Job Title: Associate Regulatory Writer Graduate Location: White City, London Contract: 12 Months / Hybrid 3 days onsite Hours: 37.5 per week Rates: £31,050 p/a 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/desirable) Minimum university life science degree or equivalent is required. Advanced degree or equivalent education/degree in life sciences/healthcare is desir...