Principal Regulatory Writer (Temporary)

Vir Biotechnology; Deutschland; Vor Ort; EUR 217.210 - 241.344; Vollzeit

Zusammenfassung

Vir Biotechnology is hiring a Principal Regulatory Writer (Temporary) in Germany to support regulatory submissions writing. This role involves crafting clear, compliant documents and collaborating with cross-functional teams.

Applicants should have 15 to 20 years of experience, particularly with regulatory documents like Clinical Study Reports and protocols. The role offers a competitive hourly pay range of $180 to $200, commensurate with experience and qualifications.

Qualifikationen

• 15 to 20 years of relevant experience required.
• Experience with regulatory documents like CSRs, IBs, and protocols.
• Expert understanding of ICH guidelines and GxPs.

Aufgaben

• Craft compliant documents for regulatory submissions.
• Write and edit a wide range of regulatory documents.
• Manage medical writing projects and timelines.

Kenntnisse

Regulatory document writing

Cross-functional collaboration

Project management

Complex scientific analysis

Ausbildung

Bachelor's degree

Advanced degree in science or medical field

Tools

eCTD structure

Jobbeschreibung

Vir Biotechnology, Inc. is a clinical‑stage biopharmaceutical company focused on powering the immune system to transform lives by discovering and developing medicines for serious infectious diseases and cancer. Its clinical‑stage portfolio includes programs for chronic hepatitis delta and multiple PRO‑XTEN® dual‑masked T‑cell engagers across validated targets in solid tumor indications. Vir Biotechnology also has a preclinical portfolio of programs across a range of infectious diseases and oncologic malignancies.

THE OPPORTUNITY

Vir Biotechnology is looking for a Principal Regulatory Writer (Temporary) who will support all aspects of regulatory submissions writing needs. You will collaborate with senior management and other leads to support consistent documents/messaging within and across programs.

This Person will report to the Senior Director, Regulatory Writing.

WHAT YOU'LL DO

• Craft clear, accurate, and compliant documents required for regulatory submissions to global health authorities including FDA and EMA.
• Write and edit a wide range of regulatory documents, including but not limited to: Clinical trial protocols and amendments, Investigator Brochures (IBs), Clinical Study Reports (CSRs), briefing packages, internal/external facing labeling documents (eg, CCDS/CCSI, annotated draft labels, IFU, patient leaflets, etc), and components of regulatory submission dossiers (eg, NDA, IND, MAA) such as Module 2 and 5 summary documents (eg, SCS, SCE, ISS, etc).
• Ensure that all written materials strictly adhere to regulatory guidelines, industry standards, and internal quality standards.
• Analyze complex scientific and medical information, including clinical trial data, translating it into clear, concise, and accurate language understandable by both technical and non‑technical audiences.
• Work closely with cross‑functional teams (eg, clinical research and operations, biostatistics, regulatory affairs, pharmacology, safety, etc) to ensure comprehensive and accurate document content.
• Manage medical writing projects, including developing timelines and communicating with cross‑functional team members to maintain awareness of review cycles and expectations.
• Participate in cross‑functional meetings to provide input regarding medical writing deliverables, timelines, and any processes needed for the completion of regulatory documents.
• Participate in defining and writing standard operating procedures and best practices for efficient preparation of quality documents.
• Provide teams with guidance about best practices and industry standards, offer solutions to authoring hurdles, support interaction and understanding across functional areas.

WHO YOU ARE AND WHAT YOU BRING

• Bachelor's degree and 15 to 20 years of relevant experience required. Advanced degree in science or medical field is a plus.
• Experience with all common study‑level and submission‑level regulatory documents such as CSRs, IBs, DSURs, protocols, and eCTD modules required.
• Proven experience with marketing applications (INDs, BLAs, NDAs, MAAs, or equivalents) including responses to health authorities, 90/120‑day safety updates, or other post‑submission activities required.
• Expert understanding of eCTD structure and the clinical development process, and in‑depth knowledge of document‑related ICH guidelines and GxPs.
• Proven ability to manage complex projects and influence cross‑functional teams.

WHO WE ARE AND WHAT WE OFFER

The expected hourly range for this position is $180.00 to $200.00. Actual pay will be determined based on experience, qualifications, geographic location, and other job‑related factors. Applicants must currently be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

All employment decisions at Vir Biotechnology are based on legitimate, non‑discriminatory business requirements, job duties and individual qualifications. Employment decisions are made without regard to any legally protected characteristics. This commitment extends to all management practices and decisions, including recruitment and hiring, compensation, appraisal systems, promotions, training and career development programs. Vir Biotechnology also strongly commits to providing employees with a work environment free of unlawful conduct or harassment.

Vir Biotechnology Human Resources leads recruitment and employment for Vir Biotechnology. Unsolicited resumes sent to the company from recruiters do not constitute any type of relationship between the recruiter and Vir Biotechnology and do not obligate us to pay fees should we hire from those resumes. We ask that external recruiters and/or agencies not contact or present candidates directly to our hiring manager or employees.

For hires based in the United States, Vir Biotechnology participates in E‑Verify.