
Research Study Coordinator
4 days ago
Clinical research is a cornerstone of innovation, driving breakthroughs in healthcare and medical advancements.
We offer tailored solutions that cater to the unique needs of our clients, focusing on transparency and quality throughout each study. Our expertise lies in therapeutic areas such as oncology, immunology, and CNS.
Key Responsibilities:
- Ensure compliance with approved study protocols, ICH GCP, SOPs, and regulatory requirements.
- Conduct on-site monitoring visits and review study protocols, CRFs, and validation tools.
- Prepare submissions to Ethics Committees and Competent Authorities.
- Negotiate arrangements for site payments and manage queries in cooperation with the Clinical Data Management Team.
- Assist sites and the study team in managing contacts with external service providers.
- Participate in feasibility studies and Investigator selection.
Requirements:
- University degree in sciences or related fields, with experience and knowledge of clinical trials and regulations.
- At least 2 years of experience as a Clinical Research Associate in a pharmaceutical company or CRO.
- Strong knowledge of relevant guidelines and regulatory requirements.
- Fluent English communication skills.
- Excellent team player with strong organizational skills and travel availability.
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