Clinical Research Coordinator I

ObjectiveHealth • Folsom, CA

8d

About The Position

ObjectiveHealth is hiring a full-time Clinical Research Coordinator to work directly with patients and support clinical research studies. The role involves coordinating assigned studies and patients, conducting clinical trial activities in accordance with approved protocols, providing and assisting with direct patient care, maintaining study documentation and data, and ensuring regulatory compliance. The position supports research in areas including gastroenterology, urology, dermatology, and/or oncology. The ideal candidate has a relevant certification, such as medical assistant or phlebotomy, and a strong interest in patient interaction.

Requirements

• Legal authorization to work in the United States; work visas are not currently accepted.
• A certification such as medical assistant, phlebotomy, or similar is desired.
• Strong interest in direct patient interaction and patient care.
• Ability to conduct or support the clinical trial activities described, including patient screening and enrollment, clinic visits, consent, physical assessments, blood draws, medication administration, and ECGs.
• Attention to detail for data entry, regulatory compliance, study documentation, and protocol adherence.
• Strong communication and relationship-building skills.
• Ability to stay focused while managing multiple protocols and related study tasks.
• Punctuality, personal responsibility, teamwork, and a bias for action.

Nice To Haves

• Interest in clinical research and new therapy development in gastroenterology, urology, dermatology, and/or oncology.

Responsibilities

• Identify, screen, randomize, and enroll patients in IRB-approved clinical trials.
• Conduct clinic visits and perform or assist with patient care activities, including obtaining consent, physical assessments, blood draws, medication administration, and ECGs.
• Maintain accurate data entry, regulatory compliance, study setup and maintenance, and adherence to study protocols.
• Manage multiple protocols, IRB responses, audit findings, adverse event and serious adverse event tracking, and eSource materials for assigned studies.
• Take ownership of assigned studies and patients, and communicate promptly with leadership and coworkers about questions or needed corrections.
• Learn and use company-provided technologies to improve efficiency.
• Build effective working relationships with the research team, principal investigators, sponsors, monitors, and other stakeholders.
• Follow applicable laws, regulations, and requirements of governing bodies.

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