Study Manager/CPM All Location

Benefits

Additional Information

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. CRA: Knowledge and Experience: - At least 1.5 years (2 years preferable) of Clinical Monitoring/ Site Management experience, global study monitoring experience is preferred - Good knowledge of ICH/GCP, relevant international and local regulations relating to Clinical Research Education: - Degree in Life Science, Pharmacy, or other relevant education background - Bachelor's degree or above, or equivalent Study Manager: Knowledge and Experience: - Minimum of BS/BA in a biomedical discipline or equivalent education/training is required. - At least 7 years in clinical practices. - Good working knowledge of Good Clinical Practices (GCPs), monitoring, clinical drug development process and country regulatory environment. - Experience with clinical research methodology (e.g., study design, study monitoring and data analysis). Prior study management and/or study coordination experience preferred. - Demonstrated effectiveness in working in a multidisciplinary, matrix team situation. - Advanced education and/or training/experience desirable. Education: - Degree in Life Science, Pharmacy, or other relevant education background - Bachelor's degree or above, or equivalent

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