h***x
发帖数: 586 | 1 I got from recruiter, please contact her directly if interested,
Christina
c******[email protected]
407-548-0670. | h***x
发帖数: 586 | 2 CALIFORNIA:
0000087272
SAS Programmer (12m)
Bachelor's or Masters in Computer Science or other relevant (Engineering)
degrees with 5+ years of pharmaceutical experience preferred- The work
experience should include at least two years of technical leadership in a
statistical programming environment in a pharmaceutical or biotechnology
environment including the analysis and reporting of clinical trial data-
Knowledge and application of p-values, confidence intervals, linear
regression analysis, advanced general linear models, frequencies, survival
analysis, non-parametric analysis, randomization software, proficiency in
implementing these ideas in clear, efficient SAS code for the purposes of
data analysis and reporting.- Accountable for overall timelines and major
project milestones, as well as overall project quality, integrity and
productivity- Knowledge of base SAS, SAS macro language, graph, FSP, STATS,
SQL as well as other programming languages.- Knowledge of UNIX system,
Oracle Clinical and EDC (electronic data capture) exposure preferred-
Knowledge of clinical systems, medical terminology, clinical trial
methodologies, and software systems development.- Excellent analytical,
problem solving, and computer skills.- Flexible, well organized, excellent
verbal and written communication skills, and interpersonal skills.- Basic
knowledge of FDA/ICH guidelines, the software development life cycle, and 21
CFR Part 11 and other FDA regulations. - Experience working on FDA
submissions. - Able to give effective presentations to small groups such as
Implementation Teams or Statistical Programming meetings
___________________________________________________________
CONNECTICUT:
0000087393 Statistician - 12mo CT Must have a Ph.D. in
statistics with at least 2-3 years experience in clinical trial data
analysis or a MS degree in statistics with at least 4 years experience in
clinical trial data analysis. Provide statistical support including
statistical design and data analysis of clinical trials, and to perform
secondary data analysis to support opt trials & publications. Proficiency in
SAS programming.
0000085850 STAT Programmers Publications CT MS in STAT – They
will be slightly flexible - ie BS candidate with 5 yrs but at the same rate
? 3 yrs experience? Writes great in English? Speaks excellent English
0000087300 Clinical Programmer - 12m CT BS with 7-9 years
experience. 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.
__________________________________________________________
ILLINOIS:
0000086620 (35009)Statistician/SAS R (6M) IL (35009) Statistician
(SAS R experience) (1 Opening, 6+ Months Contract)Overview:Company needs
someone with strong computing skills (strong in R and preferably also in SAS
, plus solid experience in Unix, JAVA, HTML, Perl, etc.), along with strong
statistical training, and formal masters or Ph.D. degree in statistics.
Formal Job Description: - Statistician in the Exploratory Statistics team in
site. - Educational Qualifications: Masters or Ph.D. in statistics, with
coursework/experience in biochemistry Primary Function: - Provide
statistical consulting and computing support for projects in areas such as
drug discovery and pre-clinical and biomarker research (genomics, imaging,
etc.), animal studies, in-vitro screening, clinical assays, etc.
Qualifications: - At least two, but preferably five years of related
experience with demonstrated skills/accomplishments as a statistician. -
Applications are also welcome from recent Ph.D. graduates that have done
research on some of the topics noted above, with training and practical
experience during school work. - Expertise in statistical methodologies such
as nonlinear regression, mixed effects models, multivariate analysis,
predictive modeling, machine learning methods, etc., required. - Strong
school work (e.g., dissertation topic) and/or relevant academic/industry
experience on topics related to drug discovery, genomics and other
applications mentioned above. - Strong computing skills in R is REQUIRED. -
Familiarity in web-based tool development, JAVA, Perl, Visual Basic, etc.
and background in bioinformatics, biochemistry, and related subjects are
also preferred.- Also, please note that excellent verbal and written
communication skills are required.
0000086495 (34664) Clinical Stat II IL Master's degree in
Statistics is REQUIRED, excellent SAS programmer, 1 to 3 years industrial
experience in the related area.
0000085329 (32583) SAS Program (6M) IL Depending on
qualifications position maybe offsite. Looking for the best fit for the
position.Generate tables, listings, and graphs for compound projects.
Responsible for the validation and quality assurance of any output produced.
Generate and review validated table, listings, and graph output meeting the
needs of Clinical Projects. Prefer candidate with clinical experience. SAS
program experience required.Depending on qualifications position maybe
offsite. Looking for the best fit for the position.
0000085328 (32593) SAS Program (6M) IL VERY IMPORTANT! The
preferred candidate will have SAS programming experience in the
pharmaceutical industry and SAS programming experience is required.Generate
tables, listings, and graphs for compound projects. Responsible for the
validation and quality assurance of any output produced. Generate and review
validated table, listings, and graph output meeting the needs of Clinical
Projects. Prefer candidate with clinical experience. SAS program experience
required.
__________________________________________________________
MASSACHUSETTS:
0000086253 Biostatistician (12M) MA .MS or PhD in Statistical
related discipline, with preferences towards Biostatistics, 2-5 years’
pharma with exp in SAS, statistical analysis, scientific graphing and data
manipulation, some knowledge of NDA’s/BLA’s/IND’s & eCTD submissions.
Position could convert to perm for the right person.Position is providing
statistical support for Phase I/II and Health Economics / Outcomes Research
focusing mainly on analysis planning, developing specs for derived datasets,
TFL shell developments, ad hoc data analysis, QC and communication with
other functions.
0000086255 Biostatistician (12M) MA • Ph.D. in
Biostatistics or Statistics• Must have extensive knowledge in assay
development and validation & familiar with biology jargons.• Knowledge
and experiences in multivariate analysis, survival analysis, data mining,
GLM, mixed effect model. • Solid understanding of DoE • Work
effectively in a cross-functional team • Willing to learn biology and
a team player • Strong computational skills in R, S-plus and SAS•
; Excellent consultation skills Position is assisting sr. biostatisticians
in conducting design and analysis of studies in clinical biomarkers, in
vitro assays, in vivo assays and providing statistical consultation.
0000086257 Biostatistician (12M) MA Ph.D. in Biostatistics or
Statistics• Knowledge and experiences in multivariate analysis,
survival analysis, data mining, GLM, mixed effect model. • Solid
understanding of DoE • Excellent consultation skills • Good
communication and interpersonal skills • Work effectively in a cross-
functional team • Work effectively under pressure and timeline •
Creative thinker with the ability to execute • Willing to learn
biology and a team player • Strong computational skills in R, S-plus
and SAS.
0000086976 (2954) Stat Prog Analyst (1Yr) MA (2954) Statistical
Programming, Senior Analyst III (1 Opening, 12+ Months contract)Overview:&#
8226;Serves as lead Statistical Programmer to achieve milestones on one or
more studies. •Develops and implements Statistical Programming
Specifications and QC plans with lead statistician for one or more studies.
•Works closely with study team to assure quality data and deliverables
. •Provides resource estimates, timelines, and expectations to other
team members. •Ensures standards at a drug program level; integrates
data across multiple studies or drug programs. •Is accountable for
identifying issues and the development and implementation of solutions to
problems. •Is responsible for mentoring other programmers.
Requirements: •Viewed as expert in the field of statistical
programming. •Able to handle a moderate to large volume of complex
tasks with some supervision. •Able to manage statistical programming
work in one drug program. •Able to handle ad-hoc requests from other
departments with minimal guidance. •5 - 7 years SAS Base programming
with 5+ years using SAS STAT, GRAPH and MACRO •5 - 7 years relevant
industry experience •Extensive knowledge of drug development process
and clinical trials •Extensive knowledge of drug submission
requirements, relevant ICH and FDA/EMEA guidelines, CDISC standards
Education •Bachelor’s degree or equivalent, preferably in a
scientific discipline such as Statistics, Mathematics, Economics, Computer
Science, IT, Biology, Social Science, etc
0000087349 Sr. Statistical Programmer 6mo MA - Bachelor's degreee
in Biostatistics, Statistics, Computer Science, or a related field - 5
years of SAS and relevant pharmaceutical industry experience
0000086672 Statistical Subs Mgmt (6+Mo) MA (2916) Sr. Analyst
III – Statistical Submissions Management (2 Opening, 6+ Month Contract)
Required Education/Experience:- Bachelor’s degree or equivalent, preferably
in a scientific discipline (i.e. Statistics, Mathematics, Economics,
Computer Science, IT, Biology, Social Science, etc.) -Great general computer
proficiency, including Microsoft Suite applications -3-7 years Adobe
Acrobat and electronic submission applications experience utilized for
electronic submission purposes -3-7 years SAS experience with some
demonstrated programming language experience -CDISC standards experience -3-
7 years relevant experience in the pharmaceutical, biotechnology industry or
CRO
0000086910 Sr. Statistical Programmer - 6 MA Minimum
Qualifications Minimum Qualifications:- Bachelor's degreee in Biostatistics,
Statistics, Computer Science, or a related field - 5 years of SAS and
relevant pharmaceutical industry experience
________________________________________________________________
MARYLAND:
0000085450 Oracle Dvp/Java (6M to PERM) MD * 3+ years of PL/SQL
database design/development (MANDATORY), software engineering or related
experience• Experience using PL/SQL for implementing data-intensive
and complex business logic, • Experience creating & maintaining korn
shell & SQL scripts,• Experience with Oracle Reports, Java, JavaScript
, ExtJS and Linux/UNIX is desirable,• Strong knowledge of software
development life cycle,• Knowledge of RMAN for both backup and
recovery,• Clinical trial experience a plus.NOTES: Contract to perm
after 6 mos.
0000086316 Statistician-6M (Con to Perm) MD Candidates should
have M.S. in statistics, biostatistics or related field and 1-3 years of SAS
experience. A working knowledge of the UNIX/Windows environment,
familiarity with SAS procedures for statistics, graphics, SQL, and macro
languages and other analysis/graphics packages would be helpful. Experience
in medical research with several years serving as a Study Manager is
desirable. Individual should be ambitious and versatile with skills in
preparing oral and written presentations
0000087360 Clinical Programmer II - 6 mo MD Clinical Programmer
II -5+ years SAS programming Hiring mgr is- j*********[email protected] month
contract with option to extend-location Rockville,MD JOB SUMMARY Responsible
for providing SAS programming activities in Clinical Programming (CP). Be
able to write, implement and validate programs that perform any task, as
assigned. Responsible for quality control of own work and the work of others
as assigned. Demonstrates increasing ability to be innovative and
productive in clinical trials data. Provides guidance to less experienced
programmers as needed.JOB DUTIES & RESPONSIBILITIES• Creation/
retrieval/uploading of clinical data to/from/between Clinical Data
Management Systems (CDMS) and other systems (IWRs, Labs, etc.).•
Programs, documents, and validates edit checks as specified in the Data
Validation Plan for a given protocol, or in response to ad-hoc requests.&#
8226; Creates output and/or make data in the form of HTML, RTF, and/or PDF
files accessible to authorized staff, as appropriate.• Works under
direct supervision of a more experienced SAS programmer.• Helps write,
revise, and maintain departmental Working Practices, Guidelines, and SOPs.&
#8226; Provides technical assistance, according to ability, to others in the
HGS SAS user community.• Attends appropriate project team meetings as
a representative of CP.• Actively solicits ideas from our own and
other departments that would lead to the creation of programs to meet those
needs.• Helps define and create programming standards in a production
data processing environment.• Performs other functions as necessary or
as assigned.COMMUNICATION• Keeps manager(s) informed of progress and
any issues.• Tracks progress and issues using proven tools and metrics
.• Communicates easily whether verbally or in writing.•
Expresses ideas concisely and clearly. • Listens attentively to
suggestions or concerns.• Determines when and how to escalate issues.&
#8226; Develops and maintains effective and effic
0000087002 Sr. SAS Programmer - perm MD Requirements/
Qualifications:Proven success in the development, documentation and
qualification of programs to generate Tables, Listings and Figures for
Clinical Studies, and in support of data cleaning activities. Demonstrated
experience in base SAS, SAS MACRO, SQL, Graph (or equivalent) and using ODS
for presentations and data mining reports. Education: Bachelors/Masters
degree in Computer Sciences, Statistics, Mathematics or relevant scientific
discipline. Experience: Bachelors degree and 5 to 8 years experience, or
Masters degree and 2 to 5 years experience in SAS Programming. 4 years
experience in drug development. Demonstrated knowledge and understanding of
programming standards and methodologies, GCP, ICH and related FDA
regulations. Experience with the design and implementation of CDISC standard
is required. A background in statistics, or having proven experience to
assist in design of study analysis is a plus. Experience with Oracle
Clinical/RDC, Integrated Review, or other relational data management
software is considered a plus.
0000086391 Sr. SAS Validation Progr. 12mo MD BS with 5 years of
SAS Programming skill applied in pharmaceutical industry or a MS with 3
years applicable work experience using SAS aplied in the pharmaceutical
industry.Full Time allocation and Onsite Rockville Daily; 12 Month contract
with potential to extend.Must be extremely proficient in SAS Programming
validation of Analysis data sets , SDTMs, Tables and Listings.Must have
working experience with CDISC / SDTM / AdAM standards.More than FIVE YEARS
IN PHARMA INDUSTRY required. Very strong communication skills needed.
Reliability is essential.
______________________________________________________________
MISSOURI:
0000087061 Biostatistician (6M) Temp/Perm MO Biostatistician (1
Opening, 6 Month Temp-to-Perm Contract):Education/Experience:- MS (PhD
preferred) in Biostatistics/Statistics with industry experience. - Oncology
background could be helpful for future projects, but is not required.-
Experience in analgesia trials preferred. - Five years full-time experience
in the design, analysis, and reporting of clinical trials for regulatory
submissions. - Participation as statistical lead in meetings with regulatory
authorities. Preferred: - Presentation skills and comfort with
presentations to non-statistical audiences. - High degree of knowledge about
and proficiency in SAS programming
________________________________________________________________
NORTH CAROLINA:
0000085237 SAS Analyst 12 Mo NC Two years of experience with
large national/international cross-sectional and longitudinal healthcare
databases, statistical programming, and database management to conduct
Epidemiology/Health Outcomes studies preferred. Masters degree in Statistics
, Epidemiology, Health Outcomes or SAS Certification preferred.
0000087190 Business Systems Analyst NC Basic qualifications
applicable experience• Experience in pharmaceutical industry or health
-related field • Proven experience of applying customer service and
technical skills• Proven ability to work effectively within
interdisciplinary teams• Solid technical background and computer
proficiency in a variety of databases and software applications; technical
aptitude• Solid knowledge of clinical development processes and
procedures, including related functional areas and regulations as required&#
8226; Ability to work on complex or multiple project assignments•
Demonstrated ability to manage tasks with limited supervision•
Exhibits enhanced customer service orientation and excellent interpersonal
skills with ability to communicate professionally Preferred qualifications:
• Experience in one or more of the following technologies is
preferable:o Microsoft Project or similar planning softwareo IntraLinkso
Cognos Reporting toolso Microsoft SharePointo SQL o Oracle (database
programming / query skills)• Software development experience in a
regulated pharmaceutical environment• 1st and/or 2nd level system
support experience • Track record of providing high quality customer
support
__________________________________________________________
NEW JERSEY:
0000086751 Program Manager (6M) NJ 5 – 10 years experience
working in the Pharmaceutical Industry preferably managing a large IT
project for Regulatory Affairs as well as demonstrated experience of
successfully managing a large and complex implementation project in a
multifaceted and multinational setting. Knowledge of Regulatory Affairs
operations and systems is desirable, including knowledge of document
management systems, labeling systems, submission management and submission
publishing systems. Experience in managing the development and implemention
of a “hosted” solution is a major plus. Bachelor’s degree preferred as
well as PMP or similar related professional certification. Must be able to
organize and prioritize work, and function independently. Excellent
communication, problem solving, time-management, and decision-making skills
along with attention to detail is a must.
0000086926 Study Designer/Builder (12m) NJ 2+ years' pharma exp
with technical expertise in Clinical systems with 5+ years' database build/
analysis experience. Must have Inform experience. DsNavigator & I-Review.
Extensive experience in EDC, eCRF, relational databases, PL/SQL, SQL and SAS
programming concepts and logics.
0000086686 SAS Developer-Lead 12mo NJ Required:Excellent skills in
the SAS programming language, especially in the SAS data step and
SQLExperience with SAS/AF and SAS ODSVery strong attention to quality and
detailExcellent interpersonal and communication skillsMasters or bachelors
degree in computer science, engineering, a physical science, mathematics, or
statisticsAt least three years of programming experienceAbility to learn,
and interest in using, Spotfire and Pharsight PKSDesired but not required:
Experience with Watson LIMS and Oracle ClinicalPreparation of data for use
by NONMEMPharmacokinetic experienceUse of Thermo’s EP2 and Kinetica
softwareFamiliarity with principles of quality control and the validation of
computer programsBasic UNIX understandingPharmaceutical industry
experiencePharsight PKS experienceSpotfire experienceExperience in
programming to meet SDTM requirements
0000083105 Project Manager NJ Education:MPH/MBA/Ph.D. degree in a
relevant area, with a record of strong academic and business achievement
Experience:* Prior experience in pharmaceutical management consulting or
other pharmaceutical business analysis field, solid understanding of
healthcare industry and markets* Broad understanding of pharmaceutical
prescription data* Exceptional capacity for quantitative and qualitative
analysis, with strong quantitative research analytical skills and experience
* Experience with statistical and survey analyses a plus* Superior problem
solving skills; ability to think clearly about business issues and define
and evaluate alternative solutions, desire to engage in strategic thinking *
Effective task management, oral (including presentation) and written
communication skills; ability to work with senior leaders and other cross-
functional groups to build consensus* Ability to learn quickly and adapt to
rapidly changing roles and responsibilities* Advanced skills with Microsoft
Excel and Microsoft PowerPoint
0000086917 Biostatistician (6m) NJ •University degree (
MSc, PhD) in Statistics, Mathematical Statistics or Biostatistics, or
equivalent experience.•Comprehensive knowledge of Clinical Drug
Development processes and ability to and ensure compliance with regulatory
authorities, quality and technical standards. •3+ years of statistical
experience with Global pharmaceutical companies, Clinical Research
Organisations, or Business Process Outsourcing companies. •Computer
programming aptitude•Good knowledge of spoken and written English.&#
8226;Good communication and presentation skills•Demonstrated ability
to work collaboratively in a team environment as well as independently.&#
8226;Demonstrated ability to manage own priorities and goals.
0000087268 Sr. Statistician (12M) NJ • Completed Ph.D. in
Statistics with 8+ years pharmaceutical R&D experience or M.A. with 10+ year
pharmaceutical R&D experience with a focus on statistical methods
appropriate for clinical trials and secondary analyses required.•
Excellent written and oral communication skills are mandatory.•
Interpersonal communication and organizational skills.• Experience in
oncology is a decided advantage.• Demonstrated skill in the planning,
analysis and reporting of clinical trials. • Detailed knowledge of
statistical methodologies and statistical regulatory requirements. •
Previous experience in leading and completing a task force and/or
supervising statisticians.• Up-to-date knowledge of clinical trial
design concepts.• In-depth knowledge of all phases of the drug
development process.• Demonstrated ability to work in a team
environment with clinical team members.• Up-to-date knowledge of
statistical development methodologies and optimal methodologies acceptable
to regulatory agencies.• Up-to-date knowledge of relevant project area
's clinical trial development and regulatory requirements.
0000087151 (89249) Statistician (12M) NJ Statistician
Position requiring significant independent SAS programming: MS/PhD degree in
statistics/biostatistics, with at least four years of experience working
with/analyzing all Phases of clinical trial data. Must have experience with
Health Authority submissions (FDA and other countries). Pharmaceutical or
CRO experience required. Experience working with bleeding /clotting analysis
. - good knowledge of clinical study designs, common analysis methods,
descriptive and inferential statistics, summarization of data and
presentation practices - hands on experience of statistical analysis -
proficiency in SAS, experience with SAS macros - preferred experience in NDA
/BLA submissions - good knowledge of CDISC SDTM and ADaM - ability to work
independently, toward the primary responsibility of preparing and validating
analyses and preparing supporting documentation - good oral and written
communication skills - able to prepare specification documents; verify
against programming and bring issues to the team.
0000087263 Sr. Statistician (12M) NJ PhD in Statistics or MS in
Statistics with solid pharmaceutical experience5+ years of Pharmaceutical
experienceStrong SAS Programming ExperienceValidation ExperienceData
Integration experience
0000087081 Biostatistician - 12 mo NJ Masters with 5-7 years of
experience. Provide statistical support including statistical design and
data analysis of clinical trials, and to perform secondary data analysis to
support opt trials & publications. Proficiency in SAS programming.
0000087376 Statistician - 6mo NJ Must have strong experience
in preparing or supporting the integrated summaries of safety and
effectiveness (ISS/ISE) for a submission. we do not need a top-level stat to
design the ISS/ISE; we would need someone in a supporting role.
0000086444 Sr. Clinical Data Analyst (SAS NJ • 5-7 years’
SAS clinical trial programming with strong exp developing SAS Macros and
experience in CDISC SDTM. Position will support CDM in Oncology – working
on data edit checks, data cleaning activities, data review & complex
listings. Experience in review of CRF’s, eCRF’s, SAS/Base, SAS/Graph, SAS
Macro, SAS/AF/SQL. Exp handling external data (i.e, lab data), exp using J-
Review/I-Review. Exp in MedDRA & WHODRUG, as well as relational databases (i
.e., Oracle) and software dev life cycle. Understanding of SAS-based
application development. Understanding of EDC (Inform) is a plus.
0000087208 SAS Programmer/DCF Supp 6m NJ SAS Programmer/DCF
Supp 6m-SAS Programming skills.Good communication and writing skills are
mustBA/BS or advanced degree. BS in relevant in the programming areas would
be preferred
0000086931 Sr. SAS Programmer NJ 5-8 years of SAS Programming
experienceSr. SAS Programmer needed for a one year, renewable position.BS
Degree in related fieldMinimum 5 years of SAS programming experience in the
pharmaceutical industryExperience with ISS/ISE as well as ADaM “desired”
not required. Must have solid experience of coding analysis datasets and
tables, listings, graphs programs from scratch.Good documentation skills are
desired.
0000086911 SAS Programmer NJ Minimum Requirements:•
University degree (Mathematical, Statistical, Computer Science or Life
Science) or equivalent experience•Comprehensive knowledge of Clinical
Drug Development processes and ability to and ensure compliance with
regulatory authorities, quality and technical standards. •3+ years
relevant programming experience•Computer programming aptitude•
Good knowledge of spoken and written English•Good communication and
presentation skills•Demonstrated ability to work collaboratively in a
team environment as well as independently•Demonstrated ability to
manage own priorities and goals•Demonstrated ability to work
collaboratively in a team environment as well as independently•
Demonstrated ability to manage own priorities and goals
0000086667 Technical Team Leader SAS Prog NJ 10 years of SAS
programming experience in pharmaceutical industry with 2 years of experience
in a technical or managerial leadership position.Experience with ISS/ISE
programmingHands-on experience writing and validating SAS programs for
analysis datasets and TLFs and preparing Define.pdf documentStrong
analytical, coordination, documentation and communication skillsAbility to
multitask and prioritize studies.
0000086445 Sr.Clin Data Analyst (SAS Lead NJ • 5-7 years’
SAS clinical trial programming exp with extensive SDTM knowledge for mapping
and related programming, exp in CDM Dept. Must be strong in SAS Macro. Must
have project lead experience (please specify). Oncology exp a plus.
Position is reviewing CRF’s/eCRF’s, edit check specification, writing
complex macros, reports, experience with SAS applications & systems.
Experienced in SAS/Base, SAS/Macro, SAS/Graph, SAS/AF/SQL, experience
handling external data (i.e., lab data), PK and of using I-Review / J-Review
. Good understanding of CDISC, SDTM, MedDRA & WHODRUG. Understanding of EDC
(Inform) and relational database (i.e., Oracle) a plus.
0000087269 SAS Programmer (12-18m) NJ SAS Programmer (12-18m)-
Priorities:-Data management experience -expertise in SDTM mapping - prior
experience data handlingMA/MS/MBA Or equivalent computer science,
mathematics, statistics6-8 yrs of related experienceGood working knowledge
of SAS, S-Plus, R software (JMP beneficial).Knowledge/experience in clinical
database design or data managementMinimum of 3 years experience in
programming support for clinical trial managementKnowledge of global
clinical trial Practices, procedures, methodologies. (replace with
regulations, guidances and compliant practices)Good organisational skills,
plus an understanding of resource & budgetingGood interpersonal and
communication skills and the ability to operate effectively in a global
working environment Work calmly under pressure and meet
deadlinesProfessional, positive and enthusiastic attitudeA good
investigative and meticulous approach to all activities and tasksTransparent
approach, clear and preciseTeam playerAssist improving the effectiveness of
the organisation such as developing new processes, and systemsWork
effectively and efficiently with internal partners
0000087380 (89129) SAS Programmer (12M) NJ Qualifications: The
incumbent must have an MS degree in a biological science, Statistics,
Computer Science or a related field and at least 6 years related experience
of which 5 years within the pharmaceutical industry and 4 years experience
as a SAS programmer. Or a BS degree with 8 years related experience of which
5 years within the pharmaceutical industry and 4 years experience as a SAS
programmer. A strong understanding of Clinical Data Management processes.
Strong experience in SAS programming and ODS. Strong knowledge of database
structure design, especially the CDISC SDTM data model. Strong understanding
of clinical study designs. Very good understanding of data handling
processes and preferably clinical study programming. Experience in designing
and implementing data management process tools is a plus. Good
understanding of the drug development process, including all Phases I-IV.
Good understanding of regulations, standards and guidelines (e.g. ICH, GxP,
CDISC, European Clinical Trials Directive, Privacy rules [HIPPA]).
Familiarity with validation of systems Ability to lead projects Ability to
work independently as well as part of a team environment. Ability to
communicate outside of the programming group. Effective self-management and
organizational skills. High commitment to quality and attention to detail.
Excellent negotiation and issue management skills. Fluency in English.
Excellent written and oral communication skills.
0000087343 SAS Programmer (12M) NJ • Knowledge of FDA
regulations (21 CFR part 11) and guidelines in new drug development and
application process required.• Candidate must have worked in a Unix
environment and have basic knowledge of Unix commands.• The person
will be joining an established team responsible for creating an analysis
data set based on a clinical database.• The person will be responsible
for developing tables, graphs and listings and will, in turn, provide
statisticians the information. The statisticians will generate reports for
the FDA that will play a pivotal role in the reviewing of new drug
applications.• Candidate must have a background in both statistical
analysis and clinical trials.• Must have a degree is statistics
0000086969 Statistical Programmer III 6m NJ Statistical
Programmer III 6m-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. SAS. BA/BS
0000085985 Clinical Programmer - 12mo NJ Masters in
Statistics required with 7 years exp with at least 2 years in Pharma/CRO
setting (not university). Preferably someone that has been at one place for
at least 1 ½ -2 years. 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.
0000085989 SAS Programmer - 6mo NJ • Experience in SAS
Programming and Biostatistical analyses for clinical trials in the
pharmaceutical or biotechnology industry. At least 4 years of programming
experience in a CRO, Pharma, or biotech company, of which at least two years
in oncology (solid tumor studies). Experience in supporting ISS/ISE and NDA
submission a major plus. • Bachelor degree or higher in mathematics,
statistics, computer science, physics or related quantitative field
preferred.• Familiar with CDISC conventions, i.e., SDTM and ADaM
models and hands on experience implementing these models.• Attention
to detail. Analytical and logical approaches to tasks. Expertise in the
production and reviewing of datasets, analyses, tabulations, graphics and
listings from clinical trial data• Strong DATA step programming skills
. Experience with ODS, Base SAS, SAS/STAT, SAS/GRAPH, PROC REPORT, SAS Macro
language. Experience working with EDC data sets.• Solid understanding
of clinical trial data and extremely hands on in data manipulations,
analysis and reporting of analysis results.• Good organizational and
communication skills, the ability to work in a collaborative environment
0000087308 Statistical Programmer II (6m) NJ Statistical
Programmer II (6m)-Experience using SAS in the analysis and the reporting of
pharmaceutical dataWorking knowledge of database design/structures
Expertise with SAS (including SAS macro language) Experience in Oncology
therapeutic areaMasters degree preferred
0000086769 Epidemiology Prog. Coord. 2 yr PA Qualifications:
Master's degree preferred in epidemiology (or closely related discipline,
such as biostatistics, biometry, public health or biological sciences) or
Bachelor's degree plus three years related job experience, or equivalent
experience. Exposure to statistics and basic sciences and or/medical
research. Must have strong communication and organization skills. Academic
or practical experience in experimental design. Responsibilities: Under
general supervision of manager of director. Coordinates in all aspects of
epidemiologic research studies, including preparation of the study protocol
and design of studies, ordering and shipping of all equipment and supplies,
design and preparation of date collection forms, tabulating data and
preparing data summaries for regulatory submissions, publications and
technical reports.
______________________________________________________________
PENNSYLVANIA:
0000085574 Medidata Rave Proj. Spec.10m PA has started 3 new
Rave studies simultaneously and although severalstaff members have received
training, they do not have practical use withthe system. An experienced edit
check programmer will help ensure success.Fully trained and proficient on
the use of Rave e data capture (v5.6.4)1-2 years of Rave edit check
programming and custom function programming1-2 years of J Review / I Review
reports programmingPrograms edit checks and custom functions in Rave.
Program clinical data Reports using tools like J-ReviewAssist with database
set-up programming for clinical trialsAssist with batch uploading of
external data. Clinical views and transfer data out of the Rave database.
0000086628 (19577) Jr. Clin Stat (3M) PA The ideal candidate
will have either a BS or MS in Math or Statistics. In addition the candidate
should be able to program well in at least one common programming language
(e.g., SAS or R or MatLab) and be willing to learn R.
0000087014 Sr. Stat Programmer (6m) PA Education &
Experience Requirements:• Bachelor’s degree in a scientific field
required, Master of Science degree preferred • At least 9 years of
statistical programming experience using SAS in the pharmaceutical, contract
research organization, or other clinical research setting Key Skills and
Competencies:• Must have experience leading efforts to create
integrated analyses datasets for safety reporting • Must have
experience in programming project team management • Must have
experience integrating data sets from archived and current studies •
Must have experience managing programming activities and collaborating with
other functions • Experience in developing project plans including
time and resource estimates • Experience in development and
implementation of statistical programming standards is preferred •
Knowledge of software systems development is a plus • Experience using
industry standards for data set design as defined by Clinical Data
Interchange Standards Consortium (CDISC) • Knowledge of appropriate
FDA and other regulatory (i.e., ICH) guidances • Excellent working
knowledge of Base SAS, SAS/STAT, SAS Macro language and SAS SQL; SAS/GRAPH a
plus. Experience using SAS version 8.2, 9.1.3 or 9.2 • Proficient in
developing own code as well as modifying existing code • Experience
producing detailed and accurate documentation for statistical programs &#
8226; Excellent analytical, problem solving and organization skills with the
ability to work on multiple tasks • Flexible to changing priorities,
detail-oriented, works well under pressure with initiative to take on
unfamiliar tasks • Excellent communication skills (verbal and written)
as well as good interpersonal skills • Strong organizational skills
and the ability to work in a collaborative environment, and desire to
improve skills are essential • Experience working with CROs and other
Service Providers
0000087314 Biostatistician - 6mo PA BS with 3 years experience?
Manage Biometrics project teams and track department project activities (
including project revenue) and provide status updates.? Represent department
on interdepartmental project teams.? Serve as contact with clients for
statistical aspects of clinical studies.? May serve as project leader for “
back-end” projects involving single studies.
0000086457 Statistician WA MS Statistics/Biostatistics with at
least 2 year of related experience Broad experience in clinical statistics,
excellent written and oral communication skills. Strong ability to handle
multiple projects simultaneously. Oncology experience is preferred.
0000083201 Senior Statistical Programmer Qualifications:&#
8226; B.S. degree required, M.S. degree preferred.• Experience leading
SAS programming projects in the pharmaceutical industry demonstrated by the
ability to independently act as the point of contact on the statistical
programming for all phases of clinical trials, directing the work of one or
more programmers.• Proficient in industry standards, medical
terminology, and clinical trial methodologies.• Posses project
management skills within the Statistical Programming function.•
Evidence of the competencies as described in the next section. | h***x
发帖数: 586 | 3 12M - 12 month contract.
The Illinois positions are the most flexible with experience, if your have
some research/Clinical trial experience even in academia they will consider
you. | p*******r
发帖数: 1951 | 4 多谢！去撞撞运气。
consider
【在 h***x 的大作中提到】
: 12M - 12 month contract.
: The Illinois positions are the most flexible with experience, if your have
: some research/Clinical trial experience even in academia they will consider
: you.
| h******n
发帖数: 190 | | h******s
发帖数: 3420 | 6 干的好，转正
干的不好，去死
干的不好不坏，接着当合同工
【在 h******n 的大作中提到】
: 这些都是合同工啊，一年后怎么办？
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