Clinical Research Investigator (MD/DO)

DM Clinical Research; Miami (FL); On-site; USD 100,000 - 150,000; Full time

Job summary

A leading clinical research organization in Miami, FL, is seeking a Clinical Research Investigator with an MD or DO degree. This role encompasses conducting clinical trials per protocols while ensuring participant safety and oversight. Responsibilities include conducting physical exams, reviewing lab results, and contributing to patient recruitment strategies. This position requires meticulous attention to detail and compliance with ICH and local regulations, making it ideal for professionals committed to high-quality clinical research.

Qualifications

• MD or DO degree required to practice medicine in the US.
• Experience in conducting clinical trials preferred.
• Familiarity with ICH, GCP, and local regulations.

Responsibilities

• Conduct physical exams per protocol.
• Ensure participant safety and well-being during trials.
• Review and assess lab abnormalities according to protocol.
• Maintain oversight and quality of clinical studies.
• Participate in strategies for patient recruitment.

Skills

Clinical trial management

Patient assessment

Regulatory compliance

Attention to detail

Education

MD or DO degree

Job description

Position: Clinical Research Investigator (MD/DO)

Location: Miami, FL

Job Id: 522

# of Openings: 0

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 an MD or DO for our clinical research site in Miami, FL to serve as a sub‑investigator on clinical research trials. This medical professional will conduct clinical trials (studies) according to ICH, GCP, local regulations, study protocols, and company processes.

Responsibilities

• Conduct physical exams per protocol
• Review labs and assess abnormalities for clinical significance per protocol
• 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.