PAREXEL International Corporation Jobs in California

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26 PAREXEL International Corporation jobs in California found on Monster.

Jobs 1 to 20 of 26
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 : 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...
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 : 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 Shipping Coordinator ensures that all inventory, storage and shipping of samples of clinical research studies conducted at the PAREXEL Glendale Early Phase Clinical Unit (EPCU) are performed in compliance with all sponsor protocols, Good Clinical Practices (GCPs), EPCU Standard Operating Procedures (SOPs), International Air Transport Association ( IATA) Dangerous Goods Regul...
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 : Key Accountabilities 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. • Recruits study participants by calling the database, attending company sponsored community events, posting flyers in schools, senior centers, supermarkets, and other establishments. • Ent...
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 : 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 : 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 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 : 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 : 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 : Essential Function The software engineer will be responsible for the design and development of the Electronic Data Capture suite of products in the life sciences industry. He/she must be comfortable supporting and maintaining existing applications by resolving software defects, implementing enhancements, and designing new software features. Qualifications : Job Qualifications...
Job Description : Key Accountabilities Plan day to day intermittent and temporary staff at the Clinical Operations to ensure sufficient resources. Meets regularly with Clinical Operations Managers to discuss staffing for upcoming studies, sharing of staff between departments, identifying cross functionality usage and driving trainings and/or other developmental needs as appropriate. Generates ...
Job Description : Essential Function Organize, execute, and coordinate the enrollment process of clinical research studies, including all activities from recruitment to admission. Ensure that protocols are implemented and followed according to Good Clinical Practice. Collect and organize research data. Educate participants about treatments and possible side effects and complications. Key Accoun...
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 : 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...

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