![]() ![]() Broad experience in preparation of all types of clinical regulatory documentation.Demonstrated understanding of clinical research, the drug development process, and applicable regulatory guidelines and regulations.Provides departmental expertise and perspectives to promote prospective business opportunities provide Parexel colleagues with pertinent information to formalize a sound business strategy.Ability to gain trust and confidence within the company. Establishes a connection with the client beyond one's project, to gain repeat business and/or to widen existing scope and services.Understands and satisfies client needs.Ability to negotiate on behalf of medical writing to ensure resources, timelines and expectations are aligned.Presents solutions and follows through to ensure problems have been satisfactorily resolved. Exhibits sound judgement: escalates issues to project teams or departmental management as appropriate.Possesses team leadership skills and cross-cultural sensitivity. Competent working in a matrix environment and values the importance of teamwork.Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail, e.g., organizational skills.Motivation to work consistently in a fast-paced, rapidly changing environment.A flexible attitude with respect to work assignments and new learning.Excellent interpersonal, negotiation, verbal, and written communication skills. ![]() ![]() The Principal Medical Writer also facilitates process improvement and technical mentoring/training and supports Medical Writing Services management during the sales process by providing client liaison and proposals input. The Principal Medical Writer may operate as the project lead writer/submission coordinator and primary client contact to manage contributions of multiple writers working on related documents. The Principal Medical Writer will research, create, and edit all documents associated with clinical research. This role can be fully home based in various European countries such as Belgium, Croatia, Czech Republic, Denmark, France, Finland, Germany, Hungary, Ireland, Italy, Lithuania, Poland, Romania, Serbia, Spain, Sweden or the UK. We are looking for a Principal or Senior Medical Writer due to an ever expanding team. From clinical trials to regulatory, consulting, and market access, our therapeutic, technical, and functional ability is underpinned by a deep conviction in what we do. We believe in our values Patients First, Quality, Respect, Empowerment & Accountability. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. Parexel is in the business of improving the world’s health. ![]()
0 Comments
Leave a Reply. |
AuthorWrite something about yourself. No need to be fancy, just an overview. ArchivesCategories |