Regulatory Affairs Consultant, CMC – Biologics

My research opens up new medical possibilities. And I do it Search Jobs Search Jobs Keyword Matching job links will appear below as you type. Location: When autocomplete results are available use up and down arrows to review and enter to select. Touch device users, explore by touch or with swipe gestures. Radius: Enter distance 5 15 25 35 50 Unit MILES KM View Remote Jobs View All Jobs View remote jobs View all jobs Regulatory Affairs Consultant, CMC – Biologics Primary Location: United States, Remote Job ID R0000047529 Category Regulatory / Consulting Apply Now About This Role About Parexel Parexel is a leading global clinical development partner delivering insights-driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere. We work with focus, agility, and shared purpose. We move with urgency to address patient needs and accelerate the delivery of new therapies. We embrace bold thinking, adapt quickly to change, and continually raise the bar for the speed and quality of clinical research. We are expanding our team and seeking talented individuals to help drive industry-leading innovation, With Heart®. About The Role We are seeking a Regulatory Affairs Consultant, CMC – Biologics to join our team in a remote capacity based. As a Regulatory Affairs Consultant, CMC- Biologics, you will provide CMC regulatory strategy input and expertise for investigational, new, and marketed biologic and small molecule drug products. Your work will help ensure these products are developed and maintained in compliance with global regulatory requirements and guidance, with primary responsibility for the US, EU, and Canada to support smooth, timely approvals and continued marketing. This position plays a key role in regulatory compliance, the preparation of CMC and GMP documentation for health authority submissions, and support for health authority CMC meetings. You will collaborate with Regulatory Affairs leads and cross-functional partners across manufacturing, quality, Technical Operations, affiliates, and external partners, and contribute to regulatory strategy from early development through post-approval changes. Responsibilities include preparing and reviewing CMC and GMP-related submissions, representing CMC Regulatory Affairs in project team meetings, and supporting monthly global CMC GRT meetings, with opportunities to deepen your expertise and influence program outcomes. You will join a fast-paced, growth-oriented environment focused on making a meaningful impact through strategic CMC regulatory input, high-quality submissions, and continuous improvement of departmental processes. Your work helps bring safe, high-quality medicines to patients, which is central to advancing clinical research. With diverse, global teams and continuous learning opportunities, you can explore career paths and expand skills across regulatory affairs and drug development.

Key Responsibilities

Support Regulatory Affairs leads in developing CMC regulatory strategies and contingency plans for biologic and small molecule drug substances, drug products, and drug-device combination products. Support the development of CMC regulatory strategies for development-phase products, from early development through marketing applications, and for post-approval changes to marketed products. Determine regulatory and scientific and technical requirements for CMC and GMP-related submissions and inquiries. Prepare, coordinate, and review CMC and GMP-related documents for submission to regulatory authorities, ensuring compliance with regulatory requirements, company standards, and scientific and technical requirements. Support Regulatory Affairs leads in representing CMC Regulatory Affairs in project team meetings, providing regulatory guidance and perspective to cross-functional teams in conjunction with global regulatory leads. Support Regulatory Affairs leads in preparing for health authority CMC meetings, including mock meetings and meeting planning. Support monthly CMC GRT meetings with global cross-functional teams for assigned products. Interact with manufacturing and quality groups, partner organizations, and other stakeholders on CMC issues. Develop and maintain collaborative relationships with local and global functional units, including CMC Regulatory Affairs, manufacturing sites, Quality, Technical Operations, affiliates, external partner companies, contract manufacturers, packagers, and suppliers. Prepare departmental job procedures. Assess and develop innovative ideas to optimize local and global CMC Regulatory Affairs departmental processes, improving efficiencies and addressing current and future challenges. Candidate Profile You Will Thrive In This Role If You Bring Strengths in proactive strategic thinking, analytical problem solving, and negotiation Experience working in the pharmaceutical industry within a regulated environment Strong collaborative, communication, and presentation skills, with the ability to lead meetings and work effectively in a matrixed environment and across cultural lines An operationally minded approach, with the ability to prepare high-quality technical documents and submissions using internal systems The ability to independently manage and prioritize a multi-project workload Proficiency with document management and regulatory information systems, Trackwise Digital, and TRS Viewer

Required Qualifications

Bachelor's degree in Pharmaceutical Sciences or Chemistry, or a Pharm.D. 4-6 years of CMC experience in the pharmaceutical industry, with a history of successfully preparing regulatory filing documentation Comprehensive knowledge of the drug development process, pharmaceutical technology, drug manufacturing processes, GMP, and related issues Knowledge of CMC regulatory requirements for biologics and small molecules during development and post-approval, including biologic upstream and downstream processes, analytical methods, and drug-device combination products Comprehensive knowledge and experience preparing CMC (Quality) sections for investigational and marketed product submissions (IND, NDA, DMF) for the FDA and equivalent submissions for Europe and Canada Comprehensive understanding of the global regulatory environment Demonstrated experience with the Microsoft suite of programs (Word, Excel, PowerPoint, and Outlook) Strong analytical, problem-solving, organizational, and negotiation skills

Preferred Qualifications

Master's or Ph.D. degree, preferably in Pharmaceutics, Biochemistry, Molecular Biology, Biotechnology, or Biology Regulatory Affairs Certification (RAC) Experience in CPP application filing through eCATS and 510(j)(3) reporting through nextGen portals

Benefits

And Compensation Health, Vision & Dental Insurance Tuition Reimbursement Vacation/Holiday/Sick Time Flexible Spending & Health Savings Accounts Work/Life Balance 401(k) with Company match Pet Insurance For a complete list of benefits, please visit www.parexel.com/us-benefits (opens in new window). Parexel offers competitive salaries based on several factors, including the position and level offered, skills, education, training, experience, professional achievements, and location. Some roles may also be eligible for additional incentives, bonuses, or other compensation programs. Our Talent Acquisition team will provide details on applicable bonus plans or incentive structures for eligible positions. If this job doesn't sound like the next step in your career, but perhaps you know of someone who'd be a perfect fit, send them the link to apply! We believe in flexibility, growth, and creating space for people to do their best work. Join us and be part of a team where your contributions help shape the future of clinical research. EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the United States includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status. Apply Now Share this Page X (opens in new window) Facebook (opens in new window) LinkedIn (opens in new window) Email (opens in new window) New Medicines, Novel Insights Newsletter Parexel's insight-generation engine, our people, share perspectives on patient-guided clinical research. Learn more Benefits & Support At Parexel, we prioritize putting people first, allowing you to achieve your best work. Explore the Flexible Work Program, our "Bravo" Recognition Program, and how we build our well-being in our supportive culture. Learn more Our work culture Learn about our culture, perks, learning opportunities, and our corporate responsibility approach. Parexel's compassionate and results-driven work culture prioritizes patient care and employee growth. Learn more Inclusion at Parexel Learn how Parexel celebrates the differences our workforce and patients bring and ensures an inclusive environment. Learn more Parexel’s hiring process It’s all about finding the right fit, for you and for us. Our recruiters work with you and our hiring managers to bring together a team and culture where everyone can grow and be successful. Learn more Working where it works for you Parexel offers a flexible approach to work that meets your personal needs while maintaining quality delivery for patients. Choose the right work arrangement for you - in-office, home-based or a mix. Learn more JOBS FOR YOU Senior Regulatory Affairs Consultant, CMC – Post-Approval Vaccines United States of America, Remote Regulatory Affairs Consultant, CMC – Biologics United States of America, Remote Manager, Central Monitoring - FSP Argentina, Remote View All Jobs There is no jobs to view You currently have no saved jobs to view. Make sure to accept the Functional cookies to enable this module to display saved job links. You will be able to review them here when you revisit this page.. View Open Positions More Than A Job

Benefits

Benefits vary by country, but Parexel is passionate about our team’s overall wellness. Learn More Career Advancement We believe that investing in your professional and personal development is an investment in Parexel, and we want to help you realize your full potential and career. Learn More