Cra Ii (Multi-Sponsor) - Argentina Home Based (Pilar)

Cra Ii (Multi-Sponsor) - Argentina Home Based (Pilar)

OverviewCRA II (Multi-sponsor) - Argentina Home Based.
Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.
We translate clinical, medical affairs and commercial insights into outcomes to address modern market realities.
Our Clinical Development model places the customer and patient at the center of everything we do.
Whether you join us in a Functional Service Provider partnership or a Full-Service environment,



you'll collaborate with passionate problem solvers to help our customers achieve their goals.WORK HERE MATTERS EVERYWHEREResponsibilitiesConduct 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 forms.Develop and implement tools, procedures, and processes to ensure quality monitoring, such as creating monitoring plans, checklists, and templates.Contribute to the design, implementation, and delivery of processes, programs, and policies, including developing standard operating procedures (SOPs) and training materials.Manage defined components of projects or processes within the area of responsibility, such as coordinating site visits, tracking study progress, and resolving issues.Ensure accurate and timely documentation of monitoring activities and findings, including writing monitoring reports, follow-up letters, and action plans.Collaborate with cross-functional teams to support clinical trial operations, including working with investigators, site staff,



and other stakeholders to ensure smooth study conduct.QualificationsBachelor's degree in a related field or equivalent experience.Minimum of 2-4 years of experience in clinical research monitoring.Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.Excellent communication and interpersonal skills; ability to work independently and manage multiple priorities.Proficiency in using clinical trial management systems and other relevant software.CertificationsCertified Clinical Research Associate (CCRA) or equivalent certification preferred.Necessary SkillsAttention to detail and strong analytical skills.Problem-solving abilities and critical thinking.Ability to work effectively in a team environment.Strong organizational and time management skills.Proficiency in Microsoft Office Suite.Additional InformationSummary: Roles within Clinical Monitoring/CRA job family at the P21 level are responsible for ensuring that clinical research studies are conducted in accordance with widely accepted clinical practices.




This includes conducting on-site and remote monitoring, developing tools, procedures, and processes, and providing support in design and delivery of processes, programs, and policies.
This is an individual contributor role with potential supervisory responsibilities and a focus on quality and integrity of clinical trials.Seniority level: Mid-Senior levelEmployment type: Full-timeJob function: Research, Analyst, and Information TechnologyFor location: Buenos Aires, Buenos Aires Province, Argentina
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📌 Cra Ii (Multi-Sponsor) - Argentina Home Based (Pilar)
🏢 Syneos Health
📍 Pilar