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

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

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

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

Written and oral fluency in English Knowledge and Experience Demonstrates technical aptitude with awareness/potential prior experience in Microsoft Office Products (basic computer skills). Basic understanding of data management processes and data validation flow (e.g. Data cleaning, DB lock) Basic understanding of relevant ICH GCP Guidelines, local regulatory requirements

We are currently looking for a part time Receptionist (30 hours/week) to be based in our office in Prague. In this role you will Handle all telephone calls in a professional and efficient manner Develop effective relationships with internal client General administrative functions (filing, printing, copying, faxing, laminating etc) Greet visitors (clients/vendors) with a p

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Parexelstrives to be the premier provider to the biopharmaceutical and medical device industries for the development and commercialization of new medical therapies worldwide. Our mission is to combine the strength of our expertise, experience and innovation to advance the worldwide success of the biopharmaceutical and medical device industries in preventing and curing dis

An exciting opportunity for Laboratory Assistant (bank) to join the Early Phase team based at Parexel's Clinical Unit in Harrow (located in Northwick Park hospital). Do you have practical laboratory experience in the pharmaceutical industry and/or research institute? Are you practical and dexterous? Then we would like to hear from you! As a Laboratory Assistant you will c

of the Role The Senior Statistical Programmer provides technical expertise for the conduct of clinical trials, acts as an internal subject matter expert in specific areas providing technical support and expert advice, and works independently to support various programing activities related to the analysis and reporting of clinical study data. In addition, the Senior Statis

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