PAREXEL International Corporation Jobs in California

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22 PAREXEL International Corporation jobs in California found on Monster.

Jobs 1 to 20 of 22
Job Description : The Statistical Programmer II supports various programming activities related to analysis and reporting: Assist in the production and QC of derived dataset specifications and programming specifications Produce and/or QC derived datasets tables, figures and data listings Understand regulatory requirements concerning industry technical standards (e.g., CDISC, 21 CFR Part 11, el...
Job Description : Resolve complex technical problems as part of second level technical support. Analyze non-standard problems, develop technical solutions to meet each problem. Perform user training, work with other IT teams to develop and implement solutions. Provide support to hardware, software or application development efforts. Work with IT Service Desk to analyze and develop solutions to on...
Job Description : Serves as overall client relationship manager and strategic business partner, responsible for developing and expanding new business opportunities with customers. Oversees process of procurement of business, delivering top line business development performance for CRS, allowing PAREXEL and Clinical Research Services (CRS) to achieve or exceed targets. Responsibilities include: C...
Job Description : Essential Function Conduct and facilitate specific start-up activities such as site identification, feasibility, SRP collection, review and approval, perform ICF customization, IRB/EC and MoH/RA submissions, and/or negotiate Clinical Site Agreements (CSA) with a high accountability on quality and timelines. Key Accountabilities: Appropriately plan and meet site activations wi...
Job Description : Essential Function Perform the clinical monitoring aspect of designated projects in accordance with study specific procedures, applicable SOPs, and regulations. Act as PAREXEL’s direct contact with assigned clinical sites and use judgment to assess and ensure overall integrity of study implementation and adherence to study protocol at clinical sites. Responsibilities include...
Job Description : Including but not limited to the following and other duties as may be assigned: • Has detailed knowledge of the study protocols and acceptable performance of quizzes. • Enters study participants in the study participant tracking system, ClinCenter, and study logs, maintains appointment calendars, and operates company information systems and computer programs. • Conducts scree...
Job Description : The Senior Statistical Programmer provides technical expertise for the conduct of clinical trials, might act as an internal subject matter expert in specific areas providing technical support and expert advice, and works independently to support various programming activities related to the analysis and reporting of clinical study data. In addition, the Senior Statistical Progra...
Job Description : The responsibility of a Clinical Research Associate (CRA) is to perform the clinical monitoring aspect of designated projects in accordance with applicable SOPs. Responsibilities include performing clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, data collection), collecting regulatory documentation (when required)...
Job Description : PAREXEL International is a growing, fast-paced, global Clinical Research Organization (CRO) that has helped bring to market 49 of the top 50 selling pharmaceuticals. In fact, we have worked with all 10 of the world's top 10 pharmaceutical companies. Given our breath of expertise and the trust placed in us by pharmaceutical companies worldwide, PAREXEL can provide you with a numb...
Job Description : Key Accountabilities • Execute all appropriate Investigator responsibilities on assigned projects. • Serve as a Primary and Sub-Investigator on research protocols. • Support Standard Operating Procedures (SOPs), Good Clinical Practices, and all work processes to ensure efficient and compliant clinical operation. • Assist with the psychological and clinical oversight of all a...
Job Description : The Senior Biostatistician works independently in the production and quality control of analysis plans, reports, derived datasets, tables, listings and figures, provides statistical advice to clients and fulfills the project primary role within a designated project team. Key Accountabilities Coordinate and lead a project team to successful completion of a project within given ...
Job Description : Essential Function Perform the clinical monitoring aspect of designated projects in accordance with study specific procedures, applicable SOPs, and regulations. Act as PAREXEL’s direct contact with assigned clinical sites and use judgment to assess and ensure overall integrity of study implementation and adherence to study protocol at clinical sites. Responsibilities include...
Job Description : Including but not limited to the following and other duties as may be assigned: • Has detailed knowledge of the study protocols and acceptable performance of quizzes. • Enters study participants in the study participant tracking system, ClinCenter, and study logs, maintains appointment calendars, and operates company information systems and computer programs. • Conducts scree...
Job Description : The Senior Statistical Programmer provides technical expertise for the conduct of clinical trials, might act as an internal subject matter expert in specific areas providing technical support and expert advice, and works independently to support various programming activities related to the analysis and reporting of clinical study data. In addition, the Senior Statistical Progra...
Job Description : The Senior Auditor will have an in-depth understanding and knowledge of GCP compliance and other applicable regulations and laws, PAREXEL procedures and appropriate PAREXEL processes, which allows the individual to plan and conduct internal and external audits independently and to be able to mentor less experienced auditors. Auditors must be detail oriented, able to maintain a b...
Job Description : Key Accountabilities • Possesses thorough knowledge of all current Early Phase study protocols and design. • Develop, implement, monitor, and support Standard Operating Procedures (SOPs) and work processes to ensure the efficient clinical operation of the EPCU • Organizes the Clin-Ops meetings (which hands studies over from Business Development/Business Administration to Clin...
Job Description : Key Accountabilities -Lead the management team to ensure that resources (processes, procedures, personnel etc) optimally support the business requirements of the function • Ensure that the department has a well-organized infrastructure and adequate resources to enable projects to be completed on time and within budget. • Provide accurate forecasting figures for the annual bud...
PAREXEL International Corporation is a leading global bio/pharmaceutical services organization, providing a broad range of knowledge-based contract research, consulting, and medical communications services to the worldwide pharmaceutical, biotechnology and medical device industries. Committed to providing solutions that expedite time-to-market and peak-market penetration, PAREXEL has developed sig...
Job Description : Conduct and facilitate specific SSU activities such as feasibility, site identification, pre-qualification, SRP review and approval, ICF customization and negotiation (as needed) and IRB/EC preparation and submission, in accordance to local regulations, SOPs and Working from our office location in Billerica, MA, as a Clinical Trial Specialist (CTS) you will conduct and facilitat...
Job Description : The Manager is responsible to resource client projects with suitably developed professionals and to retain and develop these professionals within PAREXEL. The Manager may also be part of a project team and be responsible for successful delivery of his/her own project deliverables, on time with high quality. The Manager is responsible to promote new business by participating in p...

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