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Associate regulatory writer graduate

London
SRG
Regulatory writer
€100,000 - €125,000 a year
Posted: 3h ago
Offer description

Social network you want to login/join with: Associate Regulatory Writer Graduate, London

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SRG Location:

London, United Kingdom Job Category:

Other - EU work permit required:

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2047c691c821 Job Views:

4 Posted:

14.07.2025 Expiry Date:

28.08.2025 col-wide Job Description:

Job Title: Associate Regulatory Writer Graduate Location: White City, London Contract: 12 Months / Hybrid 3 days onsite Job Description SRG are looking for an associate regulatory writer to join a leading pharmaceutical company based in London. The main purpose of this role is to write and/or edit under guidance high quality clinical and safety documentation. Duties and Responsibilities To write and/or edit under guidance high quality clinical and safety documents: Clinical Study Protocols (CSP) and protocol amendments, non-registration Clinical Study Reports (CSR), Development Safety Update Reports (DSUR), Clinical Trial Registration Documents. May coordinate outsourced activities in Main sub-team representative at the Clinical Trial Team (CTT). Participate in planning of data analyses and presentation used in May act as documentation consultant in CTTs to ensure compliance of documentation to internal company standards and external regulatory guidelines. May act as liaison between CTTs and publishing teams to ensure timely delivery of final documents for publishing. May contribute to development of processes within Maintain audit, SOP and training Experience and Qualifications Education: Minimum university life science degree or equivalent is required. Advanced degree or equivalent education/degree in life sciences/healthcare is desirable. Languages: Fluent English (oral and written). Experience / Professional Requirement: · Some medical writing experience or other relevant pharma industry experience combined with scientific and regulatory knowledge. · Understanding of global regulatory environment and process (key regulatory bodies, key documents, approval processes, safety reporting requirements). · Excellent communication skills (written, verbal, presentations) · Understanding of biostatistics principles. · Ability to prioritize and manage multiple demands and projects. · Ability to define and solve complex problems ("Problem- solver") · Broad knowledge and future oriented perspective · Understanding of matrix environment · Global, cross-cultural perspective and customer orientation.

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