Sr Regulatory Cmc Consultant - Small Molecule & Veeva Rim Must Have

Sr Regulatory CMC Consultant - Small Molecule & Veeva RIM Must Have (EMEA /US/Canada)
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
Required Knowledge/SkillsGood knowledge of North America regulatory affairs frameworkUnderstanding of requirements and processes to maintain a product on market, report, and surveillanceUnderstanding of drug development and related conceptsAbility to assess and understand regulatory guidelinesStrong written and verbal communication skillsAbility to work effectively within a team environmentAbility to plan, prioritize and contribute to work and projects in systematic and efficient mannerRequired Education Level & Experience
Bachelor's, Master's or PhD degree, with a preference in Biology, Chemistry, Pharmacy, Regulatory Affairs for Drugs, Biologics or Medical Devices, or another life-science fieldTypically requires 8 years of experience in the pharmaceutical or biotech industry or in a related field, or the equivalent combination of education and experienceGet 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. 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.Summary
General Position Summary Regulatory Strategy Manager will be responsible for overseeing the development of global regulatory strategy for development product(s) within the Vertex portfolio and contribute to the global regulatory strategy for the assigned program(s) including supporting clinical trial related activities. This role requires advanced understanding of regulatory affairs frameworks in the US, Europe, or other international markets, drug development, and related concepts, and the ability to translate this knowledge into effective regulatory planning and strategy development. Key Duties and ResponsibilitiesKey Duties and Responsibilities
Supports North America regulatory strategy under guidance of regional and global regulatory lead, as neededIdentifies regulatory requirements for submissions for North America, as neededManages process for preparation, submission and approval or regulatory applications within North America, as neededProvides technical regulatory input for key product development or registration documentsWorks to ensure compliance of regulatory submissions with current regulations and guidance
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