The Bilingual Research Associate will support clinical trials by recruiting participants, conducting screenings, maintaining study logs, and ensuring participant safety. Responsibilities include managing study supplies, assisting physicians, and complying with clinical guidelines. This is a per diem position requiring flexibility and availability for various shifts after an initial training period.

The Senior Accountant - Finance at Parexel is responsible for US GAAP and Statutory Accounting including day-to-day local GAAP accounting, preparing tax filings, balancing sheet reconciliations, ensuring compliance with statutory requirements, and supporting audits. The role requires interaction with various teams and proficiency in Oracle ERP.

As a Clinical Research Associate, you'll select clinical institutions and physicians, contract clinical trials, oversee drug logistics, monitor compliance with protocols, perform source data verification, submit documents to IRBs, and ensure necessary documents are properly stored.

The Senior Quality Assurance Auditor will lead, plan, perform, and report GxP audits across all phases of Clinical Research, ensuring compliance with Good Practices. Responsibilities include mentoring staff, optimizing processes, supporting investigations, and providing consultancy on regulatory compliance.

As a Senior Software Engineer at Parexel, you will focus on automating testing and DevOps with Microsoft Azure PaaS services, design and support data pipelines using DataBricks and PowerBI, run unit and integration tests, assist with troubleshooting, and collaborate with teams to define requirements and address application issues.

The RPA Support Engineer at Parexel will design, develop, and maintain automation solutions using UiPath. Responsibilities include defining automation requirements, developing bots, testing scenarios, and providing production support throughout the automation lifecycle while adhering to security best practices.

The Events Specialist at Parexel is responsible for planning, executing, and managing logistics for global conferences and events, coordinating speaker arrangements, and evaluating event success through feedback and data analysis. This role requires interaction with senior executives, budget management, and oversight of promotional efforts associated with events.

The Statistical Programmer II at Parexel will assist in project management, deliver high-quality statistical programming for clinical projects, and provide training and mentorship to staff. Responsibilities include producing datasets, ensuring regulatory compliance, and participating in quality improvement initiatives. The role requires proficiency in SAS and strong analytical skills.

Responsible for negotiating study-specific Clinical Site Agreements (CSA) and budgets with sponsors. Oversee CSA activities, coordinate with local teams, and ensure compliance with regulatory requirements. Facilitate training, resolve negotiation issues, and maintain project status reports, ensuring timely communication and high-quality work.

The Financial Analyst II at Parexel will provide financial analysis and reporting to project leadership, assist in budgeting and revenue cycle management, produce financial metrics, and support resource planning across assigned projects. The role demands effective communication and an analytical approach to manage financial operations and address scope changes.

As a Senior Software Engineer (Frontend) at Parexel, you will design, develop, and maintain web applications, lead technical innovations, and collaborate with cross-functional teams to deliver innovative solutions from inception to implementation.

The Biostatistician II at Parexel will produce and QC datasets, apply advanced statistical methods, and lead project teams to meet client needs. Responsibilities include mentoring junior staff, ensuring quality, and supporting business development activities alongside training clients in statistical analysis and attending client meetings to present results.

The Bilingual Research Associate will support clinical trials by recruiting participants, conducting screenings, and managing study logistics. Responsibilities include entering participant data, assisting with medical assessments, ensuring participant safety, and maintaining study documentation. This role emphasizes customer service and the ability to manage multiple tasks in a clinical research environment.

The Study Start-Up Leader is responsible for managing the study start-up strategy and ensuring timely delivery of start-up activities. This includes coordinating with global teams, developing activation strategies, and monitoring progress against timelines while identifying and mitigating risks.

The Site Contract Associate is responsible for drafting, reviewing, and negotiating site agreements. They ensure compliance with applicable regulations, manage contract execution, and maintain communication between site contracts staff and other stakeholders. The role requires a deep understanding of clinical trial protocols and aims to identify and resolve contracting issues effectively.

The Principal Business Operations Lead will manage and oversee internal projects in Real-World Research, develop PMO processes, drive improvements in project management, lead cross-functional teams, and ensure project compliance and quality control. This role requires strong stakeholder communication and the management of operational risks and metrics.

The Trial Master Files Record Specialist manages the Electronic Trial Master File (eTMF) for clinical trials, ensuring compliance with protocols and regulations, oversees record-keeping, supports trial teams, and contributes to audits and inspections. They maintain close communication with clinical trial teams and oversee the close-out process of trial master files after completion.

The Data Acquisition Specialist will lead the collection of non-CRF data for multiple clinical studies, ensuring data quality and adherence to standards. Responsibilities include collaborating with vendors, developing study plans, and effectively communicating with study teams on data deliverables and issues, while understanding regulatory compliance.

The Scientist III or Principal Scientist I will manage shipments and documentation for raw materials and drug products, maintain shipment tracking systems, liaise with project teams, support regulatory compliance, and troubleshoot logistics issues to ensure timely delivery of shipments.

The position at Parexel involves contributing to clinical development solutions aimed at improving health and helping patients. It emphasizes teamwork and a commitment to making a difference in health outcomes.