1 Inhouse CRA/ Remote CRA 1 CRC (Major site Oncology part CRC preferred) , . 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 sp

The Investigator Financial Analyst is expected to establish themself as a "co pilot", along with the Project Leader (PL) and Finance Business Partner (FBP), in steering the investigator budget management for a set of projects. As such, the IFA acquires an understanding of the investigator budget economic drivers. They assist in translating the clinical conduct into a fina

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

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

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

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

We are looking for a Azure Full Stack Developer for our office in Buenos Aires, Argentina. This position will working on the following activities Using Microsoft Azure data PaaS services, will design, build, modify, and support data pipelines leveraging DataBricks and PowerBI in a medallion architecture setting. If necessary, create prototypes to validate proposed ideas a

The Customer Strategy Director will drive the growth and innovation of Parexel Medical Communications. Serve as the client relationship lead and strategic business partner for prospective clients.Responsible for developing and expanding new business opportunities in liaison with Commercial and Subject Matter Experts (SMEs) across Parexel. Support the Account Management te

HRHRCompensation & Benefits, Employee Relations VISA HR HRCOECenter of ExpertiseOD 70 30 HR58 PC Excel VLOOKUP , If, Pivot Table Word, PowerPoint

We are looking to fill a microbiologist position working as a full time employee of Parexel FSP on long term assignment onsite at one of our clients in Rahway, NJ. Qualifications Bachelor's degree required; concentration in a scientific or applied discipline strongly preferred A minimum of 1 2 years of experience in a Pharmaceutical Microbiology related position required

We are looking to fill a microbiologist position working as a full time employee of Parexel FSP on long term assignment onsite at one of our clients in Rahway, NJ. Qualifications Bachelor's degree required; concentration in a scientific or applied discipline strongly preferred A minimum of 1 2 years of experience in pharmaceutical microbiology related position required (o

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We have an exciting opportunity for an Associate Qualified Person. You will provide direction to PLD, PM&D and LQM which includes mentoring and training of GxP relevant topics and the supervision of Quality Management projects. You will serve as a quality consultant to designated operational group(s) and will be responsible for Identification of process improvement opport

As a Pharmaceutical Services Specialist , you will assist in the conduct of Phase I studies within Pharmaceutical Services area in accordance with ICH Good Clinical Practice (GCP) and following local regulatory requirements and relevant Standard Operating Procedures (SOP's). You will assist and participate in the assembly /dispensing of Investigational Medicinal Product (