PAREXEL International Corporation Jobs in California

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28 PAREXEL International Corporation jobs in California found on Monster.

Jobs 1 to 20 of 28
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 : Provide quality oversight to project team management throughout the project. Specifically responsible for standard and risk-based quality interventions including: review of key project documentation, consultation, CAPA support, audit and inspection support, and collection and reporting of project quality metrics. Key Accountabilities • Implement the standard quality interventi...
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 : 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 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 : 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 : 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 : 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 : The Principal Biostatistician works independently on all level complexity clinical trial projects, often with major regulatory impact. The person will be recognized internally and externally as a statistical expert. The Principal will lead projects and drive timelines and deliverables within the team. Key Accountabilities Provide broad statistical support, including trial desi...
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)...
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 : 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 : This Clinical Research Coordinator (CRC) position will focus on projects associated with functional Magnetic Resonance Imaging (fMRI) of the brain in combination with neuropsychological tests. The CRC will conduct fMRI studies in volunteer research subjects, administering stimulus presentations and working with associated software. Qualifications Bachelor's Degree in neuroscie...
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 : 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 : Essential Function The Research Nurse Practitioner (NP) functions under the direction and guidance of a licensed physician. The NP at the Los Angeles facility is responsible for review of health history, physical assessment, laboratory assessment indices and clinical tests of potential study participants for the purpose of qualifying participants for studies. The NP diagnoses h...
Job Description : Essential Function Lead the PAREXEL and Client teams by combining a depth of clinical research experience with insight into client pressures and an ability to develop the right solution for the client. This requires in-depth business understanding in order to make effective decisions independently and the knowledge and experience required to confidently recommending a course of...
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 San Diego, California, as a Clinical Trial Specialist (CTS) you will conduct and f...
Job Description : The EPD PS is responsible for supporting the EPD Project Leader (PL) and the project team with the set-up, initiation, planning, execution, control/maintenance and closure of EPD Projects (clinical trials) according to PAREXELs SOPs, tools, templates, systems and guidelines. Ability to: • Plan, organize, prioritize and meet deadlines • Analyze and consolidate large amounts of...
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...

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