Job Description
Principal Medical Writer (Regulatory / Clinical)Principal Medical Writer (Regulatory / Clinical) - Global CRO – Home based in UK, Ireland or Spain - £negotiable + private healthcare, private dental, up to 10% company contribution pension, 25 days holidayA global CRO is currently recruiting a Principal Medical Writer (Regulatory / Clinical) to join them on a permanent basis. The role is 100% remote and you will need to be currently based in the UK, Ireland or Spain.The CompanyA global, well-known CRO is now recruiting for a Principal Medical Writer (Regulatory / Clinical) to join their already well-established team. Offering great training and development, this company has a huge interest in developing their employees to a high standard.Global CROWorking across multiple therapy areasVery exciting projects to work on and upcoming pipelineExcellent career progression opportunities to Senior Regulatory Writer and beyondGreat training and developmentThe RoleWorking on a number of exciting projects and with an exciting pipeline, the Principal Medical Writer (Regulatory / Clinical) will be responsible for:Writing, editing, and reviewing documents such as Clinical Study Reports, Protocols, Informed Consent, Safety Aggregate Reports (DSUR/PBRER), Safety Narratives, Clinical summaries / CTD sections to Clinical Overviews, etc.Managing multiple projects concurrentlyReviewing all documentation to a high standardWorking across multiple therapy areasMeeting both internal/external deliverables against set timelinesWorking closely with others in the writing team e.g., Senior Regulatory WriterYouTo apply for this role as Principal Medical Writer (Regulatory / Clinical), our client is hoping for someone with the following skills and experience:Ample experience in a Medical Writing / Regulatory Writing roleExperienced within a CRO or Pharma settingExperienced writing, editing, and reviewing documents such as Clinical Study Reports, Protocols, Informed Consent, Safety Aggregate Reports (DSUR/PBRER), Safety Narratives, Clinical summaries / CTD sections to Clinical OverviewsAbility to work in a fast-paced environment, meeting internal and external deliverablesAbility to manage multiple projects at onceAny therapy area experience will be considered within CRO or PharmaWhat should you do next?This Principal Medical Writer (Regulatory / Clinical) role is one not to be missed; it encompasses the opportunity to work in a global CRO, across multiple therapy areas and with a range of clients. To discuss further, please submit your current CV, or to chat through other Medical Writer opportunities I'm working on within Regulatory Affairs, give me a call today.Unless otherwise stated, if applying for a job within the UK or European Union, you must ensure that you are already authorised to work there.Carrot Recruitment acts as an Employment Business and an Employment Agency on behalf of our client in recruitment for this role.We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, colour, sex, age, national origin, religion, sexual orientation, gender identity and/or expression.If there are any arrangements or adjustments we can make to assist you at interview, then please let us know and we'll be more than happy to assist. #J-18808-Ljbffr