Parexel Biotech is dedicated to the biotech industry in supporting our customers with more efficient drug discovery strategies and our regulatory expertise and our support to guide them through an NDA and revenue perspective. We leverage our Subject Matter Experts early in the process to consult with customers to guide them on the right pathway. Our goal is to partner wit

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

Home Based, US The Quality Assurance (QA) Compliance Manager has a high level of knowledge and experience of appropriate GxP compliance and other applicable regulations and laws, Parexel procedures and appropriate Parexel processes to conduct audits and provide expert advice to internal and external clients. To effectively lead, matrix manages, develop, and implement assi

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Works with Precision Medicine Strategy Lead as well as clinical study teams to ensure quality samples and data are delivered to support biomarker evaluation and delivery of science to medicine. Responsibilities include oversight of clinical sample collection, usage per informed consent form, sample tracking (chain of custody) and sample destruction. Individual will work c

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

The Project Leadership function at Parexel is a critical part of driving success for our clients and advancing clinical research projects. As a part of the Global Project Leadership organization, your work has a direct impact on the projects, teams, and clients you work with, while helping deliver projects to the benefit of the patients we serve. Parexel's defined Biotech

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

Parexel's Strategic CGMP Compliance team is known for our unparalleled breadth and depth of expertise globally. Parexel CGMP Compliance offers services which create and maximize product value for clients throughout the product lifecycle, leveraging our unique fusion of scientific, regulatory, and business expertise. We are the pre eminent regulatory and GxP (Good Clinical

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

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. The Senior IT Disaster Recovery (DR) Project Manager will be responsible for managing the activities to ensure that Parexel is able to recover our IT systems in the ev

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

Parexel has an exciting opportunity for a strategic individual with RWE clinical study design and delivery experience to fill our Associate Director / Director, Integrated Solutions Real World Evidence & Market Access position. The person selected for this position will work directly with both clients and internal teams to find solutions and strategies to direct creative

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

The HR Associate acts as a first point of contact and support for managers and employees who require HR assistance with using or accessing HR programs and processes. The Associate is responsible for providing a timely and accurate response or properly redirecting the inquiry, to help the employee resolve or address their need. May serve as an SME or SPOC for a HR program,