- Increase patient access to research trials within our communities,
- Provide physicians with enhanced care options for current patients, and
- Deliver superior clinical research enrollment metrics to Pharma sponsors.
- 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
- 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
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Clinical Research Site Director - Columbia, United States - ObjectiveHealth
Description
Clinical Research Site DirectorOur clinical research company is looking to hire a qualified candidate for the full-time position of Clinical Research Site Director. The ideal candidate will possess certification such as RNB, LPN, phlebotomy, or similar, prior clinical research experience, and have a strong desire to work directly with patients.
Who We Are
ObjectiveHealth is a clinical research company that uses proprietary technology to:
We want you to join us in doing just that.
Who You Are
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, and 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.
