PAREXEL International Corporation Jobs in California

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25 PAREXEL International Corporation jobs in California found on Monster.

Jobs 1 to 20 of 25
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 : 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 : 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 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 The Nurse Manager ensures that all clinical research studies conducted at PAREXEL Los Angeles Early Phase units are performed in compliance with all sponsor protocols; Good Clinical Practices (GCPs), Good Documentation Practices (GDP), Standard Operating Procedures (SOPs), and any other applicable regulations. The Nurse Manager will directly oversee the staff...
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 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 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 • 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 : 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...
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 : 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, PAREXE...
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 Manager contributes to and leads strategic initiatives for the structure and development of a Programming team in order to achieve the overall goals and mission of Global Technical Services. The Manager’s primary function is to provide direct project and team oversight. General responsibilities include supervision and management of staff; ensuring staff are adequately traine...
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 : The Senior 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 analysis and reporting. • Coordinate project start-up activities, including Unix/PMED project area set-u...
Job Description : The Project Financial Analyst III develops guides and supports the project analysis requirements for defined projects. Defines, drives and progresses all planning and development of financial project metrics. In addition, is responsible for alternative finance scenarios with a high degree of technical knowledge, business acumen, best practice approach and minimal supervision. As...
Job Description : •Provides advice and recommendations to the clinical departments regarding application of good clinical practice guidelines and industry guidelines pertaining to the regulatory requirements/aspects of clinical trials. •Prepares Form FDA 1572s, obtains necessary signatures, and compiles the required attachments in accordance with applicable regulations. •Photocopies and distrib...
Job Description : The Associate Director / Director is responsible for the oversight of a team of high level individual contributors or a group of Managers. This includes ensuring successful delivery of his/her organization’s project deliverables, on time with high quality. The Associate Director / Director is responsible to resource client projects with suitably developed professionals and to re...

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