Clinical Research Coordinator I

ObjectiveHealth is a clinical research company that uses proprietary technology to improve patient access to research trials, provide physicians with enhanced care options, and deliver superior clinical research enrollment metrics. The Clinical Research Coordinator I will conduct IRB-approved clinical trial activities, provide direct patient care, maintain regulatory compliance, and coordinate with research stakeholders across assigned studies.

Responsibilities

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

Not easily distracted: You have the 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

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

Benefits

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

A wide selection of other voluntary benefits

Company

Integrated clinical research services for physician practices and healthcare organizations.

Franklin, Tennessee, USA

https://objective.health/

Founded in 2018

201-500 employees

Qualifications

The ideal candidate will possess certification such as an MA, phlebotomy, or similar

A lover of patient interaction and skilled at providing patient care

A 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: 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

Not easily distracted: You have the 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

This job requires legal authorization to work in the US. We are not currently accepting work visas

Required skills

Clinical Trial Coordination, Phlebotomy, Medical Assistant Certification, Patient Care, Informed Consent, Physical Assessments, Blood Draws, Medication Administration, ECG, IRB Compliance, Adverse Event Tracking, eSource

Experience

Entry level