[IQVIA™ (formerly QuintilesIMS)] Medical Writer
[IQVIA™ (formerly QuintilesIMS)] Medical Writer
IQVIA™ (formerly QuintilesIMS) 외국계기업
서울시 송파구 송파대로 558 월드타워 13층 / 서울시 중구 충무로 3가 60-1 남산스퀘어 빌딩 23층
IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.
Join Us
Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.
Forge a career with greater purpose, make an impact, and never stop learning.
IQVIA 는 데이터 및 과학을 활용한 지식 정보, 혁신적인 기술 솔루션 및 CRO 분야의 세계적인 선도기업으로 보건의료 고객들이 환자들을 위한 보다 나은 솔루션을 제공할 수 있도록 지원하고 있습니다. IMS health 와 Quintiles 의 합병을 통해 설립된 아이큐비아(IQVIA)는 전세계 약 60,000여명의 전문가들이 근무하며 human data science 의 잠재력을 실현하기 위해 노력하고 있습니다.
Job Description
PURPOSE
Prepares, or contributes to the preparation of more advanced or complex clinical documents, method validation and study data reports, site manuals, or posters, for either internal Quintiles customers or external clients, for investigational drugs, biologicals, or medical devices, under the guidance of senior staff. Participates in project teams and may lead specific tasks, consulting senior staff as necessary.
RESPONSIBILITIES
Acts as Lead Medical Writer on more advanced writing projects and performs competently, with guidance from senior staff as required. Takes responsibility for preparation of assigned documents to a high standard, working in accordance with Quintiles SOPs and the customer’s requirements. Identifies project needs, tracks project timelines and implements client requests with senior review.
Participates in both internal and external project team meetings and liaises directly with the customer on medical/technical writing issues, including setting of project timelines, as appropriate and with senior support as needed.
Facilitates appropriate internal review of assigned documents and takes responsibility for on-time delivery.
May perform QC review of documents or parts of documents prepared by more senior staff.
May deliver basic level training to small groups or individuals within Quintiles on the role of the medical/technical writing processes and specific client report templates, processes, and requests.
Takes responsibility for managing workload for assigned projects and tasks, in collaboration with senior staff.
Keeps abreast of current data, trends, medical and/or technical writing/regulatory knowledge, developments and advances in area of drug development/medical and/or technical writing.
Complies with Company SOPs and participates in the implementation of new SOPs.
Job Requirements
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
Excellent standard of written English, and ability to communicate fluently and effectively in English, both in writing and verbally.
Familiarity with the structural and content requirements of clinical or method validation and study reports, protocols, and similar documents for internal and external clients.
Ability to integrate, interpret, and summarize data from a variety of sources in a clear and concise manner.
Competence in completing good first draft technical reports or clinical reports within a standard timeframe with limited guidance.
Good understanding of common statistical methods used in clinical trials or pharmaceutical work and/or interpretation of their results.
Ability to give a presentation to a project team and/or customer on project-specific topics, e.g. on lessons learned.
Ability to identify deficiencies, errors, and inconsistencies in a protocol or report.
Ability to effectively review a statistical analysis plan and to identify deficiencies, errors, and inconsistencies in statistical output as related to acceptance criteria according to SOPs.
Confidence in building relationship with customer and discussing medical/technical report writing issues with customers in person, via e-mail or on the telephone.
Can provide thorough, appropriate and sensitive feedback to peers upon request to review a document.
Ability to work on several projects at once while balancing multiple and overlapping timelines.
JOB DESCRIPTION
Ability to assess workload and suggest prioritization to senior staff.
Demonstrated abilities in collaboration with others and independent thought.
Knowledge of regulations relevant to medical writing/technical writing, such as Good Laboratory Practices (GLP) and other relevant regulatory agencies (e.g., OECD, MHLW).
Careful attention to detail and accuracy.
Must be computer literate.
Ability to establish and maintain effective working relationships with coworkers, managers and clients.
MINIMUM REQUIRED EDUCATION AND EXPERIENCE
Bachelor’s degree in a life science-related discipline, communications, technical writing, or related field, with at least 5 years of experience in a medical, clinical, preclinical, chemistry or related environment; or equivalent combination of education, training and experience.
PHYSICAL REQUIREMENTS
Extensive use of telephone and face-to-face communication requiring accurate perception of speech
Extensive use of keyboard requiring repetitive motion of fingers
Regular sitting for extended periods of time
May require occasional travel.
Additional Information
커리어수준: 대리과장.5년이상
급여사항 : 면접 후 협의
고용형태 : 정규직
경력여부 : 경력
Guidelines for Applicants
전형방법 : 1차 서류전형-2차 면접전형
제출서류 : 한글이력서, 영문이력서, 한글자기소개서 (각종 증빙서류는 서류전형합격자에 한해 추후제출)
접수방법 : 홈페이지
https://iqvia.wd1.myworkdayjobs.com/IQVIA/job/Seoul-Republic-of-Korea/Medical-Writer_R1163636
마감일 : 2021.11.19
채용담당 : 인사담당자 / +82-2-2046-8896 / koreaTA@iqvia.com
The Others
- 면접은 서류전형 합격자에 개별통지 합니다.
- 국가보훈대상자와 신체장애자는 관련서류 제출시 관계법에 따라 우대함.
- 모든 서류는 반드시 MS Word로 작성하기 바랍니다.
- 제출하신 서류는 일체 반환하지 않습니다.
- 입사지원서 내용에 허위사실이 판명될 경우 입사가 취소될 수 있습니다.
- 기타 문의사항은 E-mail로 문의바랍니다.