s*****9
发帖数: 285 | 1 大家好，我现在手上有一些PHARM大公司一些CONTRACTOR POSITIONS, 我想找些大学／
MS刚毕业，统计背景为佳的人，有兴趣把你简历发给我，s*******[email protected]，我需
要收取的TRIANING的费用，不过一部分可以在你找到工作以后在分期给我，刚刚开始做
所以很多东西都在实验阶段。
OPT为佳，我不是公司，不帮你SPONSOR，不过技术关过了，N多个大公司会帮你SPONSOR
，我知道现在找工作的人很多，你们别把我邮箱挤暴了。
需要QUALIFICATION：
１。SAS统计背景，电脑操作性很强者为佳
２。英文表达能力强
３。DC附近比较好，其他州的同学你们必须自己开车过来找房子。
4。性格稍微好点的，我教人的时候你假如都教不会脾气比较爆，不过我人很好，比较
容易交流。
把你的简历和联系方式发到我的邮箱，我觉得合适我会挂给你给你TECHNICAL PHONE
SCREEN。
顺便提一下我的最高记录，一次拿了３个OFFER，可能RECRUITOR多点，应该都更成功，， | s*****9
发帖数: 285 | 2 这两天有收到RECRUITOR的分别为ABBOTT（IL），PFIZER（NJ），EDWARD LAB（CA），
我还会加强下我跟RECRUITOR的联系，TRAINING主要负责你技术和面试这一块,需要时间保守估计是２个月左右，因为我现在在单位上班，所以也只能下班以后上２－３个小时的课程，然后你自己做PRESENTATION，就住在DC的朋友可以约出来详细了解下假如有任何问题,以前和我一起TRAIN的朋友现在有在BMS，CDC，ALLERGEN工作的,重申一下我不是一个公司，不是ICC，是个人１对１的TRAINING，估计最多也招不会超过３个人，我精力毕竟有限. | s*****9
发帖数: 285 | 3 BL，需要增加一个你的PRESENTATION SKILLS，口音有问题不是问题，但是最主要你的
重点要讲到，要抓住JOB DESCRIPTION而去展开讲你的PROJECT，少说学历，你离我太远
了，还是不是非常的适合，没关系，有什么关于面试的问题尽管可以问我，而且我听说你也是
拖家带口的，BUENO SUERTE, ，好好努力,昨天不好意思，陪个女生去MALL，：D | s*****9
发帖数: 285 | | s*****9
发帖数: 285 | 5 需要一个好的６年经验的SR SAS PROGRAMMER做一个３个月的CONTRACT，PAY很高。
The Statistical Analyst provides work direction and training for 0-3 Sr./
Statistical Programmers and for 0-3 contract programmers. Supervise and
provide SAS programming support to statistics and clinical teams.
Participate in decision making on a departmental basis on the topics of
global database design and structure, as well as, statistical programming
issues.
Responsibilities include:
1. SAS Programming support includes but is not limited to (a) the creation
of statistical and medical tables and data listings which are an integral
part of the individual study reports submitted to the FDA, (b) the creation
of case report form tabulations and other customized data sets and output
which are supplied to the FDA in place of the original case report forms, (c
) the creation of ad hoc reports per requests by statistics or clinical
teams to aid in the analysis or review of clinical data, and (d) the
creation of specialized data sets to be used by internal and external groups.
2. Collaborative working relationships with statistics, data management,
clinical teams and personnel from other companies to communication project
status, resolve issues and determine study/project standards.
3. Work with data management and statistics to achieve consistency and
acceptability in the database structure and design. Review and sign off CRFs
and database specifications.
4. Maintain expertise in the use of UNIX utilities and SAS macros
specifically developed for the section and continue development of such
utilities/macros to improve process, as well as presenting information on
the utilities/macros and maintaining documentation on them.
5. Assure that all programs for a project meet the current section standards
, are consistent in terms of format/style and are documented appropriately.
6. Assure the accuracy of all programs for a project by reviewing listing
and log files and running all checking utilities.
7. Oversee the work of assigned Sr./Statistical Programmers and contractors
and ascertain that the work meets all pertinent standards as noted above.
Participates in Client planning on assigned projects. Effectively adapt to
and assume the many technical, supervisory and administrative
responsibilities.
8. Provide technical support and training to study programmers.
9. Continue technical and personal development in the areas of database
design, programming issues and understanding the data from a medical,
statistical and computer programming viewpoint.
10. Provide consulting services for statisticians who program in SAS.
11. Participate in the discussions on global database design and structure.
12. Develop training documents for new study programmers.
13. Responsible for identifying opportunities for productivity improvements
and formulating implementation plans.
14. Work with Statisticians and Clinicians to come up with design
specifications for non-standard tables and listings required for a study.
Participate and contribute to discussions regarding statistical methods to
be utilized.
Education
Must have a Bachelor degree in physical, mathematical, or computer science
or related field or equivalent. A Masters Degree is preferred.
6+ years of related experience with demonstrated excellent skills/
accomplishments as a Statistical Programmer or equivalent. A comprehensive
understanding of clinical trials database design and structure along with a
fundamental knowledge of statistical programming issues is required.
| s*****9
发帖数: 285 | 6 ABBOTT钱不是很多，CONTRACT２HIRE，２轮PHONE SCREEN，第一轮我面过，感觉还行。
Clinical Statistician I – B ABLJP00027218
Abbott Labs
Abbott Park, IL 60064
8 – 12/2011
Experience in database management (preferably claims and other healthcare
databases), SAS programming and analysis skills are also a plus. Understands
and appropriately uses advanced epidemiological research techniques: •
;Understands primary and secondary research techniques as well as the
elements of more complex quantitative research methods, statistical
programming and multiple study designs. •Broad knowledge of public and
private resources and databases relevant to epidemiology and their use in
testing and supporting hypotheses and making recommendations •
Experience in contributing to the writing and publishing of scientific
articles, presentations and posters •Plays role in protocol
development, questionnaire design and statistical analysis plan for primary
research •Experienced in independent analysis of data from
epidemiology studies and comprehension of epidemiology literature Experience
in managing small numbers of research analysts and/or staff Computer
proficient (Windows, Word, Excel, Access, SAS and Endnote) Some ability to
initiate quantitative methodology to answer research questions Knowledge of
pharmaceutical safety databases and AE reporting conventions Some
understanding of surveillance & safety evaluation including signal detection
Ability to manage multiple and more complex projects within several
therapeutic areas Ability to present complex scientific data clearly to
groups with varying levels of epidemiology experience as well as upper
management Ability to collaborate effectively and serve as a resource to
colleagues and other teams
Successful candidates should possess an MPH with 5 or more years of
epidemiology and /or surveillance-related industry experience. An advanced
degree in biostatistics would also be considered.
Clinical Statistician ABLJP00026950
Abbott Park, IL
8/2011 – 1/2012
Provide statistical expertise for study case report for design, data base
structure, analysis plan, and review of the study protocols and reports.
Perform data analysis and provide statistical support including
collaboration with medical groups to complete joint scientific reports and
FDA overviews, including review of such reports to ensure accuracy and
clarity. Must have clinical research experience.
3-5 Years Experience Level.
Master's Degree required. Prior pharma exp strongly preferred
Clinical Statistian ABLJP00026386
Abbott Park, IL
8/2011 – 12/2012
Provide statistical expertise for study case report for design, data base
structure, analysis plan, and review of the study protocols and reports.
Perform data analysis and provide statistical support including
collaboration with medical groups to complete joint scientific reports and
FDA overviews, including review of such reports to ensure accuracy and
clarity. Must have clinical research experience. 3-5 Years Experience Level. | s*****9
发帖数: 285 | 7 GSk的RATE也算比较SENIOR的，ENTRY－LEVEL的RESUME应该比较难上，有SENIOR有兴趣
给我RESUME
Raleigh (Research Triangle Park) position at GSK (Glaxo)
Clinical Programmer Analyst
Providing technical support and assistance to clinical study teams, enabling
them to deliver high quality clinical trial data. This role is centered
around the extraction, manipulation and reporting of eCRF and non-eCRF data,
with a close linkage to the development, deployment and maintenance of the
eCRF data capture package. A working knowledge of GCP and its impact in the
clinical data acquisition domain is required. A track record of successfully
working with SAS for data quality checking and data manipulation is
required, and experience with other tools such as Oracle’s InForm Architect
tool (version 4.6), VB Script, PL/SQL, SQL, COGNOS, XML is strongly
preferred. Demonstrated ability of successfully communicating complex
technical issues to a non-technical audience as well as demonstrated ability
of managing multiple deliverables to time and quality. Ability to focus on
customer needs, troubleshooting, and providing innovative technical
solutions, while adhering to standards. | s*****9
发帖数: 285 | 8 ABBOTT还有一个POSITION OPENING，需要的人跟我联系，最好不要FRESH－MASTER的 | h******s
发帖数: 3420 | 9 这种位置啥叫高？啥叫还可以？
听说是40起价的吧，5，60都算一般吧
【在 s*****9 的大作中提到】
: 需要一个好的６年经验的SR SAS PROGRAMMER做一个３个月的CONTRACT，PAY很高。
: The Statistical Analyst provides work direction and training for 0-3 Sr./
: Statistical Programmers and for 0-3 contract programmers. Supervise and
: provide SAS programming support to statistics and clinical teams.
: Participate in decision making on a departmental basis on the topics of
: global database design and structure, as well as, statistical programming
: issues.
: Responsibilities include:
: 1. SAS Programming support includes but is not limited to (a) the creation
: of statistical and medical tables and data listings which are an integral
| s*****9
发帖数: 285 | 10 90-100 ba, SF BAY
【在 h******s 的大作中提到】
: 这种位置啥叫高？啥叫还可以？
: 听说是40起价的吧，5，60都算一般吧
| | | h******s
发帖数: 3420 | 11 Crazy
cs 的也就7，80
【在 s*****9 的大作中提到】
: 90-100 ba, SF BAY
| s*****9
发帖数: 285 | | N****n
发帖数: 1208 | 13 你一次说完吧。。。。磨磨唧唧的。。。
版上的都是交流学术，面试完友情提供面经经验的。
你这个新ID，不说自己的背景，上来就打广告挣钱，还“别把我邮箱挤爆了” 。。。
。。。。。。
enabling
data,
the
the
【在 s*****9 的大作中提到】
: GSk的RATE也算比较SENIOR的，ENTRY－LEVEL的RESUME应该比较难上，有SENIOR有兴趣
: 给我RESUME
: Raleigh (Research Triangle Park) position at GSK (Glaxo)
: Clinical Programmer Analyst
: Providing technical support and assistance to clinical study teams, enabling
: them to deliver high quality clinical trial data. This role is centered
: around the extraction, manipulation and reporting of eCRF and non-eCRF data,
: with a close linkage to the development, deployment and maintenance of the
: eCRF data capture package. A working knowledge of GCP and its impact in the
: clinical data acquisition domain is required. A track record of successfully
| s*****9
发帖数: 285 | 14 不怪你，你看到的毕竟只是行业的冰山一角，我的工作机会还有继续增加，假如你够资
深，你根本可以自己找，或者把简历给我，我给你机会，广告只是留给那些希望进入行
业的人的，面经只是一个而且，面到后面真正有经验的就根本不用准备了，已经有不少
人接受我的帮助了，我不需要在解释我的动机.我才刚开始工作，希望能架起一座桥梁
帮助那些需要帮助的别人。
【在 N****n 的大作中提到】
: 你一次说完吧。。。。磨磨唧唧的。。。
: 版上的都是交流学术，面试完友情提供面经经验的。
: 你这个新ID，不说自己的背景，上来就打广告挣钱，还“别把我邮箱挤爆了” 。。。
: 。。。。。。
:
: enabling
: data,
: the
: the
| s*****9
发帖数: 285 | | s*****9
发帖数: 285 | 16 最近还有个中国人在DC边上和FDA有个PROJECT，是在他公司的员工，在FDA干活，他说H
１B SPONSOR钱对半出。过几天和他喝下咖啡，看看具体怎么样。还是要懂CDISC的东西,附上JOB DESCRIPTION
Demonstrated experience in SAS programming in health care environment, preferably in the creation of clinical trial analysis datasets
Excellent communication and interpersonal skills
Hands-on programming with SAS v9 or above, S-Plus and R
Experience and Knowledge in a medical research environment, meta-analysis, and publication in biostatistical and biomedical journals
With hands-on experience in clinical trails to create analysis dataset with specific structure according to the more up-to-date Clinical Data Interchange Standards Consortium (CDISC) standard
Create a unified analysis dataset in CDISC-ADaM format for studies from source datasets
Derive requested variables from studies
Validate the derive dataset with proposed Qulity Control Procedure Plan and compare with the original source data
Convert source data from selected studies to CDISC SDTM with unified data structure
Conduct exploratory and meta-data analysis and prepare reports
Identify statistical methodology issues
Phd or master degree in statistics/biostatistics | s*****9
发帖数: 285 | 17 要ISS和ISE的，我是不会，有会的就来吧。。。
Job Description:
Contribute to computer programming efforts for a clinical trial drug project
and to provide programming support for clinical trial data reporting and
regulatory submissions. Assumes protocol level and some project management
responsibility while supporting the Programming and Statistics lead. Able to
support multiple protocols independently and to contribute to integrated
summaries of efficacy and safety. Demonstrates strong SAS programming skills
; participates in protocol team and some project team interactions. Builds
successful relationships and seamless interfaces at the protocol/project
team level. Provides timely and effective communication to the programming
and statistics leads. | s*****9
发帖数: 285 | 18 Job Title: Statistical Programmer II
City/State:Florham Park, NJ
Assignment Duration: 6 months w/ expected renew
One of our clients in Florham Park, NJ is seeking a Statistical Programmer
II to join their team immediately.
6 month assignment
" Provide statistical programming support and validation and help set
specifications of analysis datasets, pooled datasets, statistical tables,
summaries, figures and listing for Phase II-IV clinical trials.
" Employ standardized programs where applicable.
" Provide input into planning documents such as protocol, validation
plan, and report analysis plan. Provide outputs for clinical study reports,
integrated summaries and electronic submissions.
" Help respond to health authority inquiries for submitted dossiers.
" Establish and maintain sound working relationship and effective
communications within biostatistics and statistical reporting and clinical
research.
Education/Experience:
1-2 years of Analytical experience.
BA/BS or equivalent experience in computer science, mathematics, statistics,
life sciences, or related field(s). Intermediate SAS programming skills,
with 2-5 years experience in a medical setting, preferably working with
clinical trial data. Good understanding of clinical trial practices,
procedures and methodologies. Good verbal and written communication skills.
Good interpersonal and organizational skills. Attention to detail and
correctness. Working knowledge of office tools | s*****9
发帖数: 285 | 19 FDA OFFER被我REFER过去的哥们拿到了，先摘下来了，有兴趣加入的朋友下次会给你们
CONFERENCE下，给告诉下他的心得。 | d****z
发帖数: 301 | 20 同志们, 什么叫ICC, 这个就是. slian59: 你敢说不要改假简历么?
请版主把他封了吧 | | | s*****9
发帖数: 285 | 21 不改简历，改下你做的PROJECTS,丰满一点就可以了，用假名和用假工作经历没必要。 | s*****9
发帖数: 285 | 22 大家好，我现在手上有一些PHARM大公司一些CONTRACTOR POSITIONS, 我想找些大学／
MS刚毕业，统计背景为佳的人，有兴趣把你简历发给我，s*******[email protected]，我需
要收取的TRIANING的费用，不过一部分可以在你找到工作以后在分期给我，刚刚开始做
所以很多东西都在实验阶段。
OPT为佳，我不是公司，不帮你SPONSOR，不过技术关过了，N多个大公司会帮你SPONSOR
，我知道现在找工作的人很多，你们别把我邮箱挤暴了。
需要QUALIFICATION：
１。SAS统计背景，电脑操作性很强者为佳
２。英文表达能力强
３。DC附近比较好，其他州的同学你们必须自己开车过来找房子。
4。性格稍微好点的，我教人的时候你假如都教不会脾气比较爆，不过我人很好，比较
容易交流。
把你的简历和联系方式发到我的邮箱，我觉得合适我会挂给你给你TECHNICAL PHONE
SCREEN。
顺便提一下我的最高记录，一次拿了３个OFFER，可能RECRUITOR多点，应该都更成功，， | s*****9
发帖数: 285 | 23 这两天有收到RECRUITOR的分别为ABBOTT（IL），PFIZER（NJ），EDWARD LAB（CA），
我还会加强下我跟RECRUITOR的联系，TRAINING主要负责你技术和面试这一块,需要时间保守估计是２个月左右，因为我现在在单位上班，所以也只能下班以后上２－３个小时的课程，然后你自己做PRESENTATION，就住在DC的朋友可以约出来详细了解下假如有任何问题,以前和我一起TRAIN的朋友现在有在BMS，CDC，ALLERGEN工作的,重申一下我不是一个公司，不是ICC，是个人１对１的TRAINING，估计最多也招不会超过３个人，我精力毕竟有限. | s*****9
发帖数: 285 | 24 BL，需要增加一个你的PRESENTATION SKILLS，口音有问题不是问题，但是最主要你的
重点要讲到，要抓住JOB DESCRIPTION而去展开讲你的PROJECT，少说学历，你离我太远
了，还是不是非常的适合，没关系，有什么关于面试的问题尽管可以问我，而且我听说你也是
拖家带口的，BUENO SUERTE, ，好好努力,昨天不好意思，陪个女生去MALL，：D | s*****9
发帖数: 285 | 25 需要一个好的６年经验的SR SAS PROGRAMMER做一个３个月的CONTRACT，PAY很高。
The Statistical Analyst provides work direction and training for 0-3 Sr./
Statistical Programmers and for 0-3 contract programmers. Supervise and
provide SAS programming support to statistics and clinical teams.
Participate in decision making on a departmental basis on the topics of
global database design and structure, as well as, statistical programming
issues.
Responsibilities include:
1. SAS Programming support includes but is not limited to (a) the creation
of statistical and medical tables and data listings which are an integral
part of the individual study reports submitted to the FDA, (b) the creation
of case report form tabulations and other customized data sets and output
which are supplied to the FDA in place of the original case report forms, (c
) the creation of ad hoc reports per requests by statistics or clinical
teams to aid in the analysis or review of clinical data, and (d) the
creation of specialized data sets to be used by internal and external groups.
2. Collaborative working relationships with statistics, data management,
clinical teams and personnel from other companies to communication project
status, resolve issues and determine study/project standards.
3. Work with data management and statistics to achieve consistency and
acceptability in the database structure and design. Review and sign off CRFs
and database specifications.
4. Maintain expertise in the use of UNIX utilities and SAS macros
specifically developed for the section and continue development of such
utilities/macros to improve process, as well as presenting information on
the utilities/macros and maintaining documentation on them.
5. Assure that all programs for a project meet the current section standards
, are consistent in terms of format/style and are documented appropriately.
6. Assure the accuracy of all programs for a project by reviewing listing
and log files and running all checking utilities.
7. Oversee the work of assigned Sr./Statistical Programmers and contractors
and ascertain that the work meets all pertinent standards as noted above.
Participates in Client planning on assigned projects. Effectively adapt to
and assume the many technical, supervisory and administrative
responsibilities.
8. Provide technical support and training to study programmers.
9. Continue technical and personal development in the areas of database
design, programming issues and understanding the data from a medical,
statistical and computer programming viewpoint.
10. Provide consulting services for statisticians who program in SAS.
11. Participate in the discussions on global database design and structure.
12. Develop training documents for new study programmers.
13. Responsible for identifying opportunities for productivity improvements
and formulating implementation plans.
14. Work with Statisticians and Clinicians to come up with design
specifications for non-standard tables and listings required for a study.
Participate and contribute to discussions regarding statistical methods to
be utilized.
Education
Must have a Bachelor degree in physical, mathematical, or computer science
or related field or equivalent. A Masters Degree is preferred.
6+ years of related experience with demonstrated excellent skills/
accomplishments as a Statistical Programmer or equivalent. A comprehensive
understanding of clinical trials database design and structure along with a
fundamental knowledge of statistical programming issues is required.
| s*****9
发帖数: 285 | 26 ABBOTT钱不是很多，CONTRACT２HIRE，２轮PHONE SCREEN，第一轮我面过，感觉还行。
Clinical Statistician I – B ABLJP00027218
Abbott Labs
Abbott Park, IL 60064
8 – 12/2011
Experience in database management (preferably claims and other healthcare
databases), SAS programming and analysis skills are also a plus. Understands
and appropriately uses advanced epidemiological research techniques: •
;Understands primary and secondary research techniques as well as the
elements of more complex quantitative research methods, statistical
programming and multiple study designs. •Broad knowledge of public and
private resources and databases relevant to epidemiology and their use in
testing and supporting hypotheses and making recommendations •
Experience in contributing to the writing and publishing of scientific
articles, presentations and posters •Plays role in protocol
development, questionnaire design and statistical analysis plan for primary
research •Experienced in independent analysis of data from
epidemiology studies and comprehension of epidemiology literature Experience
in managing small numbers of research analysts and/or staff Computer
proficient (Windows, Word, Excel, Access, SAS and Endnote) Some ability to
initiate quantitative methodology to answer research questions Knowledge of
pharmaceutical safety databases and AE reporting conventions Some
understanding of surveillance & safety evaluation including signal detection
Ability to manage multiple and more complex projects within several
therapeutic areas Ability to present complex scientific data clearly to
groups with varying levels of epidemiology experience as well as upper
management Ability to collaborate effectively and serve as a resource to
colleagues and other teams
Successful candidates should possess an MPH with 5 or more years of
epidemiology and /or surveillance-related industry experience. An advanced
degree in biostatistics would also be considered.
Clinical Statistician ABLJP00026950
Abbott Park, IL
8/2011 – 1/2012
Provide statistical expertise for study case report for design, data base
structure, analysis plan, and review of the study protocols and reports.
Perform data analysis and provide statistical support including
collaboration with medical groups to complete joint scientific reports and
FDA overviews, including review of such reports to ensure accuracy and
clarity. Must have clinical research experience.
3-5 Years Experience Level.
Master's Degree required. Prior pharma exp strongly preferred
Clinical Statistian ABLJP00026386
Abbott Park, IL
8/2011 – 12/2012
Provide statistical expertise for study case report for design, data base
structure, analysis plan, and review of the study protocols and reports.
Perform data analysis and provide statistical support including
collaboration with medical groups to complete joint scientific reports and
FDA overviews, including review of such reports to ensure accuracy and
clarity. Must have clinical research experience. 3-5 Years Experience Level. | s*****9
发帖数: 285 | 27 GSk的RATE也算比较SENIOR的，ENTRY－LEVEL的RESUME应该比较难上，有SENIOR有兴趣
给我RESUME
Raleigh (Research Triangle Park) position at GSK (Glaxo)
Clinical Programmer Analyst
Providing technical support and assistance to clinical study teams, enabling
them to deliver high quality clinical trial data. This role is centered
around the extraction, manipulation and reporting of eCRF and non-eCRF data,
with a close linkage to the development, deployment and maintenance of the
eCRF data capture package. A working knowledge of GCP and its impact in the
clinical data acquisition domain is required. A track record of successfully
working with SAS for data quality checking and data manipulation is
required, and experience with other tools such as Oracle’s InForm Architect
tool (version 4.6), VB Script, PL/SQL, SQL, COGNOS, XML is strongly
preferred. Demonstrated ability of successfully communicating complex
technical issues to a non-technical audience as well as demonstrated ability
of managing multiple deliverables to time and quality. Ability to focus on
customer needs, troubleshooting, and providing innovative technical
solutions, while adhering to standards. | s*****9
发帖数: 285 | 28 ABBOTT还有一个POSITION OPENING，需要的人跟我联系，最好不要FRESH－MASTER的 | h******s
发帖数: 3420 | 29 这种位置啥叫高？啥叫还可以？
听说是40起价的吧，5，60都算一般吧
【在 s*****9 的大作中提到】
: 需要一个好的６年经验的SR SAS PROGRAMMER做一个３个月的CONTRACT，PAY很高。
: The Statistical Analyst provides work direction and training for 0-3 Sr./
: Statistical Programmers and for 0-3 contract programmers. Supervise and
: provide SAS programming support to statistics and clinical teams.
: Participate in decision making on a departmental basis on the topics of
: global database design and structure, as well as, statistical programming
: issues.
: Responsibilities include:
: 1. SAS Programming support includes but is not limited to (a) the creation
: of statistical and medical tables and data listings which are an integral
| s*****9
发帖数: 285 | 30 90-100 ba, SF BAY
【在 h******s 的大作中提到】
: 这种位置啥叫高？啥叫还可以？
: 听说是40起价的吧，5，60都算一般吧
| | | h******s
发帖数: 3420 | 31 Crazy
cs 的也就7，80
【在 s*****9 的大作中提到】
: 90-100 ba, SF BAY
| s*****9
发帖数: 285 | | N****n
发帖数: 1208 | 33 你一次说完吧。。。。磨磨唧唧的。。。
版上的都是交流学术，面试完友情提供面经经验的。
你这个新ID，不说自己的背景，上来就打广告挣钱，还“别把我邮箱挤爆了” 。。。
。。。。。。
enabling
data,
the
the
【在 s*****9 的大作中提到】
: GSk的RATE也算比较SENIOR的，ENTRY－LEVEL的RESUME应该比较难上，有SENIOR有兴趣
: 给我RESUME
: Raleigh (Research Triangle Park) position at GSK (Glaxo)
: Clinical Programmer Analyst
: Providing technical support and assistance to clinical study teams, enabling
: them to deliver high quality clinical trial data. This role is centered
: around the extraction, manipulation and reporting of eCRF and non-eCRF data,
: with a close linkage to the development, deployment and maintenance of the
: eCRF data capture package. A working knowledge of GCP and its impact in the
: clinical data acquisition domain is required. A track record of successfully
| s*****9
发帖数: 285 | 34 不怪你，你看到的毕竟只是行业的冰山一角，我的工作机会还有继续增加，假如你够资
深，你根本可以自己找，或者把简历给我，我给你机会，广告只是留给那些希望进入行
业的人的，面经只是一个而且，面到后面真正有经验的就根本不用准备了，已经有不少
人接受我的帮助了，我不需要在解释我的动机.我才刚开始工作，希望能架起一座桥梁
帮助那些需要帮助的别人。
【在 N****n 的大作中提到】
: 你一次说完吧。。。。磨磨唧唧的。。。
: 版上的都是交流学术，面试完友情提供面经经验的。
: 你这个新ID，不说自己的背景，上来就打广告挣钱，还“别把我邮箱挤爆了” 。。。
: 。。。。。。
:
: enabling
: data,
: the
: the
| s*****9
发帖数: 285 | 35 要ISS和ISE的，我是不会，有会的就来吧。。。
Job Description:
Contribute to computer programming efforts for a clinical trial drug project
and to provide programming support for clinical trial data reporting and
regulatory submissions. Assumes protocol level and some project management
responsibility while supporting the Programming and Statistics lead. Able to
support multiple protocols independently and to contribute to integrated
summaries of efficacy and safety. Demonstrates strong SAS programming skills
; participates in protocol team and some project team interactions. Builds
successful relationships and seamless interfaces at the protocol/project
team level. Provides timely and effective communication to the programming
and statistics leads. | s*****9
发帖数: 285 | 36 Job Title: Statistical Programmer II
City/State:Florham Park, NJ
Assignment Duration: 6 months w/ expected renew
One of our clients in Florham Park, NJ is seeking a Statistical Programmer
II to join their team immediately.
6 month assignment
" Provide statistical programming support and validation and help set
specifications of analysis datasets, pooled datasets, statistical tables,
summaries, figures and listing for Phase II-IV clinical trials.
" Employ standardized programs where applicable.
" Provide input into planning documents such as protocol, validation
plan, and report analysis plan. Provide outputs for clinical study reports,
integrated summaries and electronic submissions.
" Help respond to health authority inquiries for submitted dossiers.
" Establish and maintain sound working relationship and effective
communications within biostatistics and statistical reporting and clinical
research.
Education/Experience:
1-2 years of Analytical experience.
BA/BS or equivalent experience in computer science, mathematics, statistics,
life sciences, or related field(s). Intermediate SAS programming skills,
with 2-5 years experience in a medical setting, preferably working with
clinical trial data. Good understanding of clinical trial practices,
procedures and methodologies. Good verbal and written communication skills.
Good interpersonal and organizational skills. Attention to detail and
correctness. Working knowledge of office tools | s*****9
发帖数: 285 | 37 FDA OFFER被我REFER过去的哥们拿到了，先摘下来了，有兴趣加入的朋友下次会给你们
CONFERENCE下，给告诉下他的心得。 | d****z
发帖数: 301 | 38 同志们, 什么叫ICC, 这个就是. slian59: 你敢说不要改假简历么?
请版主把他封了吧 | s*****9
发帖数: 285 | 39 不改简历，改下你做的PROJECTS,丰满一点就可以了，用假名和用假工作经历没必要。 | s*****9
发帖数: 285 | | | | j******n
发帖数: 2206 | 41 gsk 的senior rate是多少？
enabling
data,
the
the
【在 s*****9 的大作中提到】
: GSk的RATE也算比较SENIOR的，ENTRY－LEVEL的RESUME应该比较难上，有SENIOR有兴趣
: 给我RESUME
: Raleigh (Research Triangle Park) position at GSK (Glaxo)
: Clinical Programmer Analyst
: Providing technical support and assistance to clinical study teams, enabling
: them to deliver high quality clinical trial data. This role is centered
: around the extraction, manipulation and reporting of eCRF and non-eCRF data,
: with a close linkage to the development, deployment and maintenance of the
: eCRF data capture package. A working knowledge of GCP and its impact in the
: clinical data acquisition domain is required. A track record of successfully
| s*****9
发帖数: 285 | 42 Available for training now |
|
