Clinical Research Coordinator I

ObjectiveHealth • Laurel, MD

13h

About The Position

ObjectiveHealth is hiring a full-time Clinical Research Coordinator to support clinical research trials and provide direct patient care. The coordinator conducts assigned studies and clinic visits, supports patient identification, screening, randomization, and enrollment, and helps ensure study activities comply with approved protocols and applicable requirements. The role involves working across studies in areas such as gastroenterology, urology, dermatology, and/or oncology, while using company-provided technologies to improve daily efficiency.

The successful candidate takes ownership of assigned studies and patients, communicates effectively with colleagues and leadership, and maintains careful attention to patient care, data quality, regulatory compliance, and protocol adherence. The position collaborates with research teams, principal investigators, sponsors, monitors, and others.

ObjectiveHealth is a clinical research company that uses proprietary technology to increase community access to research trials, provide physicians with enhanced care options for existing patients, and deliver clinical research enrollment metrics to pharmaceutical sponsors, with the goal of improving patient outcomes at the point of care. The company offers competitive compensation and a benefits package, along with a career pathway for advancement.

Requirements

• Legal authorization to work in the United States; the company is not currently accepting work visas.
• Strong desire to work directly with patients.
• Ability to provide patient care and perform or assist with the listed clinical trial and direct patient care activities.
• Attention to detail in data entry, regulatory compliance, study setup and maintenance, and protocol adherence.
• Strong communication and relationship-building skills.
• Ability to stay focused while managing multiple protocols and related study tasks.
• Personal responsibility, a bias for action, teamwork, and punctuality.

Nice To Haves

• Certification such as medical assistant (MA), phlebotomy, or similar.
• Experience or interest in clinical research in gastroenterology, urology, dermatology, and/or oncology.

Responsibilities

• Conduct activities required for IRB-approved clinical trial protocols, including patient identification, screening, randomization, and enrollment.
• Conduct clinic visits and perform or assist with direct patient care, including patient consent, physical assessments, blood draws, medication administration, and ECGs.
• Take ownership of assigned studies and patients.
• Maintain accurate data entry, regulatory compliance, productive site visits, efficient study setup and maintenance, and strict protocol adherence.
• Manage multiple protocols, IRB responses, audit findings, adverse event and serious adverse event tracking, and eSource materials for assigned studies.
• Communicate promptly and effectively with leadership and coworkers, including raising questions or identifying needed corrections.
• Learn and use company-provided technologies to increase efficiency.
• Work collaboratively with the research team, principal investigators, sponsors, monitors, and others.

Benefits

• Competitive compensation
• 401(k) with company match
• Career pathway for advancement within the company
• Short- and long-term disability
• Health savings and flexible spending accounts
• Health insurance
• Dental insurance
• Vision insurance
• Generous paid time off
• Adoption assistance
• Paid holidays
• Other voluntary benefits

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: No Education Listed