Associate Regulatory Writer Graduate
Associate Regulatory Writer Graduate

Associate Regulatory Writer Graduate

Full-Time 25000 - 37000 ÂŁ / year (est.) Home office (partial)
Go Premium
LinkedIn

Job Title: Associate Regulatory Writer Graduate Location: White City, LondonContract: 12 Months / Hybrid 3 days onsite Hours: 37.5 per week Rates: £31,050 p/a Job DescriptionSRG 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 RWS.Main sub-team representative at the Clinical Trial Team (CTT).Participate in planning of data analyses and presentation used in CSRs.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 RWS.Maintain audit, SOP and training compliance.Experience and QualificationsEducation:(minimum/desirable)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 perspectiveUnderstanding of matrix environmentGlobal, cross-cultural perspective and customer orientation.

Associate Regulatory Writer Graduate employer: LinkedIn

Join a leading pharmaceutical company in White City, London, where you will be part of a dynamic team dedicated to producing high-quality clinical documentation. With a strong emphasis on employee growth and development, the company offers a supportive work culture that encourages collaboration and innovation. Enjoy the benefits of a hybrid working model, competitive salary, and the opportunity to contribute to impactful projects in the healthcare sector.
LinkedIn

Contact Detail:

LinkedIn Recruiting Team

Associate Regulatory Writer Graduate
LinkedIn
Go Premium

Land your dream job quicker with Premium

You’re marked as a top applicant with our partner companies
Individual CV and cover letter feedback including tailoring to specific job roles
Be among the first applications for new jobs with our AI application
1:1 support and career advice from our career coaches
Go Premium

Money-back if you don't land a job in 6-months

>