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- Serve as the principal investigator for clinical trials conducted within our site network.
- Design and develop research protocols, ensuring compliance with regulatory requirements and industry standards.
- Lead the screening of eligible participants for clinical trials.
- Collaborate with cross-functional teams, including research coordinators, data managers, and regulatory affairs, to ensure seamless trial execution.
- Conduct thorough and accurate assessments of study participants, adhering to protocol guidelines.
- Maintain up-to-date knowledge of relevant therapeutic areas and research methodologies.
- Ensure the safety and well-being of study participants throughout the trial duration.
- Collaborate with sponsors, contract research organizations (CROs), and other stakeholders to achieve study objectives.
- Medical Doctor (MD) or Doctor of Osteopathic Medicine (DO) degree.
- Board certification or eligibility in a relevant medical specialty.
- Previous experience as a Principal Investigator not required but preferred
Clinical Research Physician - Houston, United States - Medix
Description
THIS ROLE IS FULL-TIME
Ensure you read the information regarding this opportunity thoroughly before making an application.
We are seeking a qualified and motivated physician interested to work as a Clinical Research Principal Investigator and join our dynamic team. As a key member of our clinical research site network, the Principal Investigator will play a crucial role in leading and overseeing clinical trials, ensuring the highest standards of research conduct and ethical practices.
Responsibilities:
Qualifications: