Clinical Trials Coordinator
2 weeks ago
Apsida Life Science is collaborating with a prominent Contract Research Organization (CRO) seeking a Clinical Trials Coordinator.
Key Responsibilities:
- Manage all aspects of clinical trials, ensuring adherence to study protocols, industry standards, and regulatory requirements.
- Facilitate essential tasks such as initiating studies, managing vendors, recruiting participants, documenting data, and overseeing adverse event reporting.
- Provide training and support to team members regarding trial execution, protocol compliance, and effective communication.
- Ensure meticulous record-keeping and documentation practices are upheld.
- Communicate efficiently with colleagues, management, participants, sponsors, and service providers.
Qualifications:
- A Bachelor’s degree with a minimum of 2 years of experience in the life sciences field.
- Certification in Good Clinical Practice (GCP).
- Proficiency in conducting vital sign assessments, EKGs, blood collection, and laboratory specimen handling.
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