The Clinical Finance Systems Analyst (CFSA) is responsible for clinical financial and accounting processes, such as data system set up, payment systems administration, processing invoices, payments to investigators and vendors, reconciling site payments, and performing data migration and validation between payment applications. Job Description Prepares and uploads data to

Parexel is looking for changemakers who are driven by curiosity, passion, and optimism. Come join us in keeping the Patient at the Heart of Everything We do. Job Title Principal Workday Time Functional Analyst IT HR Systems Job Introduction At Parexel, we are a leading Clinical Research Organization company specializing in delivering life changing medicines to patients. W

The Senior Medical Writer is responsible for the development of medical writing deliverables that support the clinical regulatory writing portfolio and works with guidance and oversight to achieve goals. Key Accountabilities Leadership Leads cross functional teams to draft agreed upon scientific/medical content that addresses data interpretation, product claims, and inter

Home Based, US As a Site Contract Leader with Parexel you will manage the entire Clinical Site Agreement (CSA) process for a number projects, including the development of the study specific CSA strategy with the Sponsor, preparation of the corresponding country specific CSA templates and country specific budgets and also negotiation of such CSAs and budgets with the indiv

We are seeking an experienced Regulatory Generalist to join our FSP team as a Senior Regulatory Affairs Associate / Regulatory Affairs Consultant to work closely with one large, dedicated client and provide operational support in the IND/NDA maintenance stage. The Sr. Associate / Consultant will also provide appropriate regulatory guidance to Project Teams for the develop

Your time here As an experienced Biostatistician, you will lead research design and analytical strategies, provide input into protocols, develop and review statistical analysis plans and author/co author reports, abstracts and manuscripts. You will use your knowledge to advise, provide guidance and to oversee the quality control of statistical deliverables. As the functio

Home Based, US As a Site Contract Associate you will oversee the site contracting process for clinical trials, ensuring that contracts are executed in a timely and effective manner. This is a client facing role with both sponsors and team projects. Accountabilities Monitor, drive, and report on site contract performance throughout the whole lifecycle, specifically metrics

Home Based, US As a Parexel Contract Manager (in Commercial Operations/Sales) your role is to ensure consistent management of all contracts through "management" of the contract management process, development of account specific standards, documentation and negotiations. The Contract Manager serves as the Client's primary interface regarding contractual issues. Key Accoun

Parexel has an exciting new position for a seasoned Clinical Research Professional with a strong background in client and clinical program management along with pre award strategy and bid development to join our global team as a Solutions Consulting Director Oncology. The Solution Consulting Director will be a recognized professional in their area (technical, functional o

Parexel has an exciting new position for a seasoned Clinical Research Professional with a strong background in client and clinical program management along with pre award strategy and bid development to join our global team as a Solutions Consulting Director Infectious Disease/Immunology. The Solutions Consulting Director will be a recognized professional in Infectious Di

Join Parexel's team of changemakers as we help advance healthcare throughout the globe, all while keeping the patient at the heart of everything we do. At Parexel, we are a leading Clinical Research Organization (CRO) company specializing in delivering life changing medicines to patients. We are seeking a Senior Quality Assurance Auditor to join our team. Our Senior Quali

Parexel's Regulatory Consulting team is known for our unparalleled breadth and depth of expertise globally. Parexel Regulatory Consulting offers services which create and maximize product value for clients throughout the product lifecycle, leveraging our unique fusion of scientific, regulatory, and business expertise. We are the pre eminent regulatory and GxP (Good Clinic

Home Based, US As a Sr Quality Manager in Technology Quality Management (TQM) you will manage efforts to define, adopt and oversee compliance to processes and standards as the fundamental baseline for technology solution development, validation and delivery. You will support efforts, in collaboration with the business to monitor, identify and implement continuous process

The Senior Vice President, Real World Evidence Operations, is responsible for development and execution of strategies to enable profitable RWE operations business growth Against revenue, margin and new business targets Through delivery of a portfolio of studies incorporating primary and secondary use of RWD to generate RWE; RWD licensing, access and provision; As a centre

Parexel is one of the only CROs to provide a broad depth of Clinical Pharmacology, Modeling and Simulation expertise to our clients, and the group is currently seeking an intellectually curious and highly innovative Clinical Pharmacology / PK Director to bring their high level of motivation to our team and help our clients reduce the time to bring new treatments to patien