j******8
发帖数: 12 | 1 We are working with a top Multinational Pharmacy Company to recruit Clinical
Pharmacologist for their R&D center in China (Beijing or Shanghai),
especially in Phase 1/Clinical Pharmacology/PK/PD studies and Clinical
Pharmacology strategy. This position belongs to Early Research Development
Department.
Here’s the JD of this position:
Primary Responsibilities:
• Both build new and apply known disease and drug models as stated
previously. This will be based on clinical trial information inside Roche as
well as the literature
• Design and analyze cross-trial pharmacokinetic-pharmacodyamic
analysis to understand who responds to treatment and who is exposed to risk.
• Simulate new situations (e.g., trial design, efficacy-safety in
new populations) based on prior data and models.
• Provide quantitative analysis for the Asia-Pacific market
including dose-response, trial design, dosage form performance and new
patient subpopulations (e.g., pedatrics, elderly)
• Provide Clinical Pharmacology expertise to p-RED project teams
for drug candidates discovered by China R&D.
• Evaluate understand pre-clinical package data for EIH studies,
design, conduct, analyze SD and MD EIH studies and mechanism of action
studies) .
• Provide local China and other Asia Pacific Countries, clinical
pharmacology input for local Phase I/II support for global projects and
Lifecycle Teams.
• Serve as a China liaison with Global Clinical Pharmacologist for
the assigned projects.
• Lead or contribute to cross-functional working groups in the
context of project teams
and/or clinical pharmacology activities.
• Develop the timely, scientifically sound, business-required
clinical pharmacology studies to support early stage (Phase I-II) and late-
stage studies or NDA approvals in China and other Asia Pacific Countries.
• Prepare in a timely manner and with high quality the relevant
documentation (protocols and amendments, CSRs), or the clinical pharmacology
component of other high level
documents such as INDs, IDBs, NDA/PLA expert reports, Chinese package
inserts).
• Deliver high-quality evaluation and interpretation of clinical
pharmacology data
(pharmacokinetics, pharmaco-dynamics, safety, dose/concentration response).
• Interact with investigators with regard to scientific issues.
• Be responsible for the integrity of Clinical Pharmacology studies
conducted by p-RED.
from protocol design, execution, data analysis and final study report
perspective is at the best global level.
• Adopt efficient and effective global local clinical pharmacology
study working process and experience and implement them in China, in
alignment with the global organization
(p-RED).
• Deliver portions of the NDA documentation, responses to Asia
Pacific Regulatory
Agencies questions, and preparation of materials for use in presentation,
for all
interactions with regulatory authorities with regards to clinical
pharmacology issues.
• Contributes to appropriate budget and manpower planning for the
assigned activities.
• Prepare or contributes to primary publications for the assigned
products.
• Support the assigned product during the launch phase as demanded
by the business
organizations.
• Provide technical coaching and mentoring to the junior
scientists to grow in the field of
Clinical Pharmacology or Clinical Pharmacology studies.
• If deemed appropriate, providing group lectures, individual
coaching or constructive
feedback to colleagues who are new to the concept of Clinical Pharmacology
in Asia-
Pacific project teams.
• Interact with pre-clinical research and development scientists
in China or in Global to
provide reliable clinical pharmacology expertise and advice to the research
teams in China and AP.
• Participate in evaluation of the Clinical Pharmacology Unit or
Clinical Pharmacology
CROs, if needed.
• Provide support to train Data Managers, PK/PD Lab managers,
Clinical Monitors for the
Clinical Pharmacology studies.
• Participate and represent clinical pharmacology on due diligence
team
• Participate and contribute to the ED &CP Asia Pacific or Global
Department initiatives.
Qualification and Experience:
Minimum:
• PharmD, PhD, or MD in clinical pharmacology, or an area relevant
to clinical
pharmacology, with relevant 8 years clinical and pharmaceutical industry
experience in the
planning and conduct of clinical trials (preferably early human studies in a
pharmaceutical industry setting).
• Relevant expertise in nonlinear mixed effects modeling of
clinical trial data focused on population PK-PD modeling
• Demonstrated ability to conceive, plan, conduct and analyze
sparse samples related to efficacy and safety
• Demonstrated ability to analyze high intensity phase 1 -2 PK-PD
trials for dose selection
• Publication of these studies in peer reviewed journals
• Appropriate computer software experience (including WINNONLIN or
other similar PK
analysis tool, MS Word, Excel, PowerPoint, etc).
• In-depth knowledge of the global drug development process.
• Capability to learning the China regulatory requirement and
process.
• Able to represent Roche interact with regulatory authorities.
• Hands on approach to daily work.
• Able to work in a quickly changing, not fully structured internal
and external environment
Kind regards,
Jane Lee 李艳
HR Consultant
GEN Enterprise Management Consulting Co., Ltd.
Tel：+86 21 5155 8084 ext 839 Email：j****[email protected] | j******8
发帖数: 12 | 2 没人跟帖呀？哎。同学们，帮忙转转哈~职位级别蛮高，薪酬可谈空间也大。
顺便说下今年罗氏Early Development招聘人数82人；海外做完博士后的就行。欢迎回
国哈O(∩_∩)O | b**u
发帖数: 2761 | 3 还要做完博后才行啊？哪方面的？
我有朋友在找国内的工作。
【在 j******8 的大作中提到】
: 没人跟帖呀？哎。同学们，帮忙转转哈~职位级别蛮高，薪酬可谈空间也大。
: 顺便说下今年罗氏Early Development招聘人数82人；海外做完博士后的就行。欢迎回
: 国哈O(∩_∩)O
| b**u
发帖数: 2761 | 4 看来回国做scientist比在美国做scientist难多了。
【在 j******8 的大作中提到】
: 没人跟帖呀？哎。同学们，帮忙转转哈~职位级别蛮高，薪酬可谈空间也大。
: 顺便说下今年罗氏Early Development招聘人数82人；海外做完博士后的就行。欢迎回
: 国哈O(∩_∩)O
| b******e
发帖数: 3348 | 5 国内比国外更难啊，哎。
【在 j******8 的大作中提到】
: 没人跟帖呀？哎。同学们，帮忙转转哈~职位级别蛮高，薪酬可谈空间也大。
: 顺便说下今年罗氏Early Development招聘人数82人；海外做完博士后的就行。欢迎回
: 国哈O(∩_∩)O
| y**g
发帖数: 197 | 6 工业界为什么要postdoc?找不到工作或者要换个方向才会做吧。 | j******w
发帖数: 97 | 7 扫了一眼 job description.感觉中国人做clinical pharmacology 的不多。有8年工
作经验的更少。而且这个工作很偏clincal trial design. 有这个背景的在美国应该也
有不错的工作。想回去的更少。
Clinical
stated
as
【在 j******8 的大作中提到】
: We are working with a top Multinational Pharmacy Company to recruit Clinical
: Pharmacologist for their R&D center in China (Beijing or Shanghai),
: especially in Phase 1/Clinical Pharmacology/PK/PD studies and Clinical
: Pharmacology strategy. This position belongs to Early Research Development
: Department.
: Here’s the JD of this position:
: Primary Responsibilities:
: • Both build new and apply known disease and drug models as stated
: previously. This will be based on clinical trial information inside Roche as
: well as the literature
| f********e
发帖数: 2194 | 8 那工作几年的呢？也是senior scientist？
【在 j******8 的大作中提到】
: 没人跟帖呀？哎。同学们，帮忙转转哈~职位级别蛮高，薪酬可谈空间也大。
: 顺便说下今年罗氏Early Development招聘人数82人；海外做完博士后的就行。欢迎回
: 国哈O(∩_∩)O
| y**g
发帖数: 197 | 9 我觉的你写的这些大半都是preclinical, not clinical pharmacology。 8年！
clinical pk/pd升职很快的，3，4年就可以成director级的.另外中国人做clinical pk
的很多。至少我见的abbott, pfizer,norvatis and j&j 1/4都是中国人. merck dmpk
好多中国女同胞。不过大头老美多。clinical pk 一半时间是开会，耍嘴皮，难度比较
低。你的要求是senior director 级的。条件不够！！ | b**u
发帖数: 2761 | 10 其实这个title也没那么重要，不同公司给entry level phd的title有的有scientist,
也有sr scientist, 也有principal scientist。
貌似很多大公司给的是sr scientist。
【在 j******8 的大作中提到】
: 没人跟帖呀？哎。同学们，帮忙转转哈~职位级别蛮高，薪酬可谈空间也大。
: 顺便说下今年罗氏Early Development招聘人数82人；海外做完博士后的就行。欢迎回
: 国哈O(∩_∩)O
| | | b******e
发帖数: 3348 | 11 这个sr是什么意思呢
,
【在 b**u 的大作中提到】
: 其实这个title也没那么重要，不同公司给entry level phd的title有的有scientist,
: 也有sr scientist, 也有principal scientist。
: 貌似很多大公司给的是sr scientist。
| w******r
发帖数: 3156 | 12 senior
楼上有人说3-4年升到director, 我觉得没那么快，有的公司到associate director有
可能，到director我觉得不容易。
【在 b******e 的大作中提到】
: 这个sr是什么意思呢
:
: ,
| b**u
发帖数: 2761 | 13 国内的话有可能吧，好象很多人的title都是director,中文好象主任也翻译成director
.呵呵
【在 w******r 的大作中提到】
: senior
: 楼上有人说3-4年升到director, 我觉得没那么快，有的公司到associate director有
: 可能，到director我觉得不容易。
| b**u
发帖数: 2761 | 14 呵呵，做pk的貌似就是女的做的多一些。我个人感觉哈，没什么具体数据支持，哈哈。
pk
dmpk
【在 y**g 的大作中提到】
: 我觉的你写的这些大半都是preclinical, not clinical pharmacology。 8年！
: clinical pk/pd升职很快的，3，4年就可以成director级的.另外中国人做clinical pk
: 的很多。至少我见的abbott, pfizer,norvatis and j&j 1/4都是中国人. merck dmpk
: 好多中国女同胞。不过大头老美多。clinical pk 一半时间是开会，耍嘴皮，难度比较
: 低。你的要求是senior director 级的。条件不够！！
| w******r
发帖数: 3156 | 15 show me the data 哈哈
我也觉得女的略多一些，至少中国人是这样
【在 b**u 的大作中提到】
: 呵呵，做pk的貌似就是女的做的多一些。我个人感觉哈，没什么具体数据支持，哈哈。
:
: pk
: dmpk
| y**g
发帖数: 197 | 16 我指的是Merck 的 DMPK，有很多女的。其它公司有但比例不大。因为DMPK做实验分析
啥的。各个公司title不一样，3-5年的是低级的director. | b**u
发帖数: 2761 | 17 "东北尤其出医药人才~"你这是要挑起地域之争ha，南药沈药，南方北方都有医药人才
呀。
这个版上的南药人不少的。
btw, 你这个职位是哪个药厂？直接报上名字吧。
【在 j******8 的大作中提到】
: 没人跟帖呀？哎。同学们，帮忙转转哈~职位级别蛮高，薪酬可谈空间也大。
: 顺便说下今年罗氏Early Development招聘人数82人；海外做完博士后的就行。欢迎回
: 国哈O(∩_∩)O
| b**u
发帖数: 2761 | 18 show you the data? 我做过pk，当时组里5个人全是女的。
【在 w******r 的大作中提到】
: show me the data 哈哈
: 我也觉得女的略多一些，至少中国人是这样
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