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
Comply with required training curriculum.
Complete timesheets accurately as required.
Submit expense reports as required.
Update CV as required.
Maintain a working knowledge of and comply with Parexel processes, ICH-GCPs and other applicable requirements.
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 among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com.
Community Guidelines
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