At a Glance
- Tasks: Ensure quality control of medical writing deliverables and provide leadership to the team.
- Company: Join a leading clinical research organisation with a focus on innovation.
- Benefits: Competitive salary, professional development, and a supportive work environment.
- Other info: Dynamic role with opportunities for career advancement and mentorship.
- Why this job: Make a real impact in clinical research while developing your leadership skills.
- Qualifications: 8+ years in clinical trial documentation and strong attention to detail required.
The predicted salary is between 46000 - 52000 £ per year.
Performs quality control review of Medical Writing deliverables from internal and external authors to ensure accuracy, consistency, and compliance with format and style requirements. Provides leadership, training, and guidance to staff, and assists in resource management.
Essential Functions
- Is a subject matter expert within the group and a source of advice and information to IQVIA staff on quality control processes;
- Conduct quality control (QC) review of a wide range of Medical Writing deliverables for both internal and external customers, including complex and substantial documents, with limited guidance and consistent high quality and efficiency;
- Document findings clearly, in accordance with defined procedures and checklists;
- Liaise promptly with document authors in case of questions or missing sources;
- Provide service metrics and scores, as required;
- Develop quality tools such as checklists, quality guidelines, standards and scoring methodology to meet project specific needs;
- May have responsibility for resourcing of QC tasks within the team;
- Take a leading role in providing training, guidance, and mentoring within the QC group;
- May take a formal supervisory role in managing QC staff and/or contract resources;
- Take a leading role in proposing, developing, evaluating, and implementing process changes and tools and monitoring their adoption and benefits;
- Take a leading role in QC team meetings and ensuring that lessons learned are shared and consistent approaches are applied;
- Contribute to budget proposals for QC tasks and maintain a clear understanding of the time and resources needed for tasks within remit;
- May take a leadership role for a stand-alone QC project, lead the team, and be the primary contact with the customer;
- May participate in project team meetings and liaise directly with the customer on QC issues, as appropriate and with senior support as needed;
- Take responsibility for on-time delivery of QC review comments;
- Manage daily assignments, planning and directing work, and take responsibility for managing workload for assigned projects and tasks, in collaboration with senior staff;
- Keep abreast of current data, trends, medical writing (MW)/regulatory knowledge, developments and advances in area of drug development/MW.
Qualifications
- Bachelor's Degree Life sciences related discipline or related field Req
- Master's Degree Life sciences related discipline or related field Pref
- Ph.D. Life sciences related discipline or related field Pref
- Typically, at least 8 years experience working with clinical trial documentation in a research environment, including significant experience of performing quality control (QC) review of clinical trial-related documents, defining and refining processes, and training and developing others.
Experience
- Requires in-depth understanding of the structure, format, and purpose of a wide range of MW deliverables and the importance of consistency, clarity, and accuracy versus sources. Req
- Careful attention to detail, accuracy, and consistency;
- Impeccable English language skills and ability to detect and correct grammatical, spelling, and language errors;
- Ability to understand scientific/medical documents and identify deficiencies, errors and inconsistencies;
- Familiarity with the structural and content requirements of clinical study reports, protocols, and similar documents;
- Proactivity and advanced organizational and time management skills and ability to prioritize workload effectively with commitment to deadlines;
- Ability to communicate clearly, concisely, and effectively in English, both in writing and verbally, and confidence in using a range of communication methods to achieve results;
- Good understanding of clinical drug development and the functions, steps, and processes involved;
- Advanced understanding of the nature and purpose of Medical Writing deliverables;
- Ability to provide clear and effective guidance and training in the form of written instructions, presentations, and one-to-one discussion;
- Ability to provide thorough, appropriate, and sensitive feedback to less experienced colleagues;
- Confident use of Microsoft Office and Adobe Acrobat;
- Ability to quickly establish and maintain effective working relationships with co-workers, managers, and customers at a range of seniority levels.
Senior Clinical Editor London employer: Meeveem Limited
IQVIA is an exceptional employer for the Senior Clinical Editor role in London, offering a dynamic work culture that prioritises collaboration and professional growth. Employees benefit from comprehensive training opportunities, a commitment to quality, and the chance to lead innovative projects within a supportive team environment, all while being part of a leading organisation in the healthcare sector.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Clinical Editor London
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We think you need these skills to ace Senior Clinical Editor London
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for the Senior Clinical Editor London at Meeveem Limited, focus on highlighting your clinical experience and any specific training you've undergone. Include any relevant placements or internships you’ve completed, as well as any certifications that bolster your qualifications in human medicine.
Highlight Your Soft Skills:In the field of human medicine, soft skills are just as crucial as technical knowledge. Mention your communication skills, empathy, and teamwork experiences in your CV and cover letter. This shows that you can work well in a clinical setting and with patients, which is super important in this industry!
Tailor Your Cover Letter Thoughtfully:Be sure to personalise your cover letter for the Senior Clinical Editor London at Meeveem Limited. Mention why you’re passionate about human medicine and how you align with the company’s mission. This is your chance to convey your enthusiasm and make a case for why you'll be a valuable addition to the team!
Include Continuing Education:Make sure to mention any ongoing education or courses you’re taking to keep your skills sharp. In human medicine, staying updated with the latest practices is key. It shows you’re dedicated to your field, which employers like Meeveem Limited will definitely appreciate!
How to prepare for a job interview at Meeveem Limited
✨Brush Up on Clinical Knowledge
Since you're aiming for a role in human medicine, make sure you’re sharp on the latest clinical guidelines and practices relevant to the position. Be prepared to discuss case studies or scenarios you might encounter in the role. This will show that you're not just knowledgeable but also ready to apply that knowledge in real-life situations.
✨Demonstrate Soft Skills
In human medicine, technical skills are crucial, but don’t forget to showcase your soft skills like communication, empathy, and teamwork. In your answers, share specific examples of how you've worked effectively with patients or colleagues in the past, as these traits are highly valued in clinical settings.
✨Know Your CV Backwards
As you’re applying for a full-time position, your CV should tell a story. Be ready to discuss every part of it, especially your clinical experiences, the impact you had, and what you learned. Employers want to see how your journey has prepared you for this role, so think of it like you're taking them through your professional narrative.
✨Prepare for Ethical Scenarios
Ethics are a big deal in human medicine, so expect questions that assess your decision-making in tricky situations. Think about how you'd handle ethical dilemmas or patient confidentiality concerns. Prepare a few examples that illustrate your thought process and how you prioritise patient welfare in your decision-making.
