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Clinical Research Principal Investigator
4 weeks ago
Catalina Research Institute (CRI) is seeking a Clinical Research Principal Investigator to join their team in Montclair, CA. As a key member of the research team, you will be responsible for protecting human subjects and their rights during the conduct of clinical trials.
Key Responsibilities:
- Attend site initiation visits and training in-service for all current protocols.
- Maintain current licensure and complete required SOP training.
- Oversee and provide guidance to the clinical team, ensuring delegated duties are performed within protocol, GCP, and federal regulated standards.
- Ensure the integrity and validity of data obtained during clinical trials.
- Assist in training of support staff for all clinical trials.
- Recruit patients for clinical trials and refer to other site trials as necessary.
- Set schedules to accommodate patients onsite and/or offsite, including weekends and holidays.
- Conduct informed consent processes, evaluate patient eligibility, and collect medical and surgical history.
- Document source documents, lab results, and adverse events.
- Review and sign CRFs, electronic CRFs, and data clarification forms.
- Participate in monthly staff meetings and annual SOP meetings.
Requirements:
- MD: Doctor of Medicine with a minimum of 3 years' experience in clinical research.
- Fluency in Spanish and English.
- Excellent communication, problem-solving, and organizational skills.
- In-depth knowledge of FDA-GCP regulations and company SOPs.
About ACRS
American Clinical Research Services (ACRS) Holdings is dedicated to improving the quality of life for millions of Americans through scientific research. We are committed to providing equal employment opportunities to all employees and applicants for employment, and we prohibit discrimination and harassment of any type.
