Senior Medical Writer at Precision AQ

, , United Kingdom -

Full Time

Start Date

Immediate

Expiry Date

19 Jan, 26

Salary

0.0

Posted On

21 Oct, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Medical Writing, Content Development, Literature Searches, Communication Skills, Interpersonal Skills, Project Management, Team Collaboration, Regulatory Review, Client Interaction, Problem Solving, Attention to Detail, Microsoft Word, PowerPoint, Excel, Adobe Acrobat, PubMed

Industry

Business Consulting and Services

Description

Job summary and scope: The primary responsibility of the Senior Medical Writer I (SMW I) is to ensure that all content developed is evidence-based, is of the highest editorial quality, meets the strategic objectives of our clients, and ultimately translates science into clinical benefit. The SMW I is expected to be able to effectively collaborate with all team members to drive project to efficient completion. The SMW I should be engaged in frequent collaboration with the Principal Medical Writer (PMW)/Scientific Director, (ScD) while also developing independence as a content lead. Importantly, the SMW I should have the expertise and confidence to lead content discussions with a client, guide projects through Medical-Legal-Regulatory review processes, identify problem areas and propose solutions, and understand and apply the strategic imperatives of the client to all content development. Key responsibilities: Content Development Display excellent written and verbal communication skills. Write to the standards, format, and requirements of our clients. Engage in detail-oriented approaches, supporting the creation of complete, thorough, and accurate content. o Complete all elements required by team and client, such as speaker notes, references, annotations, etc. o Organise and annotate references in accordance with internal standards and client requirements. Independently conduct effective literature searches and identify project-related key data and/or information. o Interpret and apply clinical and preclinical data from complex tables and graphs with ease. o Learn new subject areas quickly according to business needs. Develop multiple drafts of content in various forms up to and including the final draft that is submitted for dissemination and/or publication. o Including, but not limited to outlines, slide decks, speaker notes, manuscripts, monographs, executive summaries, and meeting materials. Implement internal and external comments and feedback thoroughly and effectively; other internal team members such as the overseeing SD should be able to review with confidence. Understand and apply the strategic imperatives of the client to content development. o Includes the development of outlines with a clearly highlighted story arc. Internal and External Collaboration Display excellent interpersonal and teamwork skills. Interface with internal team members as required in order to support a mutual understanding of project objectives, timing expectations, and next steps. o Provide clear direction and collaborate effectively with the Editorial and Creative staff. Confidently balance multiple tasks and multiple priorities. Understand and plan around budgeted project hours, efficiently complete work within the allotted time or flag challenges and suggested solutions. Work closely and effectively with internal reviewers (eg, PMW/ScD/Accounts) to meet the standards and expectations of our company and our clients. Manage projects effectively and collaborate with internal teams on next steps, not requiring substantial PMW/ScD oversight. Work with minimal supervision, including consistently managing own workload and priorities. Proactively identify issues and potential pitfalls. Interact with clients and external experts in various formats, such as live meetings, teleconferences, and webinars. Lead content-related discussions with clients and external experts, sometimes in conjunction with the PMW/ScD, but also be able to manage these conversations independently. Lead the internal team in the medical/legal/regulatory review process, including answering queries, understanding the changes required, and guiding the internal team on implementing these changes. Required Processes and Tools Proficiency in using Microsoft Word®, PowerPoint®, Excel®, Adobe Acrobat®, and reference-management software (e.g., EndNote®), as required by specific team need. Proficiency with PubMed and other literature search tools. Ability to quickly learn and apply relevant style guides. Consistent and effective use of communication tools such as Teams for internal trafficking and collaboration. Timely completion of training assignments, annual leave planning, and individual evaluations in the relevant systems. Familiarity with current ABPI code of practice #LI-TB1 #LI-Remote Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice. Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com. It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.

Responsibilities

The Senior Medical Writer I is responsible for developing high-quality, evidence-based content that meets client objectives. This role involves collaboration with team members and clients, leading content discussions, and managing projects through various review processes.