Clinical Trial Regulatory Advisor - The position is to work with submissions in Canada - Argentina Home Based

Syneos Health, Inc.; Argentina; Remoto; ARS 92.983.000 - 139.474.000; Tempo integral

Resumo da vaga

Syneos Health, Inc. is seeking a Clinical Trial Regulatory Advisor to support submissions for Canada from Argentina in a home-based role. You will oversee core regulatory documents, ensure timelines and quality standards, and drive submission strategy with project teams.

The ideal candidate has knowledge of GxP (GCP, GVP, ISO 14155), excellent English communication, and strong documentation and presentation skills. Proficiency with Microsoft Office and web-based systems is required.

Qualificações

• Minimum BA/BS preferred.
• Knowledge of GxP (GCP, GVP, ISO 14155) and regulatory processes.
• Excellent written and spoken English with strong communication skills.

Responsabilidades

• Review and finalization of core regulatory documents for site initiation and study end submissions.
• Develop and support regulatory submission strategy and timeline adherence.
• Lead regulatory delivery on project activities to satisfy client requirements.
• Contribute to technical components of regulatory submissions (e.g., EU CTR Part I/II).
• Coordinate with agency interactions as needed.
• Ensure compliance with relevant quality standards and policies.

Conhecimentos

English proficiency

Presentation skills

Interpersonal skills

Teamwork

Formação

BA/BS preferred

Ferramentas

Microsoft Office

Web-based systems

Email

Descrição da vaga

Clinical Trial Regulatory Advisor - The position is to work with submissions in Canada - Argentina Home Based

Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.
Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.
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 deliver – for one another, our customers, and, most importantly, for those in need.
Discover what your 25,000 future colleagues already know:

• 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 building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life.
• We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.
  

Job Responsibilities

Provides regulatory and technical support for assigned Regulatory work: review and finalization of essential core documents required for site initiation regulatory and core submissions performance (if applicable) from site startup until study end related submissions. Accountable core regulatory activities; including the agreed regulatory submission strategy and ensures tasks are undertaken in accordance with agreed timelines, allocated budgets, and required quality standards.

Responsibilities:

• Perform the CTRA operations deliveries on specific project activities which may include in particular regulatory leading function which result in client satisfaction.
• Review clinical trial study core documents (such as labelling for regulatory compliance etc.)
• Contribute to and prepare the technical components of a regulatory core submission (such as EU Clinical Trial Regulation Part I and/or II) Contribute to or support with any agency interactions.
• Manage and/or operationalize the delivery of day-today regulatory activities for assigned project according to agreed timelines, scope of contract, budgets, and strategies.
• Act as a subject matter expert and help the team members with day-to-day trouble shooting activities, presenting solutions to project related problems.
• Participate as regulatory support on multidisciplinary project teams, which may include clinical and other technical experts, to develop products throughout their life cycle.
• Identifies and reports on areas of process and risk.
• Ensure personal compliance and/or accuracy with relevant quality standards. Consistently achieve and maintain utilization target and departmental goals.
• Maintains current knowledge of applicable regulations and guidelines. Identify relevant laws, regulations, and guidance documents covering pre and/or post-market requirements for healthcare products.
• Responsible for performing activities that are in compliance with applicable Corporate and Divisional Policies, Standard Operating Procedures and Operating Guidelines and performing other duties as assigned by management.
  

Qualifications:

• Minimum of a BA or BS preferred
• Experience in working to applicable GxPs (e.g. GVP, GCP, ISO 14155) etc
• Excellent presentation, documentation, influencing, and interpersonal skills (both written and spoken English) as well as a team-oriented approach.
• Proficient computer skills in Microsoft Office Suite, web-based systems, voicemail, Email and Internet are necessary.

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 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.

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.

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.

http://www.syneoshealth.com

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 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.