Clinical Research Investigator (MD/DO)

DM Clinical Research; Albuquerque (NM); On-site; USD 100,000 - 130,000; Full time

Job summary

A leading clinical research organization in Albuquerque, NM is seeking a Clinical Research Investigator (MD/DO) to conduct clinical trials while ensuring the safety and well-being of participants. The ideal candidate will have a medical license and at least 2 years of experience in clinical research. Responsibilities include managing trials, maintaining quality standards, and strategizing for patient recruitment. This role requires meticulous attention to detail and ethical conduct in all aspects of clinical research.

Qualifications

• Must hold a Medical License (MD or DO).
• Minimum of 2 years of experience as a Clinical Research Investigator.

Responsibilities

• Conduct clinical trials in accordance with ICH, GCP, local regulations, and study protocols.
• Ensure the medical well-being and safety of study participants.
• Assist in maintaining clinical oversight and quality on studies.

Skills

Clinical trial management

Patient recruitment strategies

Ethical conduct

Attention to detail

Education

Medical License (MD, DO)

Job description

Position:Clinical Research Investigator (MD/DO)

Location: Albuquerque, NM

Job Id:539

# 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 Albuquerque, NM . 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.