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

Support of high throughput, pre formulation, pre qualification, robustness, or admixture testing Results processing and documentation by following appropriate methods / protocols / procedures Sample management and monitoring of controlled temperature units Following all appropriate laboratory safety and hygiene procedures Qualifications BS (5+ yrs . ) o f relevant experie

FSP (Function Service Provision)CROCRO CRA 1

What you'll do Leverage your expertise. Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV) and termination visits (TV) at assigned clinical sites and generate visit/contact reports. Build relationships. Oversee integrity of the study and utilize problem solving skills to promote rapport with the site and staff. Protect patients. Review

CRA (iCRA) CRA( ) CRA iCRA / (CRA)ICF CTMS, e TMF ,SOP, ,SOP, iCRAiCRA (CRA)5() TOEIC 700Reading & Writing

Local submission of CTA according to the EU directive until the end of the transition period in Belgium, France, Luxembourg and Monaco, then submission according to EU CTR Local submission of MAP and NIS Education Minimum of a Bachelor's Degree in a Scientific or Technical Discipline, Advanced Degree Preferred Language skills Must be fluent in French and Englishcommunicat

Provide a range of leadership and influencing capabilities to achieve the business objectives and goals for both Parexel and clients Effectively communicate with internal and external customers as well as third party vendors Participate in cross functional meetings and support initiatives to ensure the delivery of milestones and timelines for clinical trials Ensure all sy

The Director is expected to act as an Account Lead for a key client, group of clients, and/or a specific area of business to provide leadership, excellence in management, and expertise to support all aspects of Data Management projects within an account. The Account Lead provides general oversight, consistency in approach and leadership across an account where an account

Due to a growing portfolio, we are currently looking for an Enterprise Analytics & Intelligence Specialist to be based in South Africa with flexible working hours. Your time here As an Enterprise Analytics & Intelligence Specialist and Power BI / Spotfire expert, contribute to the implementation of the Business Intelligence infrastructure at Parexel. Key Accountabilities

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

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

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

Parexel Early Phase Clinical Unit supports the development of innovative new medicines which are vital for public health, improving outcomes, and saving lives. The early phase and "first in human" trials are the first step in testing these novel treatments in humans. At Parexel Glendale Unit the Nurse Manager will manage and assist our highly trained and skilled nurses. T

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

Are you currently a Physician Associate ? Are interested in pursuing a career in the Pharmaceutical Industry? We have an exciting opportunity for a Physician Associate the primary responsibility will be providing support to the Screening Department for human volunteer studies of new and existing pharmaceuticals performed in our Early Phase Clinical Unit (EPCU) in Harrow.