Senior Research Professional
Há 2 dias
Role Overview:
">As a Clinical Research Associate, you will be part of a dynamic team that works on large-scale clinical studies.
">- ">
- Set up and monitor clinical studies to ensure high-quality data and compliance with regulations">
- Coordinate with stakeholders to identify and select investigational sites for clinical studies in phases II - IV">
- Prepare and review study documentation, including feasibility studies and regulatory submissions">
- Work independently to balance multiple tasks and prioritize responsibilities effectively">
- Collaborate with colleagues to achieve project goals and objectives">
- Maintain accurate records and reports, ensuring adherence to applicable regulations and principles of ICH-GCP">
Required Skills and Qualifications:
">- ">
- Advanced English skills with ability to read, write, and speak fluently">
- Vaccine or oncology experience">
- Excellent communication and interpersonal skills">
- Ability to work independently and collaboratively as part of a team">
- Strong organizational and time management skills">
- Proficiency in using technology to facilitate productivity and efficiency">
Benefits:
">- ">
- Opportunity to work on high-impact clinical studies">
- Collaborative and dynamic work environment">
- Professional growth and development opportunities">
- Competitive compensation and benefits package">
Others:
">This role offers the chance to make a meaningful contribution to the field of clinical research while developing your skills and expertise.
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