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 (

Die Parexel Early Phase Clinical Unit unterstutzt die Entwicklung innovativer neuer Medikamente, mit Fruhphasen und First in Human" Studien. Diese sind der erste Schritt zur Erprobung neuartigen Behandlungen am Menschen um deren Resultate zu verbessern. In der Parexel Berlin Unit (auf dem Gelande der DRK Kliniken Berlin Westend) sind unsere hochqualifizierten und erfahren

Design and develop systems and data integrations using MuleSoft Anypoint Platform. Design and develop high quality APIs and Integrations. Develops unit tests and provides code coverage to accurately testing business logic and functionality. Creates high level design documents, including MuleSoft functionality. Support and fine tune existing integration architecture and co

Using Microsoft Azure data PaaS services, design, build, modify, and support data pipelines leveraging DataBricks and PowerBI in a medallion architecture setting. If necessary, create prototypes to validate proposed ideas and solicit input from stakeholders. Excellent grasp of and expertise with test driven development and continuous integration processes. Analysis and De

Under departmental supervision, the Medical Writer will research, create, edit, and coordinate the production of PBRER/PSUR for submission to regulatory authorities. The Medical Writer would serve as the primary client contact. The Medical Writer must have minimum 3 years of experience in authoring or supporting PBRER/PSUR Key Accountabilities Accountability Supporting Ac

We are recruiting for an RWE Senior Associate based in either Sweden or Denmark. who will provide a broad range of consulting services and works within projectguidelines to identify, refine, and address client issues and to achieve project objectives for our RWE portfolio. The Consultant providesoverall project leadership and provides guidance to project team members on t