l**********n
发帖数: 60 | 1 Title:
Pediatric pharmacovigilance by medication antidote signals and comparative
evaluation of their sensitivity with routine techniques of ADR detection in
hospitalized children
Journal: BMC Pharmacology Toxicology
需要两个审稿人审稿，有pharmacovigilance, adverse drug reactions, medication
antidote signals 相关背景就可以了。
有兴趣请站内联系。 |
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e**p
发帖数: 4259 | 2 pharmacovigilance里也有SAS programmer啊
就看你做什么了 |
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j******w
发帖数: 97 | 3 PV is focused on adverse event reporting and analysis, generally requires
some type of clinical experience, such as nursing.
Regulatory affairs is broader.
Go to indeed.com and search for pharmacovigilance jobs,you will get some
idea what type of responsibilities PV assumes.
Regulatory affairs has several major sub-areas, clinical, CMC, global,
submission management, labeling, ad/prom. It is a little tricky to get a
good understanding of the responsibilities. So try to find a "generalist/
strate... 阅读全帖 |
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i***m
发帖数: 148 | 4 这是完全不同的职业道路了，看你性格吧。
programmer是纯技术工种，不用跟人打交道。
pharmacovigilance有的也叫safety manager的，做的东西比较像文科，写safety
management plan啊，followup SAE啊，不知道你要不要做AE CM MH coding，跟人打交
道多一些。前景不是很清楚。 |
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l******1
发帖数: 12 | 6 If you are interested, please send your resume with the targeted position to
[email protected]
/* */, thanks.
1. Data Entry Coordinator
Location:Berkeley Heights, NJ
Total hours: 528
• Conduct full data entry from source document as per the GDSRM
conventions -all cases globally including complex cases involving medical
records and literature cases
• Interpretation of medical source documents for data entry into
the safety database including extraction of appropriate labor... 阅读全帖 |
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s**********8
发帖数: 25265 | 7 European Medicines Agency
The European Medicines Agency (EMA) is a European agency for the evaluation
of medicinal products. From 1995 to 2004, the European Medicines Agency was
known as European Agency for the Evaluation of Medicinal Products.[1]
Roughly parallel to the U.S. Food and Drug Administration (FDA), but without
FDA-style centralization, the European Medicines Agency was set up in 1995
with funding from the European Union and the pharmaceutical industry, as
well as indirect subsidy fr... 阅读全帖 |
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T*******t
发帖数: 1069 | 8 Multiple positions available. Fast growing pharmaceutical company, more
stable than most other companies in the industry. Most of the positions
are located in Mid West. Some of them are in CA.
For details, please mention the position you are interested in when you
reply to the following email address:
j******[email protected]
Please submit your resume when replying. This will help increase the
chance of your resume being reviewed vs. you submitting the resume
directly to the company HR or to the job s... 阅读全帖 |
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S******J
发帖数: 30 | 9 Senior Biostatistician-Programmer - Pharmacovigilance
Clinical R&D, Celgene
Summit, NJ
Responsibilities will include, but are not limited to, the following: 1.
Provide statistical and programming support to global drug safety/
Pharmacovigilance 2. Provide statistical input into the design of safety
analysis plan including table shells – coordinate with study team
statistician and lead safety MD 3. Analyze and report results of clinical
trials, individual protocol, and aggregate analyses at indic |
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s**********8
发帖数: 25265 | 10 Postmarketing surveillanceFrom Wikipedia, the free encyclopediaJump to:
navigation, search
Postmarketing surveillance (PMS) is the practice of monitoring the safety of
a pharmaceutical drug or device after it has been released on the market
and is an important part of the science of pharmacovigilance. Since drugs
are approved on the basis of clinical trials which involve relatively small
numbers of people who have been selected for this purpose - meaning that
they normally do not have other medi... 阅读全帖 |
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c***s
发帖数: 70028 | 11 3月30日，《法治周末》报以四个版的篇幅质疑科普作家、学术“打假斗士”方舟子自己也涉嫌抄袭。4月1日，方舟子接受羊城晚报记者专访时说，都是陈年老账，他早已一一澄清过。他还称“要告该报诽谤”。
《法治周末》报道指方舟子涉嫌抄袭的三篇文章分别是《现代药物是怎么开发出来的》、《科学是什么》、《科学地解决道德问题》。对2006年发表的《现代药物是怎么开发出来的》，方舟子当年就解释称，颖河的《认识药物》与他的文章均来自于美国FDA的一份材料，“只不过他的表达比较忠实于原文，我则采用复述”。方舟子昨天告诉记者，他的文章中有许多细节是颖河的文章中所没有的，所以并非抄袭他的。
《法治周末》指，《科学是什么》全文约1600字，其中约有900字几乎原文引自罗伯特教授的《神创论是科学的理论吗》。对此质疑，方舟子称，《科学是什么》是他1995年在中文网上跟人吵架时写的帖子，其中引用的科学判断标准只泛泛地说是科学的共识，1999年收入《方舟在线》时则注明是根据Root-Bernstein的归纳。
《法治周末》质疑《科学地解决道德难题》的主要内容与美国《科学》杂志上Greene等人的论文部分内容一致。方舟子介绍，... 阅读全帖 |
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d********t
发帖数: 837 | 12 当然。所以才会有pharmacovigilence 这个东西。但是更多的AE是在上市前就发现的，
然后写在label 里面。如果说上市以后也会有rare adverse events 被发现，就不需要
上市前做大规模三期，然后做integrated safety analysis, 这个逻辑也太奇葩了。
[在 Vasilii (瓦西里同志) 的大作中提到：]
:扯淡，就是上市的药也有小概率事件和长期服用的严重副作用。 |
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T*******t
发帖数: 1069 | 13 various oncology positions open, great pay, benefit and job security,
contact me for details
Associate Biostatistics Director, Oncology
Associate Director, Clinical Studies
Associate Director, CPED Science, Oncology
Associate Director, Quality Assurance, R&D Programs, GCP
Associate Director, Regulatory Affairs
Clinical Research Specialist
Director, In Vivo Pharmacology
Director/Senior Director, Discovery
Global Development Project Leader, Oncology
Medical Director/Senior Medical Director, Oncolo... 阅读全帖 |
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l*********g
发帖数: 94 | 14 求教。国内医学本科+这边生物PHD/统计Master. 多谢。 |
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g******n
发帖数: 339 | 15 在CRO不知道，在药厂当然要去PV。SAS programmer地位低下，上升空间极小，属于最
没有visibility的一类工作。当然现在outsourcing 挺多，SAS程序员在CRO工作机会不
少。 |
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l*********g
发帖数: 94 | 16 多谢指点。明白了。有什么PV的training可以增加机会吗？好像PV都要几年经验，申了
好多才有一个IV。 |
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w********a
发帖数: 621 | 17 Please contact me if you are interested.
Application Support Engineer – Billerica, MA
• Provide technical support for group's deployed applications,
track statuses of incoming support issues, and ensure each is addressed in a
timely manner
• Diagnose and fix production application problems, coordinating
with Project Managers and Engineers where necessary
• Bachelor's degree or equivalent; 2+ years’ experience in an
application support role
• Experience debuggi... 阅读全帖 |
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M********a
发帖数: 10 | 18 2013默沙东校园招聘北京大学宣讲会
亲爱的同学们，
默沙东校园招聘北京大学宣讲会
11月29日18：30北京大学北阁信息发布厅
今年默沙东中国为应届毕业生提供了近15个北京研发中心的职位，近200个销售培训生
职位（全国）和3个工程师职位（杭州/上海工厂）。
在此次北京大学的宣讲会中，我们邀请了默沙东亚洲研发总部的管理层和业务经理，将
和同学们亲密接触，介绍在北京的亚洲研发总部的职业发展和未来的发展计划，有意在
研发邻域开启职业生涯的同学请千万不要错过。
此次默沙东中国校园招聘的官方网站是http://campus.51job.com/msd, 欢迎大家点击访问，关注网申职位详情！
远见，我们共同穿越！
加入我们，成为世界领先制药企业的一员，为人类健康事业造福。
默沙东中国人力资源部门
<关于默沙东>
今天的默沙东正致力于为全世界带来健康的福音。我们为全球140多个国家提供药物、
疫苗、生物制剂、健康消费品和动物保健产品，并与客户一起提供创新的健康解决方案
。同时，我们还致力于通过各种意义深远的项目向需要帮助的人们捐赠和提供产品，从
而扩展人们进入医疗卫生的途径。默沙东，健康是福。
... 阅读全帖 |
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o********n
发帖数: 1329 | 19 From: HR Communications
Sent: Friday, September 20, 2013 11:10 AM
To: +Billerica-All Users; +Hackensack-All Users; +Perceptive-East Windsor; +
Perceptive-Wayne; +Waltham-All Users
Subject: Featured Job Openings for Northeast [on behalf of Rose Barsumian]
Featured Job Openings for Northeast
Do you know the perfect candidate for a job at PAREXEL?
These Featured Jobs highlight open positions in your local area and there
may be others so please check the Employee Referral website for a full
listing ... 阅读全帖 |
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l*********g
发帖数: 94 | 21 就是drug safety 和 medical coding啊，怎么会有programmer呢？ |
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l*********g
发帖数: 94 | 23 我是国内医学本科的，上学期间修了个统计硕士，也考过了那个USMLE，就是这边的执
照考试，但是申请住院医没有成功。现在也不知道这两个方向那个更适合。去做
programmer吧，是改行了，不是统计科班的；去做safety，我也没有执照，怕人
家不承认我这个外国的MD equivalent。 |
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e**p
发帖数: 4259 | 24 那你去试一试啊，就怕别人不给你这个没有经验的机会
给机会肯定能做的，当然做safety比programmer会有前途，但也得看个人兴趣还有能力
，比如说沟通，英文写作的能力
拿到了offer跟我说一声 |
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l*********g
发帖数: 94 | 26 确实是大多都要求经验的，可惜我没有。我申了好多，就一个回音要面试。有什么证可
以考来增加机会吗？万分感谢。 |
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h*****y
发帖数: 997 | 27 是个人都可以转SAS programmer， 不要轻易放弃你的医学背景！ |
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E*******s
发帖数: 994 | 29 please note this is a review article
topic: Recent Advances in Crowdsourcing for Biomedicine
keywords: crowdsourcing , mining crowd data, crowdsourced microtasking,
crowdsourced megatasking, pharmacovigilance, biocuration, structural biology
PhD preferred.
Please send a list of publications. |
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w********a
发帖数: 621 | 30 Application Support Engineer – Billerica, MA
• Provide technical support for group's deployed applications,
track statuses of incoming support issues, and ensure each is addressed in a
timely manner
• Diagnose and fix production application problems, coordinating
with Project Managers and Engineers where necessary
• Bachelor's degree or equivalent; 2+ years’ experience in an
application support role
• Experience debugging front end, web based applications such... 阅读全帖 |
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j*****7
发帖数: 4348 | 31 manager title doesn't necessarily means managerial duties, for example, in
some pharmaceutical companies, the entry level pharmacovigilance person's
title is manager, similarly, associate director in biostat normally manages
nobody but himself... It's not uncommon to see a 7 yrs exp stat PhD has an
AD title.
to |
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n*****n
发帖数: 57 | 32 http://en.wikipedia.org/wiki/Clinical_trial#Phases
Phase I
Phase I trials are the first stage of testing in human subjects. Normally, a
small (20-100) group of healthy volunteers will be selected. This phase
includes trials designed to assess the safety (pharmacovigilance),
tolerability, pharmacokinetics, and pharmacodynamics of a drug. These trials
are often conducted in an inpatient clinic, where the subject can be
observed by full-time staff. The subject who receives the drug is usually
obser |
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a*****e
发帖数: 2194 | 33 ◇◇新语丝(www.xys.org)(xys5.dxiong.com)(www.xinyusi.info)(xys2.dropin.org)
◇◇
方舟子究竟抄了没有？
作者：李福洋
http://blog.sciencenet.cn/u/GumpForrest
前一段时间，俺写了篇题目耸人听闻的科普博文《香烟是一种放射性核污
染!》，同一时间内，好像有南方的那个报纸也发表了相关话题的文章，这是后
来才知道的。有一天，俺看到一条评论：方舟子写了一篇从题目到内容都与此文
相似的文章，有抄袭之嫌吗？俺一看，第一反应是一阵惊喜：出名的机会可来了！
然后就顺着链接就去看了一下，是挺像，从一些表达方式，基本数据都能找到
“抄袭”的痕迹，可一看人家投稿时间，俺顿时泄气了，只能拿“英雄所见略同”
安慰自己了。看来俺是出名无望了。
这几天又有人指控方舟子抄袭，还整到什么法制周末了，好不热闹啊。俺也
凑凑热闹，趟趟浑水。【】是俺的评论。
....................................................................
.................. 阅读全帖 |
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h*******o
发帖数: 4884 | 34 I totally agree with you.
The ultimate goal of RA department in big pharmas is to make sure that their
products get to the market and stay in good shape in the market.
That is why RA is involved throughout the whole product life cycle.
From the very begining, RA is to make sure that all the manufacturing
process follow certain standard, either ISO standard for international/EU standard, or
21CFR 210 cGMP standard for drugs.
Then the product line moves to pre-clinical then, cGLP is the rule.
Afte... 阅读全帖 |
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H**********J
发帖数: 351 | 35 Primary Responsibilities and Accountabilities:
On the ED Core Team
• Represents medical science on ED Teams to
o ensure alignment on strategy between ED and LIP Criteria
o support target and clinical candidate selection (in collaboration with
Clinical Pharmacologist)
o provide guidance on benefit/risk assessment and risk mitigation
activities (responsibility shared with Clinical Pharmacologist)
• Is accountable for the overall design and the clinical and
scientific c... 阅读全帖 |
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h******e
发帖数: 1791 | 36 楼主大概不知道什么是pharmacovigilance。
4 |
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n*********s
发帖数: 552 | 37 拿不到学分，只是旁听，最后可以给一个certificate。泛泛而谈的话，我估计肯定是
有帮助的，问题是我现在很困难的权衡着。一边是由于个人原因终于有点时间想全心做
实验，发篇文章对自己博后生涯有个交代。另外一边，万一努力了还是到最后没有
publication，那就更难找工作，到时候如果想进industry，scientists估计没戏了，
如果上了这个课，指不准还能对找其它类工作有点帮助。问题是想把这个课
certificate拿到貌似还是要很多时间的，我肯定不能全心扑在实验上。所以想问一下
，尤其是industry的，我这种情况旁听这课的benefits是不是overweighing。唉，年纪
大了，家有小娃要养，没有时间造啊，每一个决定都小心翼翼～这课每周一次，两小时
，持续整个spring semester，schedule大概是这个样子：
Session 1 (Jan 22): Introduction to FDA and Forum for Collaborative HIV
Research
Session 2 (Jan 29): Standards for Eff... 阅读全帖 |
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c******h
发帖数: 4573 | 38 Life Science
RND00002290 (PhD Pharmacovigilance Manager)
RND00002297 (Clinical Veterinarian)
RND00002304 (PhD Sensory)
RND00002352 (PhD Human Safety Scientist / Toxicologist
Engineering
Physical Science / Other
RND00002291 (PhD Statistician – Cincinnati & Boston)
RND00002303 (PhD Scientist – Cincinnati)
RND00002332 (PhD Quantitative Scientist – Cincinnati)
RND00002351 (Post Doctoral Scientist/Engineer – Bethel)
RND00002364 (PhD Scientist – Cincinnati)
RND00002378 (PhD Method Deployment & Plant L... 阅读全帖 |
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d****y
发帖数: 2180 | 39 流行病学的话做 pharmacovigilence/pharmacology safety 最适合。 一般是上市的药
物安全性的监测。
有医学，流行病学博士学位，进大药厂应该还是可以的。懂一点统计的话就更吃香了。
药厂的话多种职位是可以考虑的，最好是research physician, 差一点research
scientist,从基层做起的话 research associate 之类的都可以。
回去工作还是有很多选择的。 国内三甲医院的医生生活也蛮滋润的。可能在二三线城
市的更舒服。 |
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h*******o
发帖数: 4884 | 40 that's wrong
Phase I is all about toxicity, or more specifically to find the maximal
tolerable dose with some Pk, Pd data collection. Usually no efficacy is
tested in phase I unless it's something like anti-cancer drugs.
Phase II is more about pk, pd and some efficacy.
Phase III is the large scale efficacy test.
Phase IV is about post market pharmacovigilence |
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T*******t
发帖数: 1069 | 41 various oncology positions open, great pay, benefit and job security,
contact me for details
Associate Biostatistics Director, Oncology
Associate Director, Clinical Studies
Associate Director, CPED Science, Oncology
Associate Director, Quality Assurance, R&D Programs, GCP
Associate Director, Regulatory Affairs
Clinical Research Specialist
Director, In Vivo Pharmacology
Director/Senior Director, Discovery
Global Development Project Leader, Oncology
Medical Director/Senior Medical Director, Oncolo... 阅读全帖 |
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j******w
发帖数: 97 | 42 Pharmacovigilence? Just my guess, not sure about the requirements though.
You can google it.
USA |
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l*********g
发帖数: 94 | 45 哦，涨知识了。那这两个方向上有哪些公认的证书课程么？ |
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b*****s
发帖数: 297 | 46 PV对中国人容易些，而且我觉得这帮人整天屁事没有。就搞点AE，半年搞一次，都是重
复性的，不要太轻松
★ 发自iPhone App: ChineseWeb 8.6 |
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l*********g
发帖数: 94 | 47 国内医学加本地公卫背景，没有医生执照。求职业发展建议，多谢懂行的前辈指点。 |
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p**y
发帖数: 170 | 48 这两个没有经验很难入行吧。你也许考虑下healthcare economics outcomes research
? |
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l*********g
发帖数: 94 | 49 outcome research 我觉得有点水。我现在就在CRO里，就是想找个最适合学医背景的方
向发展。
research |
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w****b
发帖数: 777 | 50
outcome research 有点水?????
请问你有什么资格这么说？ |
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