Overview
cra ii or sr cra assigned to client mexico, chile, brazil, argentina
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 brings the customer and the patient to the center of everything that we do. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: work here matters everywhere.
job responsibilities
* conduct 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 participating in the development of 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
qualifications
* bachelor'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
certifications
* certified clinical research associate (ccra) or equivalent certification preferred
necessary skills
* attention 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 information
tasks, duties, and responsibilities as listed in this job description are not exhaustive. The company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the job description. The company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing herein should be construed to create an employment contract. The company is committed to compliance with the americans with disabilities act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
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