CMC Regulatory Affairs Senior/Consultant - Small Molecules

Parexel; Carson City (NV); Remote; USD 90,000 - 130,000; Full time

Job summary

A global leading health consultancy is seeking an experienced CMC Regulatory Affairs Senior/Consultant to provide regulatory strategy for small molecule products. This role involves preparing regulatory documentation, collaborating with cross-functional teams, and ensuring compliance with global regulatory requirements. Ideal candidates will have a background in pharmaceutical sciences and demonstrate strong analytical and problem-solving skills. Preference for candidates in the Eastern Time Zone, but exceptional candidates from other zones may be considered.

Qualifications

• 4–6 years of CMC regulatory experience for Consultant level, 7+ years for Senior Consultant.
• Proven success in preparing regulatory documentation for FDA, EMA, and Health Canada.
• In-depth understanding of drug development, manufacturing processes, and GMP.

Responsibilities

• Provide regulatory strategy input for small molecules.
• Prepare, coordinate, and review CMC and GMP-related documents.
• Partner with manufacturing and quality to address CMC-related issues.

Skills

Regulatory strategy input

Excellent analytical skills

Strong problem-solving abilities

Proficiency in Microsoft Office Suite

Education

Bachelor's degree in Pharmaceutical Sciences, Chemistry, or related field

Advanced degrees (Pharm.D., M.S., Ph.D.) preferred

Tools

CREDO

Trackwise Digital

Job description

Overview

Exciting opportunity for an experienced and highly motivated professional to join our Global Regulatory Affairs team as a CMC Regulatory Affairs Senior/Consultant. This role is critical to ensure our client’s investigational, new, and marketed small molecule products are developed and maintained in compliance with global regulatory requirements. The primary regions of responsibility include the United States, European Union, and Canada, with a focus on facilitating timely approvals and supporting continued market access.

Key Responsibilities

• Strategic CMC Leadership
  • Provide regulatory strategy input for small molecules (previous experience with biologics and/or drug-device combination products are a plus)
  • Support regulatory leads in developing contingency plans for CMC-related scenarios
  • Represent CMC Regulatory Affairs in cross-functional project meetings and provide regulatory guidance in collaboration with global regulatory leads
• Submission & Documentation Excellence
  • Prepare, coordinate, and review CMC and GMP-related documents for regulatory submissions
  • Develop CMC strategies for products across all phases—from early development to marketing applications and post-approval changes
• Cross-Functional Collaboration
  • Partner with manufacturing, quality, and external organizations to address CMC-related issues
  • Maintain collaborative relationships with internal stakeholders, affiliates, contract manufacturers, packagers, and suppliers
  • Support planning and execution of Health Authority meetings, including mock sessions
• Process Optimization & Innovation
  • Identify and implement process improvements to enhance regulatory efficiency and readiness
  • Participate in monthly CMC Global Regulatory Team meetings to align strategies across functions
  • Utilize regulatory systems and tools including CREDO, Trackwise Digital, and TRS Viewer
• Regulatory Systems & Reporting
  • Experience with CPP application filing via eCATS and 510(j)(3) reporting through nextGen portals is a plus
  • Ensure audit readiness and version control through meticulous documentation and system management

Qualifications

• Experience & Expertise
  • 4–6 years of CMC regulatory experience in the pharmaceutical industry for a Consultant level role, 7+ years for a Senior Consultant
  • Proven success in preparing regulatory documentation for FDA, EMA, and Health Canada (IND, NDA, DMF)
  • In-depth understanding of drug development, manufacturing processes, GMP, and regulatory frameworks for small molecules. Previous experience with biologics or combination device products are a plus!
• Skills & Attributes
  • Strategic and proactive mindset with strong operational execution
  • Excellent analytical, problem-solving, and negotiation skills
  • Effective communicator with strong interpersonal, presentation, and leadership abilities
  • Ability to manage multiple projects independently in a matrixed, multicultural environment
  • Proficiency in Microsoft Office Suite and regulatory systems
• Education
  • Bachelor’s degree in Pharmaceutical Sciences, Chemistry, or related field
  • Advanced degrees (Pharm.D., M.S., Ph.D.) in Pharmaceutics, Biochemistry, Molecular Biology, Biotechnology, or Biology preferred
  • RAC certification is a plus

Given the client's location, preference will be given to candidates residing in the Eastern Time Zone. However, exceptional individuals based other Time Zones will also be considered, provided they can accommodate the scheduling requirements of global meetings and calls as needed.

EEO Disclaimer

Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.