Regulatory Consultant (CMC-EU, GCC & AU)

Syneos Health, Inc.; United States; Remote; USD 120,000 - 180,000; Full time

Job summary

Syneos Health, Inc. is seeking a Regulatory Consultant (CMC-EU, GCC & AU) to lead CTD Module 3 sections, authoring and defending content in regulatory submissions.

The role requires experience with EU, US FDA, AU, GCC, and ROW regions and strong cross-functional collaboration with analytical, formulation, and manufacturing teams. You will manage day-to-day regulatory activities, prepare materials for regulatory meetings, and ensure compliance with global requirements.

Qualifications

• CTD Module 3 sections authored independently.
• Experience with post-approval variations and supplements.
• Ability to interpret data and defend content in authority queries.
• Ownership of CTD sections and knowledge of section numbers.

Responsibilities

• Conduct regulatory research to prepare submissions and regulatory plans.
• Prepare administrative and technical components of submissions for INDs, pre-approval packages, registrations, and post-approval maintenance.
• Manage day-to-day regulatory activities per timelines, budgets, and strategies.
• Participate as regulatory support on multidisciplinary project teams throughout product life cycle.
• Provide day-to-day troubleshooting and solution presentation to project-related issues.
• Prepare estimates for regulatory services as part of proposals.
• Support client meetings to discuss proposals and project status.

Skills

CMC authoring

CTD Module 3

Regulatory submissions

Cross-functional teams

CMC writing

Global regulatory knowledge

Job description

Regulatory Consultant (CMC-EU, GCC & AU)

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:

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 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

Mandatory Skillsets:

• CMC authoring exposure, authored CTD Module 3 (M3) sections independently.
• Anyone only compiling/reviewing documents will not fit.
• Experience with post-approval variations/supplements.
• Cross-functional interaction with analytical, formulation and manufacturing teams.
• CMC writing and lifecycle management for small molecules.
• Experience across: EU, USFDA, AU, GCC, ROW. (Not all)
• Candidate should:
  • Own CTD sections
  • Interpret technical data
  • Writes content from raw CMC documents
  • Defends content in authority queries
  • Knows section numbers and expectations

For non-complex and complex submissions, independently fulfill the following responsibilities:

• Conduct research of existing product data relative to global or regional regulatory requirements for the preparation of gap analyses, product development plans, and other regulatory submissions.
• Contribute to or prepare administrative and technical components of regulatory agency submissions for the IND, for pre-approval submission packages, for product registration applications, and for post-approval maintenance. Prepare briefing packages for regulatory agency meetings or scientific advice and contribute to or support the 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.
• Participate as regulatory support on multidisciplinary project teams, which may include clinical and other technical experts, to develop products throughout their life cycle.
• Act as a subject matter expert and help the team members with day-to-day trouble shooting activities, presenting solutions to project related problems.
• Prepare estimates for conducting regulatory services as part of single or multiple service proposals.
• Support meetings with clients to discuss proposals, the status of ongoing projects, and as part of general business development activities.
• Ensure compliance with appropriate global regulatory requirements and the company’s policies and processes.
• Prepare training materials and share best practices in the regulatory area, both internally and externally.
• Participate as regulatory support in internal or external project audits.
• Participate as regulatory support on internal cross-functional initiatives.
• Contribute to the creation and/or maintenance of SOPs and other process related documentation as required.
• Provide support in oversight to team members in the execution of their project responsibilities.
• Capable of identifying when to ensure line support required to provide additional guidance and direction.
• Maintenance of individual training records (Syneos Health or client related) and completion of all designated required training.

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.