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PA

Parexel

via Workday

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CMC Regulatory Affairs Consultant with experience in peptides and oligonucleotides

Anywhere
Full-time
Posted 2/1/2026
Verified Source
Key Skills:
Analytical chemistry
Regulatory strategy
CMC documentation

Compensation

Salary Range

$120K - 200K a year

Responsibilities

Lead global regulatory CMC strategy for peptide and oligonucleotide therapeutics, ensuring compliance and facilitating product approvals.

Requirements

Requires 4-7 years of experience in peptide or oligonucleotide synthesis, analytical testing, and regulatory submissions, with proficiency in chromatography, LC-MS, NMR, and knowledge of FDA/ICH/USP standards.

Full Description

Exceptional opportunity for a highly experienced analytical chemist to partner with a large global biopharmaceutical client and lead regulatory CMC strategy for cutting‑edge peptide and oligonucleotide therapeutics. In this role, the Regulatory Affairs Senior/Consultant will drive global regulatory strategy and submission activities for complex synthetic and nucleic acid–based products, partnering closely with R&D, CMC, clinical, and quality teams to ensure compliance with international standards and accelerate successful product approvals. Qualifications & Experience • Educational Background • Bachelor’s or Master’s degree in chemistry, biochemistry, pharmaceutical sciences, or related discipline. Ph.D. in organic chemistry is preferred if possible. • Technical & Regulatory Expertise • 4-7 years in peptide or oligonucleotide synthesis, purification, and analytical testing (HPLC, LC-MS, NMR). • Hands-on experience with solid-phase synthesis or phosphoramidite-based workflows. • Familiarity with purity, identity, sequence confirmation, and impurity profiling requirements per FDA/ICH/USP standards. • Regulatory & Professional Competencies • Strong understanding of regulatory requirements for synthetic peptides and oligonucleotides and ability to analyze guidelines and precedents. • Proven track record preparing CMC documents and regulatory submissions. • Analytical, well-organized, and able to work across functions to resolve technical or compliance issues. Desired Skills • Technical Skills • Proficiency in chromatography (HPLC/UPLC), LC-MS, UV‑Vis, NMR, and sequence confirmation tools. • Experience with automated or scale‑up synthesis platforms, lab instruments, and LIMS/electronic lab notebooks. • Preferred Qualifications • Experience with conjugation strategies (e.g., peptide-oligo, ligand-oligo constructs). • Knowledge of global regulations (FDA, EMA, ICH) for biologics and oligo therapeutics. • Process development or GMP exposure in peptide/oligo manufacturing settings. Based upon the location of this client partner, candidates located in EST are preferred. Consideration, however, will be given to exceptional candidates in other time zones located in the US and Canada. #LI-LB1 #LI-REMOTE

This job posting was last updated on 2/8/2026

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