Clinical Research Coordinator Position Available In Lee, Mississippi

Clinical Research Coordinator CARE Institute 1542 Medical Park Cir, Tupelo, MS 38801

About CARE Institute:

CARE Institute (CardioRenalInstitute.com) is dedicated to providing quality clinical research that significantly impacts the health of patients and communities. Our mission is to advance scientific and medical knowledge within the industry. With a focus on growth and innovation, CARE Institute offers a dynamic environment with ample opportunities for professional development and career advancement. Join us at CARE Institute and be part of a dynamic team dedicated to making a meaningful difference in clinical research and healthcare. to embark on an exciting career journey with us! CARE is proud to be an Equal Opportunity Employer that values and treasures Diversity, Equity, and Inclusion. We are committed to creating an environment of dignity and respect for all our employees, patients, and families (EEO/AA).

Career Growth Opportunities:

This position offers management growth opportunities within 1-2 years, providing an exciting pathway for career advancement within CARE Institute. Job Description Clinical Research Coordinator The clinical research coordinator (CRC) is responsible for all aspects of the clinical trial and ensuring trouble-free running of all clinical trials. This is not limited to one trial at a time. The CRC will be monitoring the study to ensure that it complies with protocols, is ethically-conducted and follows regulatory standards. The CRC will work with the Recruitment Specialist and Regulatory Specialist in completing all forms, procedures, and compliance for each trial. Attention to detail and organizational skills are essential for success in this job. Responsibilities Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

• Supervises the daily activities of a study and monitors the activities of the subjects and researchers.
• Performs various medical procedures including (not limited to): patient vitals, phlebotomy, run labs, EKG, etc.
• Interacts professionally with trial compliance monitors, answering all queries & making necessary corrections if applicable.

. Dispense medication upon provider approval, provide drug accountability, and chart all actions. Maintains research records of study activity, including case report forms, drug dispensation records, or other regulatory forms as per FDA guidelines Making sure that all equipment and supplies needed for the study are in stock and in good working order.

• Attention to detail and organizational skills are essential for success in this job
• Run all Source system document generations for each trial
• Provide patient education on all trial details
• Directing the collection, labeling, storage, and transport of all specimens
• Ensuring that all equipment and supplies needed for the study are in-stock and in good working order
• Reviews and comprehends the protocol Requirements for Consideration Must be proficient in performing EKGs, blood collection, obtaining vitals, and documenting medical history.

Prior experience as a Clinical Research Coordinator is highly desired but not required. Current experience as a medical assistant is required Competencies Interpersonal Skills Manage multiple protocols Able to work

Independently Self-Motivated Ethical Practice Project Management and Detail-Oriented Stress Management/Composure Time Management Computer Proficiency:

Microsoft Office Patient focused Communication Proficiency, both Verbal and Written Supervisory Responsibility NA Work Environment This position works under normal office conditions and in a laboratory/clinic environment. The employee may be exposed to infectious diseases, blood, and bodily fluids. Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. The employee must have the ability to lift, pull, push, and manipulate equipment and patients, which requires strength and gross motor and fine motor coordination. The employee must be able to administer prescribed treatments. The position requires sitting and/or standing for long periods of time. The position requires the ability to operate a computer. Position Type/Expected Hours of Work This is a flexible position, 20-40 hours per week. Office hours are generally between 8:00 am – 5:00 pm. This position will be able to work remotely, upon approval from the Director of Clinical Research. Certain clinical trials may, on rare occasions, require after-hours and/or weekend hours for urgent work. Travel Travel for training opportunities is available but not required. EEO Statement CARE is an Equal Opportunity Employer. CARE does not discriminate based on race, religion, color, gender, or sexual orientation.

Job Type:

Full-time Benefits:

401(k) 401(k) matching Flexible schedule Paid time off Bonus pay Assistance with medical insurance Work Location In person

Job Type:

Full-time Pay:

$20.00 – $24.00 per hour Expected hours: 20 – 40 per week

Benefits:

401(k) 401(k) matching Flexible schedule Paid time off Professional development assistance

Medical Specialty:

Nephrology Schedule:

8 hour shift Monday to Friday Application Question(s): Do you currently and regularly perform all of the following on patients as part of your job duties: ECGs, vital signs, and phlebotomy (blood collection)? Can you type at least 40 words per minute? How would you rate your knowledge of medical terminology? Do you have experience collecting patient medical histories and reviewing/interpreting medical records? Which EMR or EHR systems have you used?

Work Location:

In person