Clinical Research Coordinator

Sonic Healthcare USA • Birmingham, AL

5d • Onsite

About The Position

We're not just a workplace - we're a Great Place to Work certified employer! Proudly certified as a Great Place to Work, we are dedicated to creating a supportive and inclusive environment. At Sonic Healthcare USA, we emphasize teamwork and innovation. Check out our job openings and advance your career with a company that values its team members! Quality is in our DNA -- is it in yours? You put the pro in medical laboratory professional. You’ve got problem-solving instincts, a passion for patient care, and the technical training to deliver quality results. You’re also looking for great benefits, the support of an all-star team, and an opportunity to grow your career. Join our front line of #HealthcareHeroes! Our mission is to advance the health and wellbeing of our communities as a leader in clinical laboratory solutions. The Clinical Research Coordinator will be responsible for assisting the Director of Research Operations in operationalizing clinical protocols relevant to Bio-specimen procurement initiatives. Location: Birhmingham, Alabama Days: Monday - Friday Hours: 8:00 AM - 5:00 PM Full-time: Benefit Eligible

Requirements

• A valid state driver’s license with an acceptable Motor Vehicle Report (MVR)
• Must have personal and reliable transportation
• Proof of current vehicle registration and personal automobile insurance
• Excellent verbal and written communications skills
• Experience with patient interaction
• Knowledge of basic medical terminology
• Ability to understand and abide by Food & Drug Administration: Good Clinical Practice Guidelines
• General office equipment including but not limited to personal computers, fax machines, copiers, and printers
• Proficiency in Microsoft Office applications, including Microsoft Word and Excel
• Must have personal and reliable transportation

Nice To Haves

• Nursing or Med-tech degree and certification desired.
• BA/BS science related degree preferred
• Experience working with clinical research protocols
• Experience obtaining informed consents is preferred
• Knowledge of hospital departmental policies and operations is preferred

Responsibilities

• Responsible for, recruiting, consenting, detailing and tracking eligible study subjects for clinical trials
• Introduces the details, and parameters of the study to study candidates and appropriate medical staff
• Field candidates’ questions and concerns about the study
• Obtains signed informed consent from all study participants
• Functions as the liaison between study candidates and the principal investigator
• Tracks the number of study candidates that were recruited vs. the number of successful specimen collections
• Coordinates pre-operative blood collection handling and storage when required

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Number of Employees: 5,001-10,000 employees