Senior Regulatory Affairs Associate-Clinical Trial Applications

Parexel is looking for a Senior Regulatory Affairs Associate-Clinical Trial Applications to support projects in Brazil! We are looking for an individual who has experience within clinical trial applications for beginning clinical trials and also with submissions to ethics committees.

The Senior Regulatory Affairs Associate must have an understanding of the organization’s basic consulting models and methodologies, as well as basic knowledge of what services R&A provides. They must be technically competent and continually developing their skills.

The Senior Associate, under the general direction of a Project Lead and/or Technical SME,

takes responsibility for ensuring that client work is performed, and delivered on time, meeting the quality expectations of R&A and the client. The Senior Associate may act in a client facing role with support from line management. When serving as a Project Lead or Work Stream Lead, they will assure the work of the entire team or work stream is delivered on time and that it meets client’s and PC’s quality expectations.

The candidate will also have:Project management knowledgeClient-focused approach to workResults orientationTeamwork and collaboration skillsExcellent interpersonal and intercultural communication skills, both written and verbalCritical thinking and problem-solving skillsProficiency in local language and extensive working knowledge of the English languageQualificationsExperience:2-3 years of Regulatory experience

Education:Bachelor's degree in a science field or other related field.