Clinical Research Investigator (MD/DO)

DM Clinical Research; Boston (MA); On-site; USD 120,000 - 180,000; Full time

Job summary

A leading clinical research organization in Boston, MA is seeking a Clinical Research Investigator (MD/DO) to oversee clinical trials. This position requires conducting studies per regulations, ensuring participant safety, and maintaining clinical quality. Candidates must hold a valid medical license in Boston and have a minimum of two years' experience. Bilingual in Spanish is a plus. The role offers flexible hours to accommodate scheduling needs.

Qualifications

• Must have a valid medical license to practice in Boston.
• Minimum of 2 years experience as a Clinical Research Investigator.
• Attention to detail in documentation and patient care is critical.

Responsibilities

• Ensure the medical well-being and safety of participants.
• Assist in maintaining clinical oversight and quality of studies.
• Review enrollment progress and participant retention.
• Interpret protocols and participate in patient recruitment strategies.
• Carry out clinical evaluations to ensure participant eligibility.
• Comply with all medical duties and regulations.

Skills

Clinical oversight

Patient recruitment strategies

Meticulous documentation

Bilingual Spanish

Education

Medical license (MD/DO)

Job description

Position:Clinical Research Investigator (MD/DO)

Location: Boston, MA

Job Id:1012

# of Openings:1

Clinical Research Investigator (MD/DO)

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 Investigator for our site in Boston, MA. 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 eligibility to enroll in studies.
• Ensures and protects the welfare and safety of participants through ethical conduct.
• Fulfills and complies 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) - Boston
• 2 years experience as a Clinical Research Investigator (Principal Investigator or Sub-Investigator)
• Bilingual Spanish a plus

Flexible hours - schedule can be tailored as required.