PAREXEL International Corporation Jobs in Durham

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23 PAREXEL International Corporation jobs in Durham, North Carolina found on Monster.

Jobs 1 to 20 of 23
Job Description : Job Title Associate Director, Site Intelligence Department Feasibility and Enrollment Solutions SBU Clinical Research Services Location RTP Essential Function: The associate director is responsible for the oversight of a team or group of high-level individual contributors. This includes ensuring successful performance and delivery of his/her direct reports project deliverab...
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 : Key Accountabilities: -Recruit, retain and develop a skilled, experienced and motivated team of Project Assistants and Project Specialists. -Manage the performance, development and growth of Project Assistants and Project Specialists; developing appropriate orientation/induction program, ensure timely and accurate performance reviews, ensure up to date development plans for...
Job Description : The Data Operations Leader has overall accountability for the execution of the Data Operations strategy and the Data Operations’ Technology set-up for the project. The Data Operations Leader is providing overall leadership / management for programming, data integration, data processing and statistical services on a project / program. General areas of responsibility include: coor...
Job Description : The Data Operations Leader has overall accountability for the execution of the Data Operations strategy and the Data Operations’ Technology set-up for the project. The Data Operations Leader is providing overall leadership / management for programming, data integration, data processing and statistical services on a project / program. General areas of responsibility include: coor...
Job Description : A unique and exciting opportunity exists for an experienced Recruiter to join a growing, global organization. We are seeking a creative, hands-on recruiter to manage full-cycle recruitment for Clinical Research and Regulatory positions. The selected candidate will be expected to develop and implement strategic recruiting plans, manage vendors, utilize social networking and recru...
Job Description : Essential Function To perform administrative tasks proactively and to support EPD clinical operations staff (all levels) to the highest standards of quality and efficiency. Contributes to the smooth efficient running of the department. Qualifications : Key Accountabilities • Provide proactive administrative support for Clinical Operations Management staff (all levels) and EP...
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 has an exciting opportunity for a Director, Clinical Operations in either our Durham (RTP), NC or Billerica MA office. The Director is responsible to lead, manage and support the departmental or functional team and processes to ensure that PAREXEL delivers quality projects to its clients and achieves agreed revenue margins. Guide ongoing training, career development and ...
Job Description : PAREXEL values passion, global perspective and expertise and we are in the process of recruiting experienced Clinical Monitoring Associates to work in our Durham, North Carolina office. As PAREXEL’s remote contact with assigned clinical sites you will use judgment to assess and ensure overall integrity of study implementation and adherence to study protocol at clinical sites. Th...
Job Description : The role of the Senior Clinical Data Analyst (Sr CDA) is to manage the performance of clinical data processing activities from database set-up through database lock on assigned projects, commensurate with experience and/or project role. Responsible for project managing a moderate to large team or multiple small size protocols as the Primary CDA, with minimal to no supervision. A...
Job Description : Working from our office location in Durham, NC, as a Clinical Trial Specialist (CTS) you will conduct and facilitate specific start-up activities that may include site identification, feasibilities, essential document collection and review, ICF customization, EC submissions, preparation and negotiation of Clinical Site Contracts for site locations throughout the US. You must hav...
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 Biostatistician II works independently in the programming and quality control of derived datasets and all kind of statistical outputs (e.g., tables, listings and figures), works under the supervision of an experienced biostatistician in the production of analysis plans and reports, provides basic statistical advice to clients and fulfills the project primary role within a de...
Job Description : The Associate Director, Clinical Data Analyst 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 is responsible to resource client projects with suitably developed professionals and to r...
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 : 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 Senior Database 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 clinical systems, and/or the applications/systems within eClinical technologies. In addition, the...
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 role of the Clinical Data Analyst (CDA) is to independently perform all clinical data cleaning activities on assigned projects, commensurate with experience and/or project role. Responsible for coordinating a moderate to large team or multiple small size protocols as the CDA Coordinator, with minimal to no supervision. Alternatively, take on the role of a CMA/CDA Coordinato...

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