At a glanceSummarised by Seekless from the posting.
Must have11
Build and maintain engagement with Investigators, other site staff
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
Previous experience in scientific and/or regulatory medical writing
Strong Communication Skills
Keen problem-solving skills
Fluent in both oral and written English
Fluent in host country language
At least 5 years in clinical practices
Minimum of BS/BA in a biomedical discipline or equivalent education/training
Eligibility5
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
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
Hiring process
• 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