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

Schedule, coordinate, assist with external and internal meetings and communications of assigned senior managers. Work closely with admin leader and line manager to keep them well informed of upcoming commitments and responsibilities, following up appropriately. Manage expense records and assist with reimbursement. Coordinate flights, accommodations, visas, and all logisti

Key Accountabilities Manage Projects & Technology Lead and implement the setup of Data Receipt Agreements with vendors by working with cross functional teams. Programming and setup of Import procedures to allow the ingestion of data either using SAS or alternative technology (e.g. "Workbench"). Programming of reconciliation checks to ensure appropriate transfer of data. P

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

Providing meals to subjects Coordination and ordering food from caterer for volunteers in cooperation with the study team Distribute food and beverages to study participants according to study protocol and internal requirements Supervise volunteers during mealtimes, assisting them with catering requirements as required Ensuring menus have macro nutrients checked by the Di

Parexel is one of the only CROs to provide a broad depth of Clinical Pharmacology, Modeling and Simulation (CPMS) expertise to our clients, and the group is growing its capabilities and expanding globally!We currently havetremendous opportunities available to join this extremely collaborative and super friendly team! If you're looking for an opportunity to expand professi

Parexel Early Phase Clinical Unit supports the development of innovative new medicines which are vital for public health, improving outcomes, and saving lives. The early phase and "first in human" trials are the first step in testing these novel treatments in humans. At Parexel's Glendale, CA unit our highly trained and skilled Patient Recruitment Coordinator are crucial

Clinical Operations Leader / Clinical Trial Manager team members at Parexel average close to 10 years with the company and we are expanding our team. We currently have Home Based Clinical Operations Leader/Clinical Trial Manager positions available in the US. As the Clinical Liaison to the Project Leader, the COL/CTM leads the clinical aspect of the trial and has a direct

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. Job Title Conference & Meeting Coordinator Job Introduction At Parexel, we are a leading Clinical Research Organization (CRO) company specializing in delivering life changing medicines to patients. We are seeking a Confere

Key Accountabilities Start up (from site identification through pre initiation) Act as Parexel's direct point of contact with assigned sites, accountable for quality and delivery during the start up phase. Build relationships with investigators and site staff. Conduct, drive and manage country specific feasibility and/or site pre qualification and qualification activities

At Parexel you'll team up with some of the best minds in the industry to get new treatments to the patients who need them most. Parexelis one of the largest providers of medical writing services worldwide and has managed thousands of writing projects in more than 29 countries in North and South America, Europe, Asia, and Africa. As a result of continued customer satisfact

Currently hiring a Principal Clinical Regulatory Medical Writer to work r emote from any location in the US. ( Full time) The Principal Medical Writer will research, create, and edit all documents associated with clinical research. The Principal Medical Writer may operate as the project lead writer/submission coordinator and primary client contact to manage contributions

Act as senior therapy area/content expert and lead the delivery of assigned programs/projects within account team, interacting directly with client and KOLs Develop high quality scientific content by means of all necessary research, scientific writing, editing, and fact checking, to meet deadlines while working within project scope and objectives. Applies to all formats o

Do you want to make an impact in your next role? 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. Parexel is seeking an experienced Workday HCM Compensation Implementation Specialist to join our HR Systems team. As an HCM Compensation SME, you will be responsible f

Senior Regulatory Affairs Associate Experience Biologic CMC 5+ years of experience Supported the CMC activities related to Vaccine/Biologic manufacturing and control including authoring of submission dossiers related to new application, post approval variations Understanding of EU/CA/WHO/US regulations & guidance allowing appropriate review and compilation of data to appr