對於沒有什麼投稿經驗的研究者來說,在投稿上常常碰到許多難題,不是抓不到方向,就是寫作技巧不夠熟練
而在投稿國際期刊上面的成功機率就不高,時常碰壁....
面對這樣的困境,要推薦給各位一個很棒的資源!!
BMJ和加州大學舊金山分校(UCSF)攜手合作,針對醫學領域提供了一個投稿及研究方法的線上課程
內容從理論到寫作方法,除了教導我們怎麼投稿,也提供了如何設計研究試驗的技巧!對於研究者來說可是一大福音
結合國際出版社與專業學者共同打造的線上專業'課程,藉此希望可以提供投稿品質以及投稿的成功率,趕緊體驗看看吧!
Rsearch to Publication是BMJ與加州大學舊金山分校(UCSF)和做為醫學領域的研究員新手量身打造的線上學習課程。
不同於一般的科技論文寫作訓練,該課程完全是針對醫學研究,
由《英國醫學雜誌》資深研究編輯和UCSF學者現身說法,
按步指引學員瞭解、洞悉醫學研究的整個過程:從如何設計一個研究到投稿並成功發表在國際醫學期刊。
提供效益:
- 由BMJ編輯群以及UCSF專業知識建立
- 改善研究產出的品質
- 提升稿件出版的機率
- 獨有專注於醫學研究
- 具有彈性、獨立的線上學習課程
- 課程結業證書授予
- 提供免費試用,若訂購模組回饋投稿BMJ Open
可享稿件審閱費用75%off
總共提供6大課程、48個模組。模組可獨立學習使用,內容互相連貫,學員可以依本身程度和進度,
自由選擇合適的模組,並由自己掌握適合的速度作學習。
BMJ課程
|
How to Write a Paper ? 如何撰寫論文?
|
- The introduction: presenting the research question
- The methods: matching study designs to research questions
- Ethics aspects of study methods
- Reporting statistical methods and analyses
- The results: reporting all findings succinctly
- The discussion: using structure and balance
- Choosing and citing references
- Optimising the abstract and title
|
What Editors and Peer Reviewers Look For ?
期刊編輯和同行評審尋求的是什麼?(6)
|
- Compliance with Journal and ICMJE requirements
- Navigating Journal and Peer Review Processes
- Surviving Peer Review
- What to do with rejections and appeals
- Pre-submission inquiries and cover letters
- Good medical writing
|
Publication Ethics 瞭解出版倫理 (8)
|
- Patients' consent for publication
- Journal rules on authorship
- Reporting conflicts of interest
- How to write up industry-sponsored trials
- Scientific transparency: the pitfalls of selective reporting
- How and why to avoid plagiarism
- How journals uncover scientific fraud
- How journals act on scientific misconduct
|
UCSF課程
|
Designing Clinical Research 如何設計臨床研究?(9)
|
- The Research Question
- Study Design including Observational Studies, Randomized Blinded Trials, and Studies of Medical Tests
- Subjects and Variables
- Enhancing Causal Inference
- Sample Size and Power
- Statistics
- Data and Safety Monitoring
- Questionnaires and Qualitative Research
- Ethical Considerations in Research
|
Responsible Conduct of Research 確保研究方案盡責執行 (11)
|
- Trial Designs
- Randomization
- Selection of Participants
- Blinding
- Choosing the Intervention and Controls
- Recruitment
- Adherence and Complete Follow-up
- Outcome Measures
- Adverse Events
- Regulatory Issues
- Ethical Issues in Clinical Trials
|
Introduction to Clinical Trials瞭解臨床試驗 (6)
|
- Overview of Clinical Research Regulations, including: a) History of Research Regulations; b) Assessing Risks and Benefits; and c)
- Practical Issues in IRB Reviews
- Informed Consent and Related Issues, including: a) Informed Consent; and b) When Consent and IRB Review are Not Needed Conflicts of Interest
- Authorship
- Research Misconduct
- Research in Resource-Poor Environments
|
提供兩個模組免費體驗,快上網進行登錄!
www.rtop.bmj.com
留言列表