Clinical Research Site Director

ObjectiveHealth; Columbia Township (MO); On-site; USD 120,000 - 160,000; Full time

Benefits offered by this job

401(k) matching

Health Insurance

Dental Insurance

Vision Insurance

PTO

Adoption Assistance

Paid Holidays

Disability Insurance

HSA / FSA

Career progression

Job summary

ObjectiveHealth is hiring a Clinical Research Site Director to lead our clinical research sites and coordinate industry-sponsored trials. You will oversee patient care activities, ensure protocol compliance, and drive enrollment while maintaining data integrity and regulatory standards.

The role calls for strong leadership, clear communication with sponsors and monitors, and a commitment to our core values as we expand trials across multiple therapeutic areas.

Qualifications

• Experience conducting IRB-approved clinical trial protocols: identification, screening, randomization, enrollment and clinic visits.
• Skilled at performing and assisting with direct patient care activities: consenting patients, physical assessments, blood draws, medication administration, ECG.
• Attention to detail for clean data entry, regulatory compliance, site visits, study setup and protocol adherence.
• Excellent communicator to foster relationships between research team, PIs, Sponsors, Monitors and others.
• Advocate for Company values, mission and initiatives.
• Ability to stay focused while running protocols, resolving IRB responses and audit findings, tracking AE/SAE, maintaining eSource.
• Interest in advancing therapy development in Gastroenterology, Urology, Respiratory, Orthopedics, Dermatology and Oncology.

Responsibilities

• Taking ownership of assigned studies and patients.
• Communicating promptly and effectively with leadership and coworkers when questions arise.
• Showing up on time, every time.
• Ensuring strict compliance to laws, regulations and governing body requirements.
• Learning and using the technologies provided to enhance day-to-day activities.
• Embodying core values of Compassion, Integrity, Collaboration, Innovation, Velocity and Dedication.

Skills

Patient interaction

Leadership

IRB protocol

Data entry accuracy

Regulatory compliance

Communication

eSource management

Attention to detail

Tools

ECG

Job description

Description

Clinical Research Site Director

ObjectiveHealth is currently seeking a qualified candidate for the full-time position of Clinical Research Site Director. The ideal candidate will have prior experience in site leadership and 5 years of experience coordinating industry-sponsored clinical trials.

Who We Are

ObjectiveHealth is a clinical research company that uses proprietary technology to:

1. Increase patient access to research trials within our communities,
2. Provide physicians with enhanced care options for current patients, and
3. Deliver superior clinical research enrollment metrics to Pharma sponsors.

All with the goal of Improving Patient Outcomes at the point of care.

We want you to join us in doing just that.

Who You Are

• 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
• A proven leader among your peers and teams
• 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: 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
• Energized by the idea of playing a role in the future of new therapy development in the areas of Gastroenterology, Urology, Respiratory, Orthopedics, Dermatology, and/or Oncology

What Success Looks Like for This Role

• 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 enhance your day-to-day activities
• Embodying our core values of Compassion, Integrity, Collaboration, Innovation, Velocity, and Dedication

What We Offer

• 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
• a wide selection of other voluntary benefits

Requirements

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

ObjectiveHealth is an EEO Employer and an E-Verify participant.