Clinical Research Coordinator I
About the role
Our clinical research company is looking to hire a qualified candidate for the full-time position of Clinical Research Coordinator. The ideal candidate will possess certification such as an MA, phlebotomy, or similar and have a strong desire to work directly with patients.
ObjectiveHealth is a clinical research company that uses proprietary technology to: increase patient access to research trials within our communities, provide physicians with enhanced care options for current patients, and deliver superior clinical research enrollment metrics to Pharma sponsors — all with the goal of improving patient outcomes at the point of care.
Responsibilities
- Take ownership of assigned studies and patients
- Communicate promptly and effectively with leadership and coworkers when you have a question or see something that needs correction
- Show up on time, every time
- Ensure strict compliance with the laws, regulations, and requirements of all applicable governing bodies
- Learn and use the technologies provided to increase efficiency in day‑to‑day activities
- Embody the core values of Compassion, Integrity, Collaboration, Innovation, Velocity, and Dedication
- Identify, screen, randomize, and enroll patients
- Conduct clinic visits
- Consent patients
- Perform physical assessments, blood draws, medication administration, and ECG
- Assist with direct patient care activities
- Maintain acute attention to detail for clean data entry, regulatory compliance, productive site visits, efficient study set‑up and maintenance, and strict protocol adherence
- Foster relationships between the research team, PIs, sponsors, monitors, and others
- Advocate for company values, mission, and initiatives
- Stay focused while running different protocols, resolving and submitting IRB responses and audit findings, tracking AE and SAE events, and maintaining eSource material for assigned studies
- Be energized by the opportunity to contribute to future therapy development in gastroenterology, urology, dermatology, and/or oncology
Qualifications / Skills
- Certification such as MA, phlebotomy, or similar
- Lover of patient interaction and skilled at providing patient care
- Team player with a bias for action and an attitude that takes personal responsibility
- Skilled in all aspects required for conducting an IRB‑approved clinical trial protocol
- Skilled at performing and assisting with direct patient care activities
- Possess acute attention to detail for clean data entry, regulatory compliance, productive site visits, efficient study set‑up and maintenance, and strict protocol adherence
- Expert communicator with the goal of fostering relationships between the research team, PIs, sponsors, monitors, and others
- Strong advocate for company values, mission, and initiatives
- Not easily distracted: ability to stay focused while running different protocols, resolving and submitting IRB responses and audit findings, tracking AE and SAE events, and maintaining eSource material
- Energized by the idea of playing a role in the future of new therapy development in gastroenterology, urology, dermatology, and/or oncology
Benefits
Competitive compensation, 401(k) with Company match, a clear career pathway for advancement within the Company, Short‑ and Long‑Term Disability, Health Savings and Flexible Spending Accounts, Health, Dental and Vision insurance Plans, Generous PTO, Adoption Assistance, Paid Holidays, and a wide selection of other voluntary benefits.
Requirements
This job requires legal authorization to work in the US.