Clinical Research Coordinator I: Patient-Centric Trials

ObjectiveHealth; Laurel (MD); On-site; USD 50,000 - 75,000; Full time

Benefits offered by this job

Competitive compensation

401(k) with company match

Paid holidays

PTO

Health, dental & vision insurance

Disability insurance

HSA/FSA

Adoption assistance

Career advancement pathway

On-site work

Job summary

ObjectiveHealth in Laurel, MD is seeking a Clinical Research Coordinator I to manage patient-facing activities within IRB-approved studies. You will identify, screen, enroll patients, conduct clinic visits, and perform consent and basic assessments.

The role requires strong data entry accuracy, regulatory compliance, and clear communication with investigators, sponsors, and monitors. This position offers full-time hours and a dedicated team focused on advancing therapy development.

Qualifications

• Certification as MA or phlebotomy preferred.
• Experience in IRB-approved clinical trials.
• Direct patient care and consent experience.
• Excellent data entry and regulatory compliance.

Responsibilities

• Identify, screen, randomize, and enroll patients per protocol.
• Conduct clinic visits and direct patient care activities.
• Obtain informed consent and perform assessments.
• Ensure data accuracy and regulatory documentation.

Skills

Patient interaction

Teamwork

Regulatory compliance

Data entry accuracy

Study protocol execution

Communication with team

Education

Medical Assistant (MA) certification

Phlebotomy certification

Job description

ObjectiveHealth in Laurel, MD is seeking a Clinical Research Coordinator I to manage patient-facing activities within IRB-approved studies. You will identify, screen, enroll patients, conduct clinic visits, and perform consent and basic assessments.

The role requires strong data entry accuracy, regulatory compliance, and clear communication with investigators, sponsors, and monitors. This position offers full-time hours and a dedicated team focused on advancing therapy development.