Clinical Study Start Up Associate
hace 3 semanas
At ICON, we're committed to advancing and improving patients' lives through innovative clinical research solutions. As a Study Start Up Associate, you'll play a critical role in ensuring the success of our clinical trials.
Key Responsibilities:
- Perform feasibility and site identification to ensure the smooth start-up of clinical trials.
- Negotiate site contracts and provide country-specific expertise to Study Start Up team leads and project teams.
- Prepare and coordinate submissions to regulatory, ethics, and other bodies.
- Develop, finalize, and review Master and Country Specific Subject Information Sheets/Informed Consent Forms.
Requirements:
- High school diploma or local equivalent.
- Bachelor's Degree in Life Sciences preferred.
- Minimum 1 year's experience or understanding of clinical study start-up requirements and activities.
- Experience in Clinical Trial operations and meeting regulatory guidelines.
- Proficient project management skills.
Why Join ICON?
We're committed to developing our employees in a continuous learning culture, where every experience adds to your professional development. Our comprehensive and competitive total reward package includes base pay, variable pay, and recognition programs, as well as best-in-class employee benefits, supportive policies, and wellbeing initiatives.
ICON is an equal opportunity and inclusive 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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