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<title>craigslist | science/biotech jobs in northwest suburbs</title>
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<description></description>
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<dc:title>craigslist | science/biotech jobs in northwest suburbs</dc:title>
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<syn:updateBase>2009-12-26T14:35:13-08:00</syn:updateBase>
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<item rdf:about="http://chicago.craigslist.org/nwc/sci/1519879150.html">
<title><![CDATA[Manager Clinical Budget Analysis- Abbott Planning and Resource Group (Lake County, IL)]]></title>
<link>http://chicago.craigslist.org/nwc/sci/1519879150.html</link>
<description><![CDATA[<p><font size="2"><font face="Arial" color="#0062e1" size="2"><font face="Arial" color="#0062e1" size="2"><font face="Arial" color="#0062e1" size="2">

<p>At Abbott, we provide the perspectives and experience necessary to translate science into real solutions for patients in over 130 markets worldwide. Today, 72,000 Abbott employees are doing work that matters.</p>

</font></font></font></font></p>

<p>PRIMARY FUNCTION / PRIMARY GOALS / OBJECTIVES:
Performs financial analyses and budgetary reconciliation of the clinical trial budgets for one or more Therapeutic Areas. Utilizes multiple financial and reporting systems including: contract database, budget database, payment tracking databases, and investigator budget determining software. Collects, summarizes, consolidates and verifies data from multiple sources for confirmation of budget source, variance from planned budget and resources, monthly budget tracking, reporting and reconciliation as well as regular aggregate review. Facilitates interpretation and understanding of data. Identifies issues, cost savings and adjustments and communicates to clinical study management scenarios for addressing them. Interfaces with Clinical Field Operations study management teams and Finance, Clinical Project Teams, CPRM, Abbott Affiliates, Clinical Research Organizations, and other functional areas to ensure full accountability of clinical study budgets and resource utilization.

<p>ACCOUNTABILITY / SCOPE:<br>
Responsible for managing assigned therapeutic area study budgets simultaneously. Accountable for meeting project objectives on schedule and within budget. Responsible for development and oversight of investigator grant budget process to ensure fair market value. Reviews key decisions impacting budget/timelines with senior CPRM Management, Finance, and GPT/study teams. Provides recommendations for resolution of budget variance issues. May manage other junior department members and oversee clinical analysis activities.</p>

<p>Basic Qualification:<br>
- 	Minimum of 8 years combined experience in clinical research operations and/or financial analysis required.<br>
- 	Familiarity with basic finance and accounting processes and techniques, as well as budgeting, contracting, and payment processes and systems for clinical studies.<br>
- 	Expertise in clinical study costing, Investigator Grant budgeting systems, MS Office applications, including Excel, Word and PowerPoint required.<br>
- 	Requires 1 to 2 years experience either supervising or managing people with demonstrated leadership skills.<br>
- 	Candidates should be flexible, able to work with minimal supervision and have good analytical, organizational and team skills.</p>

<p>Preferred Qualifications:
- 	Prefer Pharmaceutical or CRO experience. Requires ability to understand scientific, financial, business facts and metrics.</p>

<p><font face="Arial" color="#0062e1" size="2"><font face="Arial" color="#0062e1" size="2"><font face="Arial" color="#0062e1" size="2">

<p>Through numerous local, national and international accolades, Abbott is regarded as an employer of choice for our commitment to workplace excellence. Our employees are given the tools to succeed, lead and grow, with challenging opportunities and work that makes a difference. Through our diverse healthcare businesses, we connect people and potential in ways that no other company can. </p>

<p>Discover a world of opportunities at Abbott. </p>

<p>&nbsp;<strong><em>EEO Statement: </em></strong>

<p>At Abbott, we believe that diversity drives innovation. Innovative thinkers who are passionate about the work they do, Abbott employees are representative of the diversity of the patients we strive to serve every single day across the globe.</p></p>

</font></font></font><font face="Helv" size="2"><font face="Helv" size="2"><br>
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<br>
<br>
If interested, please apply online at <a href="http://track.jobviper.com/ViewJob.asp?id=654734-1660-5244"  rel="nofollow">http://track.jobviper.com/ViewJob.asp?id=654734-1660-5244</a>
]]></description>
<dc:date>2009-12-21T12:42:01-06:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://chicago.craigslist.org/nwc/sci/1519879150.html</dc:source>
<dc:title><![CDATA[Manager Clinical Budget Analysis- Abbott Planning and Resource Group (Lake County, IL)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-12-21T12:42:01-06:00</dcterms:issued>
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<item rdf:about="http://chicago.craigslist.org/nwc/sci/1511158317.html">
<title><![CDATA[Sr. Manager, Pharmacoepidemiology &amp; Epidemiology (Deerfield Park, Illinois)]]></title>
<link>http://chicago.craigslist.org/nwc/sci/1511158317.html</link>
<description><![CDATA[The Sr. Manager provides consultation for and facilitating the systematic planning, collection, and synthesis of global pharmacoepidemiology information for all Takeda products in collaboration with among others Pharmacovigilance, Clinical Sciences, Regulatory Affairs, Medical Affairs etc. The following are key elements of the position's objectives:<br>
•	The incumbent provides global strategies and pharmacoepidemiology research plans to further the commercial and clinical objectives for the therapeutic area or product<br>
•	The incumbent directs globally the designs and conduct of qualitative and quantitative analyses of pharmacoepidemiology studies (cohort studies, case-control studies etc.) to generate data that are important for decision-making in each stage of a product's lifecycle<br>
 <br>
ACCOUNTABILITES:<br>
•	Direct comprehensive pharmacoepidemiology strategies to help achieve product strategic targets and objectives (includes Clinical, Pharmacovigilance, Regulatory and Commercial).<br>
•	Oversee natural history of disease studies to understand the inherent risks associated with the indications for which medications are approved or under development<br>
•	Translate the vision of pharmacoepidemiology in cross-functional objectives and activities<br>
•	Manage the use of longitudinal databases, SRS databases and literature<br>
1) to develop an understanding of potential safety issues for new compounds and new indications, based on experience with related compounds, and  <br>
2) to contribute to position papers relative to marketed products<br>
•	Effective communication of pharmacoepidemiology plans and deliverables in U.S. and globally, both to internal and external audiences.<br>
•	Present pharmacoepidemiology data and evidence to regulatory agencies and advisors/opinion leaders and convey logic<br>
•	Partner with Clinical Sciences and Pharmacovigilance in clinical trial planning, creation and conduct of risk management strategies utilizing pharmacoepidemiology research techniques.<br>
•	Provide pharmacoepidemiology expertise during due diligence and make recommendation based on the findings<br>
•	Represent, Takeda at pharmacoepidemiology meetings, and relevant Regulatory Agency meetings<br>
•	Be an advocate for pharmacoepidemiology activities<br>
•	Set goals, supervise, and evaluate performance of staff as well as planning growth of personnel.<br>
Qualifications<br>
EDUCATION, EXPERIENCE AND SKILLS:<br>
Education:<br>
•	Required: Masters in Pharmacoepidemiology, or Epidemiology, with minimum 8 years experience in the pharmaceutical industry, CRO health-related consulting company, or academia (or a combination of afore-mentioned)<br>
•	Preferred: PhD in Pharmacoepidemiology, Epidemiology, or MD with a Masters in Pharmacoepidemiology or Epidemiology, or PharmD with a Masters in Pharmacoepidemiology or Epidemiology with minimum 5 years experience in Pharmacoepidemiology, or Epidemiology, in the pharmaceutical industry, CRO health-related consulting company, or academia (or a combination of afore-mentioned).<br>
Experience:<br>
•	Experience with risk management planning is desired.<br>
•	Ability to follow scientific arguments, identify pharmacoepidemiology scientific data needs<br>
•	Extensive experience with observational database analyses and methodologies<br>
•	Ability to obtain pharmacoepidemiology regulatory opinions, assimilate data effectively define an epidemiology regulatory strategy and communicate with FDA and other Health Authorities in meetings as required<br>
•	Ability to understand the market and regulatory challenges for Takeda products; and to critically review competitors' data and assimilate pharmacoepidemiology strategies that take such environments into consideration.<br>
•	Excellent qualitative and quantitative pharmacoepidemiology skills, including with regards to study design and analysis of health insurance claims and other automated healthcare databases.<br>
•	Familiarity with SAS or similar software for data manipulation and data tabulation<br>
•	Excellent problem-solving and interpersonal skills are required, as are a high degree of self-motivation, initiative and attention to detail.<br>
•	Ability to work independently as well as in a team, and to manage multiple projects under tight deadlines are also essential.<br>
•	Setting goals, supervising, and evaluating performance of staff as well as planning growth of personnel.<br>
•	Excellent scientific writing, technical skills.<br>
 <br>
TRAVEL REQUIREMENTS:<br>
30% Required Domestic and International travel.]]></description>
<dc:date>2009-12-15T10:40:48-06:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://chicago.craigslist.org/nwc/sci/1511158317.html</dc:source>
<dc:title><![CDATA[Sr. Manager, Pharmacoepidemiology &amp; Epidemiology (Deerfield Park, Illinois)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-12-15T10:40:48-06:00</dcterms:issued>
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