Bilingual Clinical Research Coordinator I

ObjectiveGI, Inc.; Laurel (MD); Hybrid; USD 55,000 - 75,000; Full time

Benefits offered by this job

401(k) with Company match

Health, Dental and Vision insurance

Paid Time Off (PTO)

Disability insurance

HSA/FSA

Holidays

Job summary

ObjectiveHealth is seeking a Clinical Research Coordinator I - Bilingual (Spanish) to join our Maryland team in Laurel. The role emphasizes direct patient care, consent, and enrollment within IRB-approved protocols, with a focus on accurate data capture and regulatory compliance.

Ideal candidates will be fluent in Spanish, comfortable with clinical visits, and capable of coordinating screening, randomization, and ongoing study activities while maintaining strong communication with the research

Qualifications

• Eligible to work in the United States without visa sponsorship.
• Experience assisting with IRB-approved clinical trials and patient enrollment.
• Experience performing patient assessments and coordinating study visits.

Responsibilities

• Coordinate patient screening, enrollment, randomization, and visits.
• Obtain informed consent and perform basic clinical assessments.
• Conduct blood draws, ECGs, and medication administration as required.
• Maintain accurate regulatory documentation and data entry for each study.
• Track adverse events and ensure protocol adherence across sites.

Skills

Patient interaction

Team collaboration

IRB protocol execution

Direct patient care

Regulatory compliance

Data integrity/entry

Communication skills

Attention to detail

Education

MA certification

Phlebotomy certification

Tools

eSource systems

Job description

ObjectiveHealth is seeking a Clinical Research Coordinator I - Bilingual (Spanish) to join our Maryland team in Laurel. The role emphasizes direct patient care, consent, and enrollment within IRB-approved protocols, with a focus on accurate data capture and regulatory compliance.

Ideal candidates will be fluent in Spanish, comfortable with clinical visits, and capable of coordinating screening, randomization, and ongoing study activities while maintaining strong communication with the research