Clinical Study Start-up Associate
Há 5 dias
Job Opportunities in Clinical Research Management
We are seeking a highly skilled individual to join our team as a Clinical Study Start-up Associate II. As a key member of our team, you will be responsible for preparing and submitting regulatory documents for clinical trials.
Key Responsibilities:- Preparation and submission of regulatory documents according to relevant requirements
- Collection and update of information on regulatory requirements for selected countries
- Bachelor's Degree or local equivalent from a Medical or Science background
- A minimum of 2 years of experience in clinical study start-up requirements and activities
- Fluency in the local language and English
At [Company Name], we offer a comprehensive total reward package that includes base pay, variable pay and recognition programs. Our best-in-class employee benefits, supportive policies and wellbeing initiatives are designed to support you and your family throughout your career.
We are an equal opportunity employer committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
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