Site Activation Specialist Assigned To Client Mexico, Chile, Colombia, Brazil, Argentina

1 semana atrás


São Paulo, São Paulo, Brasil Syneos Health, Inc. Tempo inteiro

Site Activation Specialist assigned to client Mexico, Chile, Colombia, Brazil, ArgentinaDescriptionSyneos 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 on the customer and the patient.
We continuously seek ways to simplify and streamline our work to make Syneos Health easier to work with and for.Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals.
We are agile and driven to accelerate the delivery of therapies because we are passionate about changing lives.Discover what our 29,000 employees across 110 countries already know:WORK HERE MATTERS EVERYWHEREWhy Syneos HealthWe are passionate about developing our people through career development, support, training, peer recognition, and rewards.We are committed to our Total Self culture — where you can be authentic.
We care for our people and foster diversity of thoughts, backgrounds, and perspectives.Job ResponsibilitiesResponsible for functions at the country level, including:Local Submissions Specialist — following project direction, serving as a point of contact during start-up, compiling/reviewing documentation for site activation.Preparing and submitting regulatory and ethics applications, amendments, and notifications under supervision.Acting as liaison between investigational sites and functional leads, overseeing site activation end-to-end.Supporting site ID and feasibility assessments.Assisting with investigator contract and budget negotiations, quality control, and document archiving.Qualifications include an Associate's Degree or equivalent, understanding of clinical trial processes, organizational skills, effective communication, independence, teamwork, problem-solving, and computer proficiency.This posting is for a potential future opportunity; expressing interest will add you to our talent pipeline for consideration.Discover more about us at InformationTasks and responsibilities are not exhaustive.
We may assign additional duties at our discretion.
We consider equivalent experience and skills, and nothing herein creates an employment contract.
We are committed to compliance with applicable laws and providing accommodations as needed.SummaryResponsible for quality deliverables at the country level, following project timelines, tracking milestones, and ensuring documentation compliance.
Working within SOPs, maintaining training records, and submitting documents to TMF are also key responsibilities.Work here matters everywhere.
Join us and help deliver therapies to those who need them most, contributing to a meaningful career that improves lives worldwide.
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