Clinical Research Coordinator I

ObjectiveHealth•Akron, OH

1d•Onsite

About The Position

ObjectiveHealth is a clinical research company that uses proprietary technology to increase patient access to research trials within 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. The company is looking to hire a qualified candidate for the full-time position of Clinical Research Coordinator I. The ideal candidate will love patient interaction, be skilled at providing patient care, and be a team player with a bias for action and personal responsibility. They should be skilled in all aspects required for conducting an IRB approved clinical trial protocol, including identification, screening, randomization, and enrollment of patients, and conducting clinic visits. The role also involves performing and assisting with direct patient care activities such as consenting patients, physical assessments, blood draws, medication administration, and ECG. Acute attention to detail for clean data entry, regulatory compliance, productive site visits, efficient study set-up and maintenance, and strict protocol adherence is essential. The coordinator will also be an expert communicator, fostering relationships between the research team, PIs, Sponsors, Monitors, and others, and a strong advocate for Company values, mission, and initiatives. They must be able to stay focused while managing different protocols, resolving and submitting IRB responses and audit findings, tracking AE and SAE events, and maintaining eSource material for assigned studies. The role is energized by the idea of playing a role in the future of new therapy development in Gastroenterology, Urology, Dermatology, and/or Oncology.

Requirements

Certification such as an MA, phlebotomy, or similar
Legal authorization to work in the US
Strong desire to work directly with patients
Skilled in all aspects required for conducting an IRB approved clinical trial protocol: identification, screening, randomization, and enrollment of patients, conducting clinic visits, etc.
Skilled at performing and assisting with direct patient care activities: consenting patients, physical assessments, blood draws, medication administration, ECG, etc.
Possess an acute attention to detail for clean data entry, regulatory compliance, productive site visits, efficient study set-up and maintenance, and strict protocol adherence
An expert communicator with the goal of fostering relationships between the research team, PIs, Sponsors, Monitors, and others
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 for assigned studies

Responsibilities

Identification, screening, randomization, and enrollment of patients for IRB approved clinical trial protocols
Conducting clinic visits
Performing and assisting with direct patient care activities: consenting patients, physical assessments, blood draws, medication administration, ECG
Ensuring clean data entry
Ensuring regulatory compliance
Conducting productive site visits
Ensuring efficient study set-up and maintenance
Ensuring strict protocol adherence
Fostering relationships between the research team, PIs, Sponsors, Monitors, and others
Advocating for Company values, mission, and initiatives
Running different protocols
Resolving and submitting IRB responses and audit findings
Tracking AE and SAE events
Maintaining eSource material for assigned studies
Taking ownership of assigned studies and patients
Communicating promptly and effectively with leadership and coworkers when questions or corrections are needed
Showing up on time, every time
Ensuring strict compliance to the laws, regulations, and requirements of all applicable governing bodies
Learning and using the technologies provided to increase efficiency in day-to-day activities
Embodying core values of Compassion, Integrity, Collaboration, Innovation, Velocity, and Dedication