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Senior Regulatory Writing Specialist
Clinical & Nonclinical | Pharmaceutical Industry
About the Role
We are seeking a Regulatory Writing Specialist with at least 3 years of hands-on pharmaceutical regulatory writing experience, particularly in clinical development and regulatory submissions. The successful candidate will have direct authorship experience across multiple regulatory document types, strong document Quality Control (QC) skills, and the ability to manage client-facing projects and deliverables. Experience in nonclinical or preclinical writing, CMC documentation, and regulatory submission preparation would be an advantage.
Key Responsibilities
Clinical Regulatory Writing: Author and develop Clinical Study Reports (CSRs), clinical study protocols, Investigator's Brochures (IBs), briefing documents, briefing books, and other clinical regulatory documents.
Regulatory Submissions: Prepare and support documentation for IND, NDA, BLA, and MAA submissions, including CTD Module 2 documents such as the Clinical Overview (Module 2.5) and Clinical Summary (Module 2.7).
Nonclinical & Preclinical Writing: Where applicable, develop nonclinical summaries, overviews, and supporting documentation, including CTD Module 2.4, Module 2.6, and Module 4 documents.
Scientific Documentation: Work with clinical evidence reports, scientific source materials, statistical outputs, and, where required, Chemistry, Manufacturing and Controls (CMC) documentation.
Document Quality Control: Conduct QC reviews to verify scientific accuracy, consistency, references, data, tables, figures, formatting, and compliance with project-specific requirements.
Project Management: Liaise with clients and cross-functional teams, manage review comments and document revisions, and coordinate deliverables to meet agreed timelines.
Must-Have Requirements
At least 3 years of hands-on pharmaceutical regulatory writing experience, with substantive document authorship rather than contribution or review alone.
Clinical regulatory writing experience.
Direct authorship of at least 3 different types of regulatory documents, such as CSRs, clinical protocols, Investigator's Brochures, briefing documents, or CTD Module 2 documents. Client-facing and/or project management experience.
Practical document QC review experience and excellent attention to detail.
Advanced Microsoft Word skills, including complex formatting, styles, tracked changes, tables, and document review.
Excellent written English, scientific communication, and organisational skills.
Optional Requirements
PhD, PharmD, MD, or another relevant scientific or medical qualification.
Nonclinical or preclinical regulatory writing experience, particularly CTD Module 2.4, Module 2.6, or Module 4.
Scientific, pharmaceutical, clinical, or research experience.
Familiarity with CMC documentation and regulatory submission requirements.
Experience with Veeva Vault, SharePoint, PleaseReview, or similar document management platforms. Basic understanding of biostatistics and clinical study data interpretation.
Familiarity with ICH guidelines and FDA or EMA regulatory requirements.
Ideal Candidate
A detail-oriented regulatory writer who can independently author high-quality clinical regulatory documents, interpret scientific information, perform rigorous QC, and manage client deliverables in a pharmaceutical environment.
Important:
This role requires demonstrable writing experience, not solely document coordination, proofreading, or QC review.
Please submit your CV highlighting the regulatory documents you have personally authored, your clinical regulatory writing experience, and your QC and client-facing responsibilities.
WORK ENVIRONMENT
Remote - Europe
Disclaimer
The company has reviewed this job description to ensure that essential functions and basic duties have been included. It is intended to provide guidelines for job expectations and the employee's ability to perform the position described. It is not intended to be construed as an exhaustive list of all functions, responsibilities, skills, and abilities. Additional functions and requirements may be assigned by supervisors as deemed appropriate. This document does not represent a contract of employment, and the company reserves the right to change this job description and/or assign tasks for the employee to perform, as the company may deem appropriate.
By attaching your Curriculum Vitae (CV), resume, and/or completing an online application, you are consenting to the collection, processing, use, transfer (including but not limited to other countries/jurisdictions), storage, and disclosure of your personal data as described in the Med Communications, Inc. Privacy Policy. Please read this policy carefully for more information on your rights regarding personal data protection.
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, disability, genetic information, or veteran status.
Recruitment Agency Notice:
Thank you for your interest in working with Med Communications. We kindly ask that recruitment agencies avoid sending unsolicited CVs, as our in-house team manages all hiring processes.
Please be aware that any unsolicited CVs or candidate profiles received without prior engagement or agreement with our recruitment team will be considered free and carry no obligation on the part of Med Communications. We thank you for your compliance with our policy.
Should collaboration opportunities arise, we will reach out to preferred partners proactively. Your understanding and cooperation are appreciated.
