Search the 25 jobs at Parexel

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.

Principal Biostatistician at Parexel responsible for providing expertise in statistical methods, representing Biostatistics and Parexel, participating in business development, managing quality issues, and more. Requires Ph.D. or master's degree in statistical science with 6 years of relevant experience. Proficiency in SAS programming and knowledge of regulatory guidance and standards.

Support Account Team for Successful Project Delivery by providing skilled support in project implementation and management. Assist with QC, fact-checking, financial tracking, and client publication tracking. Coordinate meetings, maintain project tracking materials, and assist with document formatting and submissions. Serve as a super-user for databases and assist with permissions process.

CTSL Sourcing Specialist at Parexel responsible for managing formal and complex RFI/RFQ/ RFP processes, verifying purchase requests, ensuring budgeted pricing, coordinating returns, managing sourcing queue, and invoice reconciliation. Requires understanding of Clinical Studies and related Supply Chain aspects, procurement and contracting principles, and GxP regulatory framework.

Design, build, modify, and support data pipelines using Microsoft Azure data PaaS services like DataBricks and PowerBI. Collaborate with Team Leads, run tests, benchmark code, troubleshoot issues, mentor staff, and manage technical delivery. Requires 11-20 years of software development experience with at least 5 years in cloud computing and 1+ years in DataBricks, Synapse, or Snowflake.

The Biostatistician II at Parexel contributes to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions. Responsibilities include leading statistical aspects for studies, participating in protocol reviews, providing data interpretation, developing trial designs, and communicating effectively with partners and opinion leaders.

The Biostatistician I at Parexel contributes to the statistical analysis, interpretation, and reporting of clinical trial data. Responsibilities include developing statistical methods, reviewing data, and contributing to regulatory responses and publications. This role requires a degree in Statistics and a minimum of 3 years of industry experience.

Statistician with 5-8 years of experience in clinical studies providing statistical inputs, sample size calculation, protocol design, and manuscript writing. Proficient in SAS for statistical activities and report preparation.

As a Senior Financial Analyst at Parexel, responsible for communication, analytics, problem-solving, driving results, financial acumen, partnering for business success, and process & project management. Thrives in a fast-paced environment, strong in financial management, clinical research, and interpersonal skills.

Parexel is looking for a Senior Software Engineer to develop low-code applications in the Clinical domain using Microsoft Power Platform. The role involves analyzing, designing, coding, testing, and maintaining low-code applications, as well as mentoring other developers in low-code development. The candidate should have 5+ years of development experience, Agile Methodology experience, and strong communication skills.

The Senior EBS Developer at Parexel is responsible for working with Oracle EBS Finance 12.2.4 systems functions and other finance-related systems to align with business objectives. They will develop and manage application solutions for finance systems within the organization.