifying and streamlining work to improve experiences for both teams and customers.

This role supports clinical trial monitoring activities in a home-based capacity for Chile or Argentina.ResponsibilitiesConduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices, including reviewing study protocols, informed consent forms, and case report formsDevelop and implement tools, procedures, and processes to ensure quality monitoring, such as creating monitoring plans, checklists, and templatesContribute to the design, implementation, and delivery of processes, programs, and policies, including participating in the development of standard operating procedures (SOPs) and training materialsManage defined components of projects or processes within the area of responsibility, such as coordinating site visits, tracking study progress, and resolving issuesEnsure accurate and timely documentation of monitoring activities and findings, including writing monitoring reports, follow-up letters, and action plansCollaborate with cross-functional teams to support clinical trial operations, including working with investigators, site staff, and other stakeholders to ensure smooth study conductQualificationsBachelor's degree in a related field or equivalent experienceMinimum of 2-4 years of experience in clinical research monitoringStrong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirementsExcellent communication and interpersonal skillsAbility to work independently and manage multiple prioritiesProficiency in using clinical trial management systems and other relevant softwareCertificationsCertified Clinical Research Associate (CCRA) or equivalent certification preferredNecessary SkillsAttention to detail and strong analytical skillsProblem-solving abilities and critical thinkingAbility to work effectively in a team environmentStrong organizational and time management skillsProficiency in Microsoft Office SuiteWe are always excited to connect with great talent.

This posting is intended for an upcoming opportunity rather than a live role.

By expressing your interest, you\'ll be added to our talent pipeline and considered should this role become available.Get to know Syneos Health : Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.

Learn more at the Syneos Health website.

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