Clinical Research Site Director

ObjectiveHealth • Columbia, MO

2d

About The Position

ObjectiveHealth is seeking a full-time Clinical Research Site Director with prior site leadership experience and five years of experience coordinating industry-sponsored clinical trials. The role involves leading clinical research site activities and assigned studies, supporting patient care and interaction, and ensuring studies are conducted in strict compliance with approved protocols and applicable requirements. The position may involve research in Gastroenterology, Urology, Respiratory, Orthopedics, Dermatology, and/or Oncology.

Requirements

• Prior experience in site leadership.
• Five years of experience coordinating industry-sponsored clinical trials.
• Legal authorization to work in the United States; work visas are not currently accepted.
• Ability to conduct or support clinical trial activities, including patient identification, screening, randomization, enrollment, and clinic visits.
• Ability to perform or assist with patient care activities such as consenting patients, physical assessments, blood draws, medication administration, and ECGs.
• Strong attention to detail, including for data entry, regulatory compliance, study setup and maintenance, and protocol adherence.
• Strong communication and relationship-building skills.
• Ability to manage multiple protocols and related study responsibilities while maintaining focus.

Responsibilities

• Lead assigned clinical research studies and take ownership of study participants.
• Conduct the activities required for IRB-approved clinical trial protocols, including patient identification, screening, randomization, enrollment, and clinic visits.
• Perform or assist with direct patient care activities, including informed consent, physical assessments, blood draws, medication administration, and ECGs.
• Maintain accurate data entry, regulatory compliance, protocol adherence, study setup and maintenance, and productive site visits.
• Resolve and submit IRB responses and audit findings, track adverse events and serious adverse events, and maintain eSource materials for assigned studies.
• Communicate promptly and effectively with leadership and coworkers about questions or issues requiring correction.
• Learn and use company-provided technologies to support day-to-day activities.
• Foster working relationships among the research team, principal investigators, sponsors, monitors, and others.

Benefits

• Competitive compensation
• 401(k) with Company match
• Career pathway for advancement within the Company
• Short- and Long-Term Disability
• Health Savings and Flexible Spending Accounts
• Health insurance
• Dental insurance
• Vision insurance
• Generous paid time off
• Adoption Assistance
• Paid Holidays
• Other voluntary benefits

What This Job Offers

• Job Type: Full-time
• Career Level: Manager
• Education Level: No Education Listed