var xmlString = '<JobSearchResults LookID="centerwatch">  <!-- Served from  -->  <QueryString>clientid=centerwatch&amp;stringVar=xmlString&amp;pageSize=15&amp;searchType=featured&amp;outFormat=jsxml</QueryString>  <Jobs>        <Job>         <JobID>44783122</JobID>         <Title>CRA II - North East Region</Title>         <Employer>PPD, Inc         </Employer>         <Location>Washington, District of Columbia</Location>         <Description><![CDATA[North East region includes: CT, DE, KY, MA, ME, MD, NC, NH, NJ, NY, OH, PA, RI, TN, VT, VA, WV The Clinical Research Associate (CRA) performs and coordinates all aspects of the clinical monitoring and site management process in accordance with ICH Good Clinical Practices, FDA guidelines, local regulations and PPD Standard Operating Procedures. Conducts site visits to assess protocol and regulatory compliance and manages required documentation Responsible for ensuring that data will pass international quality assurance audits. Represents PPD in the global medical research community and develops and maintains collaborative relationships with investigational sites. Required to travel 60-80% on average. Education and Experience:Bachelor\'s degree in a science related field or a Registered Nursing certification or equivalent certification/licensure from an appropriately accredited institution Previous experience as a clinical research monitor that provides the knowledge, skills, and abilities to perform the job (comparable to one year) or completion of PPD Drug Development Fellowship.Valid Driver\'s License where applicableIn some cases an equivalent combination of education, professional training, and experience that provides the required Knowledge, Skills and Abilities may be considered Knowledge, Skills and Abilities:Proven clinical monitoring skillsDemonstrated understanding of medical/therapeutic area knowledge and medical terminologyDemonstrated ability to attain and maintain a working knowledge of Good Clinical Practices and applicable Standard Operating ProceduresGood oral and written communication skills, with the ability to communicate effectively with medical personnelCustomer focusGood organizational and time management skillsEffective interpersonal skillsAttention to detailProven flexibility and adaptabilityAbility to work in a team or independently as requiredGood computer skills: good knowledge of Microsoft Office and the ability to learn appropriate softwareGood English language and grammar skillsGood presentation skillsPPD is an Equal Opportunity Employer]]></Description>         <LookID>centerwatch</LookID>         <Url>http://centerwatch.careers.adicio.com/careers/jobsearch/detail/jobId/44783122/viewType/featured</Url>      </Job>        <Job>         <JobID>44783157</JobID>         <Title>Sr CRA - North East Region</Title>         <Employer>PPD, Inc         </Employer>         <Location>New York, New York</Location>         <Description><![CDATA[North East region includes: CT, DE, KY, MA, ME, MD, NC, NH, NJ, NY, OH, PA, RI, TN, VT, VA, WV The Clinical Research Associate (CRA) performs and coordinates all aspects of the clinical monitoring and site management process in accordance with ICH Good Clinical Practices, FDA guidelines, local regulations and PPD Standard Operating Procedures. Conducts site visits to assess protocol and regulatory compliance and manages required documentation Responsible for ensuring that data will pass international quality assurance audits. Represents PPD in the global medical research community and develops and maintains collaborative relationships with investigational sites. Required to travel 60-80% on average. Education and Experience:Bachelor\'s degree in a science related field or a Registered Nursing certification or equivalent certification/licensure from an appropriately accredited institutionPrevious experience as a clinical research monitor (comparable to 2+ years) that provides the required knowledge, skills and abilitiesValid Driver\'s License where applicableIn some cases an equivalent combination of education, professional training, and experience that provides the required knowledge, skills and abilities may be considered Knowledge, Skills and Abilities:Effective clinical monitoring skillsDemonstrated understanding of medical/therapeutic area knowledge and medical terminologyExcellent understanding and demonstrated application of Good Clinical Practices and applicable Standard Operating ProceduresEffective oral and written communication skills, with the ability to communicate effectively with medical personnelStrong customer focusEffective interpersonal skillsStrong attention to detailEffective organizational and time management skillsProven flexibility and adaptabilityAbility to work in a team or independently as requiredGood computer skills: good knowledge of Microsoft Office and the ability to learn appropriate softwareGood English language and grammar skillsGood presentation skillsPPD is an Equal Opportunity Employer]]></Description>         <LookID>centerwatch</LookID>         <Url>http://centerwatch.careers.adicio.com/careers/jobsearch/detail/jobId/44783157/viewType/featured</Url>      </Job>        <Job>         <JobID>44783146</JobID>         <Title>Sr Project Manager - Hematology/Oncology Division - Homebased</Title>         <Employer>PPD, Inc         </Employer>         <Location>Boston, Massachusetts</Location>         <Description><![CDATA[The Senior Project Manager (SPM) is responsible for the overall coordination and management of clinical trials from start up through close out activities.  Directs the technical and operational aspects of the projects -- thus securing the successful completion of clinical trials.  Works with major functional area leads to identify and evaluate fundamental issues on the project, interpret data on complex issues, make good business decisions and ensure solutions are implemented.  Works to ensure that all project deliverables meet the customer\'s time/quality/cost expectations. The SPM, with support from the Project Management Directors and/or Associate Directors, working in collaboration with other functional area leads, is accountable for ensuring that all project deliverables meet the customer/contract expectations, providing accurate hour forecasts, reviewing pass through costs and ensuring timely invoicing. In addition, SPMs may work with Directors and/or Associate Directors, Project management and Contracts & Proposals Development on the development of new proposals and general capabilities presentations to Customers for new business. Education and Experience:Bachelor\'s degree or licensed certified health care training or equivalent combination of education and experienceHas an in-depth understanding and extensive experience working within clinical development (equivalent to five years). This could include specific experience in a particular functional areaCan demonstrate experience successfully managing and/or leading large groups or teamsExperience using project management softwareSolid understanding of how to craft and manage a project budgetMust possess a valid passport, as appropriate Knowledge, Skills and Abilities: Possesses a high level of the following skills and attributes:       Knowledge of the key principles of cross functional project management (Time, Quality, Cost)Solid financial acumenApplies a range of negotiation techniques to achieve desired outcomes with evidence of commercial and organizational acumenDisplays effective communication skills (listening, oral, written) and can communicate in English language (oral, written)Sound interpersonal skills, is flexible and adapts to changing situationsHas the ability to persuade, convince, and influence or impress othersIs organized, proficient at multi-tasking with good attention to detailAble to lead, motivate and coordinate teams.  Coach/mentor team members as appropriateAble to delegate, effectively prioritizes own and workload of project team membersAbility to effectively use automated systems and computerized applications such as Outlook, Excel, Word, etcPossesses cross cultural awareness and is able to adapt appropriatelyHas an in-depth understanding and appreciation of clinical research/development, including medical and therapeutic areas, phases and medical terminologyHas experience with leading, liaising and coordinating cross-functional project teamsHas an in-depth knowledge/understanding of clinical development guidelines and DirectivesPPD is an Equal Opportunity Employer]]></Description>         <LookID>centerwatch</LookID>         <Url>http://centerwatch.careers.adicio.com/careers/jobsearch/detail/jobId/44783146/viewType/featured</Url>      </Job>        <Job>         <JobID>44783120</JobID>         <Title>Sr CRA - North East Region</Title>         <Employer>PPD, Inc         </Employer>         <Location>Boston, Massachusetts</Location>         <Description><![CDATA[Position requires a minimum of 2 years of traveling site monitoring experience.  Seeking homebased candidates currently residing in CT, DE, KY, MA, ME, MD, NC, NH, NJ, NY, OH, PA, RI, TN, VT, VA, WV The Sr. Clinical Research Associate (CRA) performs and coordinates all aspects of the clinical monitoring and site management  process in accordance with ICH Good Clinical Practices, FDA guidelines, local regulations and PPD Standard Operating Procedures. Conducts site visits to assess protocol and regulatory compliance and manages required documentation Responsible for ensuring that data will pass international quality assurance audits. Represents PPD in the global medical research community and develops and maintains collaborative relationships with investigational sites and client company personnel. May assist project manager or clinical team manager on assigned projects. Required to travel 60-80% on average.   Education and Experience:Bachelor\'s degree in a science related field or a Registered Nursing certification or equivalent certification/licensure from an appropriately accredited institutionPrevious experience as a clinical research monitor (comparable to 2+ years) that provides the required knowledge, skills and abilitiesValid Driver\'s License where applicableIn some cases an equivalent combination of education, professional training, and experience that provides the required knowledge, skills and abilities may be considered Knowledge, Skills and Abilities:Effective clinical monitoring skillsDemonstrated understanding of medical/therapeutic area knowledge and medical terminologyExcellent understanding and demonstrated application of Good Clinical Practices and applicable Standard Operating ProceduresEffective oral and written communication skills, with the ability to communicate effectively with medical personnelStrong customer focusEffective interpersonal skillsStrong attention to detailEffective organizational and time management skillsProven flexibility and adaptabilityAbility to work in a team or independently as requiredGood computer skills: good knowledge of Microsoft Office and the ability to learn appropriate softwareGood English language and grammar skillsGood presentation skillsPPD is an Equal Opportunity Employer]]></Description>         <LookID>centerwatch</LookID>         <Url>http://centerwatch.careers.adicio.com/careers/jobsearch/detail/jobId/44783120/viewType/featured</Url>      </Job>        <Job>         <JobID>44523701</JobID>         <Title>Regional Home-Based CRAs</Title>         <Employer>DOCS - ICON Resourcing Solutions         </Employer>         <Location>Miami, Florida</Location>         <Description><![CDATA[DOCS has several Regional Home-Based CRAs openings in Ft. Lauderdale, FL and Miami, FL.  The Role and Your Responsibilities You will be responsible for providing effective scientific and technical expertise in the execution of clinical studies that meet protocol objectives, all applicable Sponsor standards, Good Clinical Practices, and regulatory requirements. The job requirements and skills include:Initiate, Monitor and Close out study sitesProvide quality databases in an efficient and expeditious mannerCommunicate and provide timely and accurate progress reportsIdentify and resolve problems regarding site performance and processesEnhance productivity, adding value to assigned tasks and developing technical skills and expertise in the conduct of clinical trialsPosition requires up to 70% travelSites are located in Miami and Ft. Lauderdale, FLEach CRA will manage approximately 12-14 sitesFLEXIBILITY is key!Must be 100% dedicated to sponsor   What is required? BA/BS with six or more years of clinical research experience including five years of direct CRA experienceTypical training includes course work on good clinical practices, monitor training, clinical reporting and FDA regulations.Therapeutic areas are CNS, Cardiovascular, Hypertension, Respiratory and Diabetes.Must live in Ft. Lauderdale or Miami areas. What is Offered  DOCS clients include small, mid and large sized Pharmaceutical companies in addition to many leading Biotechnology, Medical Device companies and CROs. As a global partner, DOCS currently offers global resourcing solutions to our clients.  We offer competitive salary, comprehensive benefits including paid days off, 401K and health insurance.    Why this Vacancy is right for you  You are an experienced CRA seeking a new project with a stable organization. You have the ability to travel and understand the complexity of monitoring clinical trials.   ICON Clinical Research is an Equal Opportunity Employer committed to strength in diversity.   Apply to: Kristina.Serrano@docsglobal.com]]></Description>         <LookID>centerwatch</LookID>         <Url>http://centerwatch.careers.adicio.com/careers/jobsearch/detail/jobId/44523701/viewType/featured</Url>      </Job>        <Job>         <JobID>44783135</JobID>         <Title>CRA II - North East Region</Title>         <Employer>PPD, Inc         </Employer>         <Location>Philadelphia, Pennsylvania</Location>         <Description><![CDATA[North East region includes: CT, DE, KY, MA, ME, MD, NC, NH, NJ, NY, OH, PA, RI, TN, VT, VA, WV The Clinical Research Associate (CRA) performs and coordinates all aspects of the clinical monitoring and site management process in accordance with ICH Good Clinical Practices, FDA guidelines, local regulations and PPD Standard Operating Procedures. Conducts site visits to assess protocol and regulatory compliance and manages required documentation Responsible for ensuring that data will pass international quality assurance audits. Represents PPD in the global medical research community and develops and maintains collaborative relationships with investigational sites. Required to travel 60-80% on average. Education and Experience:Bachelor\'s degree in a science related field or a Registered Nursing certification or equivalent certification/licensure from an appropriately accredited institution Previous experience as a clinical research monitor that provides the knowledge, skills, and abilities to perform the job (comparable to one year) or completion of PPD Drug Development Fellowship.Valid Driver\'s License where applicableIn some cases an equivalent combination of education, professional training, and experience that provides the required Knowledge, Skills and Abilities may be considered Knowledge, Skills and Abilities:Proven clinical monitoring skillsDemonstrated understanding of medical/therapeutic area knowledge and medical terminologyDemonstrated ability to attain and maintain a working knowledge of Good Clinical Practices and applicable Standard Operating ProceduresGood oral and written communication skills, with the ability to communicate effectively with medical personnelCustomer focusGood organizational and time management skillsEffective interpersonal skillsAttention to detailProven flexibility and adaptabilityAbility to work in a team or independently as requiredGood computer skills: good knowledge of Microsoft Office and the ability to learn appropriate softwareGood English language and grammar skillsGood presentation skillsPPD is an Equal Opportunity Employer]]></Description>         <LookID>centerwatch</LookID>         <Url>http://centerwatch.careers.adicio.com/careers/jobsearch/detail/jobId/44783135/viewType/featured</Url>      </Job>        <Job>         <JobID>43189679</JobID>         <Title>Clinical Research Coordinator</Title>         <Employer>Confidential         </Employer>         <Location>Las Vegas, Nevada</Location>         <Description><![CDATA[Job DescriptionNeed ASAP an experienced Clinical Research Coordinator to work Part time or Full Time in an Internal Medicine research office.  Must have clinical research experience, no exceptions, have worked with EDC\'s, and know about regulatory binders.  This is a small office that supports a teamwork atmosphere.  Also, must have BLS certification, and must have a good work ethic and love patient care! Also, must be excellent with blood draws, performing EKG\'s, and shipping out samples to central laboratories.]]></Description>         <LookID>centerwatch</LookID>         <Url>http://centerwatch.careers.adicio.com/careers/jobsearch/detail/jobId/43189679/viewType/featured</Url>      </Job>    </Jobs></JobSearchResults>';