Principal Investigator

Company Description

Andes Clinical Research, located in Orem, UT, is dedicated to serving and educating the community about available clinical trials. The company prioritizes inclusivity and delivers reliable data to empower better-informed decisions. Join Andes Clinical Research in their pursuit of excellence as they provide and collect data that represents everyone.

Role Description

This is a full-time on-site role for a Principal Investigator at Andes Clinical Research. The Principal Investigator will be responsible for leading and overseeing clinical research studies, including protocol development, participant recruitment, data collection, analysis, and reporting. The role involves working closely with research teams, sponsors, and regulatory authorities.

Key Responsibilities:

• Design, plan, and execute clinical trials in accordance with regulatory and ethical guidelines.
• Oversee all aspects of trial implementation, including protocol development, site selection, and subject recruitment.
• Ensure compliance with Good Clinical Practice (GCP) and applicable regulations.
• Collaborate with sponsors, regulatory agencies, and institutional review boards (IRBs).
• Monitor trial progress and conduct regular team meetings to address challenges.
• Analyze trial data and prepare reports for regulatory submissions and publications.
• Mentor and train clinical research staff and support personnel.
• Maintain accurate and up-to-date documentation and records.

Qualifications:

• MD, DO, or equivalent medical degree; General practitioner preferred. (Current ML in other states is a plus).
• Minimum of 1 year(s) of experience as a Principal Investigator in clinical trials.
• Strong knowledge of GCP, FDA regulations, and clinical trial methodology.
• Proven ability to manage multiple projects simultaneously and meet deadlines.
• Excellent communication and interpersonal skills.
• Strong analytical and problem-solving abilities.
• Commitment to patient safety and ethical conduct of research.