Senior Regulatory Affairs Associate - Generalist

Parexel; Charleston (WV); On-site; USD 90,000 - 140,000; Full time

Job summary

Parexel is seeking a Regulatory Affairs Generalist / Senior Associate to support a strategic pharmaceutical partnership, handling end-to-end regulatory activities across clinical, submission, and post-approval work. The role collaborates with internal teams and alliance stakeholders to ensure regulatory excellence.

You will manage archiving, submissions, and cross-functional regulatory planning, attend alliance meetings, and contribute to lifecycle regulatory maintenance for assigned programs.

Qualifications

• 3+ years of regulatory affairs experience in an industry-related environment.
• Bachelor’s Degree in a Scientific or Technical Discipline required; Advanced Degree preferred.

Responsibilities

• Regulatory Archiving & Documentation Management: Maintain U.S. regulatory archive logs, record new submissions, archive authority correspondence, manage partner correspondence, ensure proper indexing and audit readiness.
• Clinical Regulatory Support: Maintain trackers for Form FDA 1572, perform GLP reviews, author 1572 waivers, support routine clinical submissions, attend cross-functional trial team meetings as Regulatory Affairs representative.
• Regulatory Submission Preparation: Draft administrative submission components, build electronic submission structures, manage workflows, coordinate delivery with publishing teams.
• Global Regulatory Team & Cross-Functional Collaboration: Prepare GRT materials, represent Regulatory Affairs in alliance meetings, support cross-functional program meetings.

Skills

Project management

Client-focused

Results orientation

Teamwork

Consulting

Interpersonal communication

Critical thinking

English proficiency

Education

Bachelor’s degree in a Scientific or Technical Discipline

Job description

We are seeking a highly organized and collaborative Regulatory Affairs Generalist / Senior Associate to support a strategic pharmaceutical partnership and its associated development and commercial programs. This role is dedicated to providing end‑to‑end regulatory affairs support for partnered assets, working closely with internal teams and external alliance stakeholders to ensure regulatory excellence across clinical, submission, and post‑approval activities.

Serving as a key regulatory interface within the partnership, the Regulatory Affairs Generalist / Senior Associate plays a critical role in regulatory planning, documentation management, submission execution, and ongoing compliance with global regulatory requirements. The ideal candidate thrives in a dynamic, cross‑company environment, effectively balances multiple priorities, and brings strong communication, problem‑solving, and collaboration skills to support successful partnership outcomes.

The Regulatory Affairs Generalist / Senior Associate provides comprehensive support across clinical, submission, and post approval regulatory activities for assigned pharmaceutical products and development programs. This role works cross functionally to ensure operational excellence in regulatory planning, documentation management, submission execution, and compliance with global regulatory requirements. The ideal candidate thrives in a dynamic environment, is highly organized, and demonstrates strong communication and problem-solving skills.

Key Responsibilities

1. Regulatory Archiving & Documentation Management

• Maintain U.S. regulatory archive logs, including:

• Recording new submissions.

• Archiving regulatory authority correspondence.

• Upload and manage correspondence from global partners for assigned programs.

• Ensure proper indexing, version control, and compliance using Regulatory Information Management (RIM) systems, electronic document management systems (EDMS), or other applicable archiving tools.

• Ensure records are complete, audit ready, and aligned with internal SOPs and regulatory expectations.

1. Clinical Regulatory Support

• Maintain and update trackers for Form FDA 1572 waiver requests and other clinical regulatory documentation.

• Conduct GLP reviews of study documentation on behalf of Regulatory Affairs to support IND level compliance.

• Author 1572 waiver requests and support routine regulatory submissions for clinical investigators.

• Attend cross functional clinical trial team meetings as the Regulatory Affairs representative, providing regulatory interpretation, updates, and risk assessments.

1. Regulatory Submission Preparation

• Draft administrative components of regulatory submissions, including:

• FDA forms

• Cover letters

• Submission metadata and other supporting documents

• Build and organize electronic submission structures using RIM systems or industry standard submission planning tools.

• Manage internal workflows and approval processes to ensure timely completion of submission components.

• Coordinate submission package delivery through established publishing workflows and oversee communication with submission/publishing teams.

1. Global Regulatory Team (GRT) & Cross Functional Collaboration

• Prepare presentation materials and slide decks for Global Regulatory Team (GRT) meetings, governance discussions, and alliance meetings.

• Serve as the Regulatory Affairs representative in partner or alliance meetings for assigned products, providing updates and tracking action items.

• Support ongoing cross functional program meetings as needed, ensuring regulatory deliverables and timelines remain on track.

1. Authoring & Reviewing Regulatory Submissions

• Contribute to the drafting, review, and preparation of regulatory submissions across development phases, including:

• FDA meeting requests

• Briefing documents

• Applications for special regulatory designations (e.g., Fast Track, Orphan Drug Designation)

• IND submissions, amendments, and associated documentation

• Ensure content is scientifically sound, consistent, clear, and aligned with regulatory standards and internal templates.

1. Post Approval Regulatory Maintenance

• Prepare, review, and submit periodic post marketing regulatory reports for assigned products, including:

• PADERs (Periodic Adverse Drug Experience Reports)

• NDA Annual Reports

• DSURs (Development Safety Update Reports)

• PBRERs (Periodic Benefit Risk Evaluation Reports)

• Maintain tracking and compliance with global post approval commitments, submission deadlines, and regulatory requirements.

• Support lifecycle management activities to ensure continued product compliance.

Skills

• Project management knowledge

• Client-focused approach to work

• Results orientation

• Teamwork and collaboration skills

• Consulting skills

• Excellent interpersonal and intercultural communication skills, both written and verbal

• Critical thinking and problem-solving skills

• Proficiency in local language and extensive working knowledge of the English language

Knowledge and Experience

• 3+ years of related regulatory affairs experience in an industry-related environment.

Education

• Minimum of a Bachelor’s Degree in a Scientific or Technical Discipline, Advanced Degree Preferred.

Other

• Due to the client’s location, candidates located in the Eastern or Central time zones of the US or Canada are preferred.

#LI-LB1

#LI-REMOTE

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.