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ObjectiveHealth · 1 month ago

Clinical Research Coordinator II

St Louis, MO

Full-time

Onsite

Mid Level

3+ years exp

ObjectiveHealth is a clinical research company focused on improving patient outcomes through innovative technology. They are seeking a Clinical Research Coordinator II who will be responsible for managing clinical trials, ensuring compliance with protocols, and providing direct patient care.

Health CareMedicalMedical Device

No H1B

Responsibilities

Taking ownership of assigned studies and patients

Communicating promptly and effectively with leadership and coworkers when you have a question or see something that needs correction

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 we provide to increase efficiency in your day-to-day activities

Embodying our core values of Compassion, Integrity, Collaboration, Innovation, Velocity, and Dedication

Qualification

Clinical research coordinationPatient careIRB protocol complianceData entryCommunication skills

Required

3+ years of clinical research coordination experience

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

A 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 for assigned studies

Energized by the idea of playing a role in the future of new therapy development in the areas of Gastroenterology, Urology, Dermatology, and/or Oncology

Legal authorization to work in the US