About this role
Sr Regulatory Consultant - LATAM (Biologics & CTA exp Must have)
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
The Chemistry Manufacturing Controls Manager will support the execution of multi-product global regulatory CMC for marketed products. This role contributes to the preparation and submission of regulatory CMC documentation and provides regulatory support to various cross functional teams.
Key Duties and Responsibilities
- Execute commercial Lifecycle Management (LCM) strategy and submissions with a focus on US/CA/EU.
- Reviews CMC sections of regulatory submissions, as well as the interactions and responses with regulatory agencies
- Works with regulatory colleagues in development of global regulatory CMC strategies and Submissions
- Participates effectively on cross-functional teams and may serve as the primary regulatory CMC contact for assigned products and projects
Required
Education
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Level & Experience
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Bachelor's degree, with a preference in Biology, Chemistry, Pharmacy, Regulatory Affairs for Drugs, Biologics or Medical Devices, or another related life-science field
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Typically requires 4 years of experience in the pharmaceutical industry or related field, or the equivalent combination of education and experience
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Preferred experience supporting Small Molecule programs
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Required Knowledge/Skills
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Strong interpersonal skills to exchange complex information with others and to guide others
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Proficiency in regulatory (FDA, EMA, Health Canada and ICH) guidelines
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Strong problem-solving skills
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Ability to collaborate and communicate in an open, clear, complete, timely and consistent manner
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Strong sense of planning and prioritization, and the ability to work with all levels of management
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Sound knowledge of cGMP, FDA, EMA, ICH
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Get to know Syneos Health
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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.
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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.
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Summary
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Regulatory Submission manager overseeing the submission plans for various products in development and on market products in US/ EU/ and global markets.