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The Study Grant Analyst I at Parexel is responsible for preparing accurate and competitive clinical study grants, collaborating on budget concepts, and ensuring compliance with regulations and internal policies. They must possess strategic thinking skills, analytical abilities, and excellent communication skills. Ideal candidates will have 1-2 years of experience in clinical site budget development within the healthcare or pharmaceutical industries.
The Principal Biostatistician works independently on all level complexity clinical trial projects, often with major regulatory impact. Responsibilities include providing statistical support, leading production and quality control, performing sample-size calculations, and contributing to the development of internal and external statistical training seminars.
Execute application development tasks, coordinate integration services, product implementation and software updates. Function as a project team member or technical project manager. Analyze complex business requirements and provide technical solutions. Mentor junior staff members and ensure project targets are met effectively.
Accurate budget template setups based on contractual agreements, collaborate with internal teams for information, update budget templates as needed, ensure documentation is complete, submit ticket requests for payee setups, maintain knowledge of company procedures
Produce tables, figures, and data listings using efficient programming techniques. Perform statistical analyses under close supervision. Assist in the production of statistical reports and sections of integrated clinical reports. Check own work for quality. Communicate process improvement ideas. Travel to client meetings. Additional responsibilities as defined by supervisor. Good analytical skills, professional attitude, attention to detail.
Providing basic maintenance and support services for systems, troubleshooting system issues, monitoring and managing application services, knowledge of SQL, and administering enterprise applications.
The Study Grant Analyst II at Parexel is responsible for preparing accurate and competitive clinical study grants, collaborating on budget concepts for pre-sales proposals, and ensuring compliance with regulations and internal policies. This role involves analyzing grant information, participating in strategy sessions, and maintaining client-focused analysis to identify and resolve issues proactively.
An Analyst working in Applications Support at Parexel responsible for troubleshooting, system monitoring, and resolving issues related to Veeva Vault applications. Must have advanced system administration skills, knowledge of ITL processes, and experience with Service Desk Tools.
Act as an internal Subject Matter Expert and work independently to support various programming activities related to analysis and reporting of clinical study data. Perform as Statistical Programming Coordinator on projects and interact with Sponsors, Data Operation Lead, and other functions. Use efficient programming techniques to produce and QC derived datasets and TLF. Create/modify standard macros and applications to improve efficiency. Develop wider knowledge of SAS and other relevant programming languages and processes. Provide relevant training and mentorship to staff and project teams.
Senior Statistical Programmer role at Parexel focusing on project management, statistical programming for assigned projects, training, and maintaining regulatory compliance. Responsibilities include coordinating project activities, reviewing analysis plans, delivering high-quality service, and providing training and consultancy. Required skills include analytical skills, proficiency in SAS, knowledge of regulatory standards, and the ability to learn new systems.
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