When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Key Accountabilities: General Accountabilities Build and maintain engagement with Investigators, other site staff in collaboration with other functions, to ensure trial speed and effective start up, conduct and close out. Ability to manage studies and processes to agreed quality and timelines. Ability to proactively identify & mitigate risks around study/site level in study execution. Knowledge of the clinical development process, understand concepts and principles of study design, and application to manage and run studies. Compliance with Parexel standards Complies with required training curriculum. Completes timesheets accurately as required. Submits expense reports as required. Updates CV as required . Maintains a working knowledge of and complies with Parexel processes, ICH- GCPs and other applicable requirements. Skills: Previous experience in scientific and/or regulatory medical writing. Strong Communication Skills. Knowledge and Experience: Keen problem-solving skills. Fluent in both oral and written English. Fluent in host country language required. At least 5 years in clinical practices. Education: Minimum of BS/BA in a biomedical discipline or equivalent education/training is required. Parexel is a leading global clinical research organization (CRO) providing insights-driven Clinical and Consulting solutions to the world’s life sciences industry. Leveraging deep local knowledge and a global breadth of clinical, regulatory and therapeutic expertise, our professionals worldwide work in partnership with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind — broadening access and making clinical research a care option for anyone, anywhere. Our proven track record spans 40+ years and drives us forward, advancing clinical research in healthcare’s most complex areas while harnessing innovation to drive efficiencies across every phase of the clinical development process. Our insights-driven approach, proven delivery and trusted execution are accelerating the delivery of life-changing treatments to patients — With Heart.™

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