Clinical Research Coordinator I

ObjectiveHealth • Wichita Falls, TX

7h • Onsite

About The Position

ObjectiveHealth is a clinical research company that uses proprietary technology to 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. All with the goal of Improving Patient Outcomes at the Point of Care. We are seeking a qualified candidate for the full-time position of Clinical Research Coordinator I. The ideal candidate will have a background in patient care and a strong interest in developing the skills needed to coordinate and manage clinical trials.

Requirements

• Background in patient care
• Strong interest in developing the skills needed to coordinate and manage clinical trials
• Skilled in all aspects required for conducting an IRB approved clinical trial protocol
• Skilled at performing and assisting with direct patient care activities
• Legal authorization to work in the US

Nice To Haves

• 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
• 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, Dermatology, and/or Oncology

Responsibilities

• Identification, screening, randomization, and enrollment of patients
• Conducting clinic visits
• Performing and assisting with direct patient care activities: consenting patients, physical assessments, blood draws, medication administration, ECG, etc.
• Acute attention to detail for clean data entry, regulatory compliance, productive site visits, efficient study set-up and maintenance, and strict protocol adherence
• Fostering relationships between the research team, PIs, Sponsors, Monitors, and others
• Staying 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
• Playing a role in the future of new therapy development in the areas of Gastroenterology, Urology, 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 increase efficiency in your day-to-day activities

Benefits

• 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

What This Job Offers

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