Clinical Research Associate
4 weeks ago
As a Clinical Research Associate at Pharmiweb, you will be responsible for monitoring the progress of clinical studies at investigative sites or remotely. Your primary goal will be to ensure that clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.
Key Responsibilities
- Monitor Phase I Oncology studies
- Ensure compliance with ICH and local regulatory authority regulations regarding drug
- Collaborate with cross-functional teams to achieve project goals
Requirements
- B.A./B.S. with strong emphasis in science and/or biology preferred
- 2+ years of clinical monitoring experience required
- Knowledge of ICH and local regulatory authority regulations regarding drug
- Oncology experience required
- Phase 1 experience preferred
What We Offer
- Competitive salary and benefits package
- Opportunities for professional growth and development
- Collaborative and dynamic work environment
About Us
Pharmiweb is a leading provider of clinical research services. We are committed to delivering high-quality results and exceptional customer service. Our team is passionate about making a difference in the lives of patients and families affected by cancer.
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