Sr Cra - Sponsor Dedicated - Argentina Home Based (Santa Fe)

Sr Cra - Sponsor Dedicated - Argentina Home Based (Santa Fe)

13 oct
|
7257 Syneos Health Argentina
|
Santa Fe

13 oct

7257 Syneos Health Argentina

Santa Fe

Sr CRA - Sponsor dedicated - Argentina Home Based 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 brings the customer and the patient to the center of everything that we do.
We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work 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 to change lives.
Discover what our 29,000 employees, across 110 countries already know: WORK HERE MATTERS EVERYWHERE Why Syneos Health We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
We are committed to our Total Self culture - where you can authentically be yourself.
Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
We are continuously building the company we all want to work for and our customers want to work with.
Why?
Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives - we're able to create a place where everyone feels like they belong.Job ResponsibilitiesConduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices, including reviewing study protocols, case report forms, and regulatory documentsDevelop tools, procedures, and processes to ensure quality monitoring, such as creating monitoring plans, checklists, and standard operating proceduresContribute to the design, implementation, and delivery of processes, programs, and policies by providing expert input and feedback during development and review stagesDirect the work of lower-level professionals or manage processes and programs, including training and mentoring junior staff and overseeing their monitoring activitiesEnsure trials are conducted in accordance with regulatory requirements and company standards by performing regular audits and inspections, and addressing any compliance issues that ariseProvide guidance and support to clinical research teams, including answering questions, resolving issues,



and facilitating communication between team members and stakeholdersMaintain accurate and timely documentation of monitoring activities, including writing detailed monitoring reports, tracking study progress, and updating databasesIdentify and resolve issues related to clinical trial conduct, such as protocol deviations, data discrepancies, and adverse events, and implement corrective and preventive actions as neededCollaborate with cross-functional teams to ensure successful trial execution, including working with project managers, data managers, biostatisticians, and regulatory affairs specialistsQualificationsBachelor's degree in a related fieldMinimum of 5 years of experience in clinical research monitoring; this role is a progression within the level from a Sr CRA IIn-depth knowledge of clinical trial processes and regulationsStrong analytical and problem-solving skillsExcellent communication and interpersonal skillsAbility to work independently and as part of a teamCertifications: Certified Clinical Research Associate (CCRA) or equivalent certification preferredNecessary SkillsProficiency in clinical trial management systems and softwareAbility to manage multiple projects and prioritiesStrong attention to detail and organizational skillsAbility to travel as required for on-site monitoringKnowledge of Good Clinical Practice (GCP) guidelines and regulatory requirementsGet to know Syneos HealthOver 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.
No matter what your role is, you'll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment.
Learn more about Syneos Health.
InformationTasks, 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 contained herein should be construed to create an employment contract.
Occasionally, required skills/experiences for jobs are expressed in brief terms.
Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees.
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.
Discover what our Syneos Health colleagues already know: work here matters everywhere.
Work alongside the brightest minds in the biopharmaceutical industry taking down walls and removing barriers to speed our customers' delivery of important therapies to patients.
We are strategic thinkers who actively seek different perspectives, whether across offices or across oceans.
Because we solve some of the toughest challenges facing the most prestigious healthcare companies today, you'll gain exposure and be supported with comprehensive resources including emerging technologies, data, science and knowledge sharing.
The diversification and breadth of Syneos Health creates a multitude of career paths and employment opportunities.
We're a growing, integral company dedicated to advancing our talent past their initial role.
Discover what our 29,000 employees already know: work here matters everywhere.
We work hard, and smart, all in the name of getting much-needed therapies to those who need them most.
A career with Syneos Health means your everyday work improves patients' lives around the world.
Selecting us as an employer secures a career in which you're guaranteed to: Partner with the most diverse team of experts in the industry.
From the top down, our people are inspiring.
Everyone has a voice and is encouraged to use it.
Work in specialized Syneos Health teams that are therapeutically or functionally aligned for expert collaboration.
We assemble clinical teams where everyone, from CRAs to senior management, is skilled in the same therapeutic area or customer teams.
With this structure, everyone on your team speaks the same language and can deliver unique insights into the therapeutic environment and patient population.
We are partners with purpose.
We integrate seamlessly with our customers and do what's best for their success.
Our people provide the brilliant ideas, valuable insights and endless energy that accelerates the impact of life changing therapies worldwide.
#J-*****-Ljbffr

📌 Sr Cra - Sponsor Dedicated - Argentina Home Based (Santa Fe)
🏢 7257 Syneos Health Argentina
📍 Santa Fe

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