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Clinical Research Coordinator
2 months ago
Job Summary
Medix™ is seeking a highly skilled Clinical Research Coordinator to join our team. As a Clinical Research Coordinator, you will play a critical role in the success of our clinical trials by ensuring the smooth execution of study protocols and procedures.
Key Responsibilities
- Data Management
- Collect, enter, and maintain accurate and complete records for clinical study subjects.
- Support timely and accurate data entry in electronic databases.
- Study Coordination
- Ensure all protocol-required procedures and visits occur according to specified guidelines.
- Manage participant enrollment and ensure compliance with the protocol during participant recruitment, informed consent, participant education, eligibility assessment, participant care, and follow-up per protocol.
- Regulatory Compliance
- Collaborate with quality assurance (QA) in the development of source documentation for new studies.
- Assist in the assessment of toxicities/adverse events and reporting serious adverse events per IRB and sponsor requirements.
- Communication and Collaboration
- Possess excellent interpersonal skills and collaborate with the research team.
- Independently manage workflows and prioritize numerous tasks.
- Professional Development
- Maintain GCP certification and IATA training as required.
- Perform other duties as assigned.
Requirements
- Excellent communication and interpersonal skills.
- Ability to work independently and prioritize multiple tasks.
- Strong organizational and time management skills.
- Ability to maintain confidentiality and handle sensitive information.
- Proficiency in electronic data management systems.
What We Offer
- A dynamic and supportive work environment.
- Opportunities for professional growth and development.
- A competitive salary and benefits package.
