
Senior Scientific Researcher
2 weeks ago
We are seeking a highly skilled and experienced Clinical Research Associate to join our team. As a key member of our organization, you will be responsible for ensuring the conduct of studies is in compliance with regulatory requirements.
Key Responsibilities:
- Ensure that study protocols are adhered to
- Conduct on-site monitoring visits
- Review and input into study protocols, CRFs, and validation tools
- Prepare and review Monitoring Guidelines, CRF Completion Guidelines, and patient information documents
- Assist in submissions to ethics committees and competent authorities
- Manage investigator and institution contracts
- Collaborate with the Clinical Data Management Team
- Participate in feasibility studies and Investigator selection
Requirements:
- University degree in sciences or related fields
- At least 2 years experience as a Clinical Research Associate in a pharmaceutical company or CRO
- Strong knowledge of relevant guidelines (e.g. ICH GCP) and regulatory requirements
- Fluent English language skills
- Strong communication and organizational skills
- Travel availability
As a leading global CRO, we offer individualized solutions tailored to our clients' specific needs. Our teams work collaboratively, providing maximum transparency throughout each study. We prioritize quality, focusing on therapeutic areas such as oncology, immunology, and CNS based on our expertise and experience.
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