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

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Our Senior IT Support representative is responsible for all support queries across the Data & Technology departments, working with a variety of users to resolve their technical issues in a prompt and efficient manner, whilst maintaining a positive customer experience as well as providing guidance and assistance to members of the site services team. Key Accountabilities Ac

Regulatory Affairs Consultant must have an understanding of the organization's consulting models and methodologies, as well as good knowledge of what services PC provides. The Consultant must have strong technical skills and may be developing specialist knowledge of a particular subject and/ or market. This key role in the organization ensures the timely performance of wo

We are recruiting for experienced Regulatory Affairs Professionals on various levels. In this role, you will focus on clinical trial submissions. We are looking for someone who is experienced in CTA, EU CTR knowledge and experience would be a strong plus. The role can be based in our office in Madrid or remote. Key Deliverables in the role Manage the local submissions (as

Deliver/Lead specific Systematic Literature Review project steps e.g. screening, extraction, protocol design, quantitative feasibility. Understands project specific requirements to customize deliverables per specifics and apply innovative evidence presentation strategies. Develops project deliverables as required in a typical Systematic Literature Review project e.g., sys

Deliver/Lead specific Systematic Literature Review project steps e.g. screening, extraction, protocol design, quantitative feasibility. Understands project specific requirements to customize deliverables per specifics and apply innovative evidence presentation strategies. Develops project deliverables as required in a typical Systematic Literature Review project e.g., sys