Regulatory Manager

Position: Regulatory Manager

Hourly Range: $80,000 - $120,000

Location: Baltimore, MD (On-site)

Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 locations in the US, UK, China, and Singapore, we support drug discovery through to manufacturing with fully integrated high-quality services.

We're proud of the impact we make and just last year, we supported 887 discovery projects
, 1,100+ CMC programs
, and 1,397 clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,300 global customers
. To learn more, visit

Pharmaron Clinical Pharmacology Center (CPC) is seeking an experienced Regulatory Manager or Senior Regulatory Manager to lead critical regulatory operations supporting Phase I through Phase IV clinical research studies. This is an exciting onsite opportunity for a regulatory professional who thrives in a fast-paced CRO environment and has deep expertise in IRB submissions, clinical trial regulatory documentation, Trial Master Files (TMF), and team leadership.

As the Regulatory Manager, you will serve as the regulatory subject matter expert and oversee regulatory activities from study startup through closeout. In this highly visible role, you will ensure regulatory compliance throughout the clinical trial lifecycle while mentoring and developing a team of regulatory professionals.

• Lead all regulatory activities throughout the clinical trial lifecycle, including IRB submissions, protocol amendments, informed consent updates, safety reporting, and study closeout submissions.
• Manage and maintain regulatory binders and electronic Trial Master Files (eTMF), ensuring essential documents are complete, compliant, and inspection-ready.
• Oversee study startup regulatory documentation and support sponsor, audit, and inspection readiness activities.
• Lead, mentor, and develop Regulatory team members while driving departmental performance, compliance, and continuous improvement.
• Serve as the primary regulatory liaison with Sponsors, IRBs, Clinical Operations, and Quality teams to support successful study execution and regulatory compliance.

• Bachelor's degree or equivalent combination of education, training, and experience.
• 5-10 years of clinical research regulatory experience.
• 5-10 years of hands-on experience managing IRB submissions and approvals.
• 5-10 years of experience managing essential documents for clinical trials.
• Strong working knowledge of:
  • ICH-GCP Guidelines
  • FDA regulations
  • 21 CFR Part 50 (Protection of Human Subjects)
  • 21 CFR Part 56 (Institutional Review Boards)
• Experience with electronic Trial Master File (eTMF) systems, including:
• Veeva Vault TMF and/or
• Florence eTMF
• Excellent written and verbal communication skills.
• Strong organizational, problem-solving, and project management abilities.

Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 25,000 employees and operations in the US, UK, China, and Singapore.

Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.

You will thrive in our inclusive and collaborative…