Clinical Research Investigator (MD/DO)

DM Clinical Research; Tucson (AZ); On-site; USD 80,000 - 100,000; Full time

Job summary

A leading clinical research organization is seeking a Clinical Research Investigator (MD/DO) for its Tucson, AZ site. The role involves ensuring participant safety, maintaining clinical oversight, and conducting evaluations to comply with study protocols and regulations. Candidates must hold a valid medical license and have at least 2 years of experience as a Clinical Research Investigator. This position offers the opportunity to work on diverse clinical trials in a thriving research environment.

Qualifications

• Must hold a valid Medical License (MD, DO).
• At least 2 years of experience as a Clinical Research Investigator.

Responsibilities

• Ensure the safety and medical well-being of trial participants.
• Maintain clinical oversight and quality on registered studies.
• Review enrollment progress and participant retention rates.
• Interpret protocols and develop patient recruitment strategies.
• Conduct clinical evaluations to enroll eligible participants.
• Ensure compliance with ethical and safety standards.
• Pay attention to detail in documentation and patient care.

Skills

Clinical oversight

Patient recruitment strategies

Detailed documentation

Education

Medical License (MD, DO)

Job description

Position: Clinical Research Investigator (MD/DO)

Location: Tucson, AZ

Job Id:538

# of Openings:0

Clinical Research Investigator

DM Clinical Research, the largest privately-owned research management organization in the Houston area and one of the top 50 in the country, is looking for anInvestigatorfor our sites in the Tucson, AZ, area. This individual will conduct all clinical trials (studies) according to ICH, GCP, local regulations, study protocols, and company processes.

Responsibilities

• Ensures the medical well-being and safety of the participants through the safe performance and execution of the studies.
• Assists in maintaining clinical oversight and quality on the studies registered on and delivers on study targets, thereby contributing to the commercial success of the site.
• Reviews enrollment progress, pre-screening and screening success rates, screen failure rates, safety, and retention of participants.
• Interprets protocols and IB and participates in initiatives to strategize for patient recruitment.
• Carries out clinical evaluation and assessment of participants to ensure eligible participants are enrolled onto studies.
• Ensures and protects the welfare and safety of participants through ethical conduct.
• Fulfills and comply with all medical duties as per protocol, SOP/COP and ICH GCP and local regulations.
• Exercises meticulous attention to detail in documentation and patient care.

Requirements

• Medical License (MD, DO)
• At least 2 years of experience as a Clinical Research Investigator.