Would you like to coordinate research studies within a Nephrology/Dialysis population through a medical clinic and dialysis center? Bring your research expertise to us and you can be proud that you are serving in an industry that helps countless people every day! This role offers an amazing team with a collaborative work environment. If you are passionate and enthusiastic about helping people, a hard worker, and experienced in RESEARCH – please apply! We hire people that have a *positive team oriented approach* and genuinely love what they do. Our culture is very important to us. We want staff to enjoy their jobs, feel critical to the mission of our company, and thrive as a team.

This is a full-time position. Days and hours of work are Monday through Friday, 8:00 a.m. to 5:00 p.m.

Required Qualifications:
Bachelor’s degree
2 years as Clinic Research Coordinator/Assistant
1 year of pharmaceutical research trials experience
6 months of EKG and phlebotomy experience

Preferred Skills/Experience:
Overall understanding of research protocol objectives and design.
Knowledge and understanding of FDA and federal regulations regarding research.
Knowledge of GCP, ICH and HIPAA guidelines.
Ability to read, analyze and interpret general business periodicals, professional journals, technical procedures, or governmental regulations.
Ability to write reports, business correspondence and procedure manuals.
Ability to effectively present information and respond to questions from groups of managers, coworkers, clients, customers and the general public.

Essential Duties & Responsibilities:
Patient enrollment: Verify patient conformity to inclusion/exclusion and actively recruit for Studies .
Maintain accurate and complete source documents, complete CRFs or eCRFs for each patient.
Facilitate sponsor monitoring visits.
Collect urine and draw blood samples from each study patient in accordance with study protocol specifications and OSHA standards; Centrifuge blood samples and aliquots serum/plasma as specified in protocol.
Perform and document vital signs; Complete EKGs.
Management of Investigational Products: Keep daily temperature logs for room, refrigerator, and freezer to monitor excursions. Assign accurately oral and intravenous study drug medication for dispensing.
Maintain accurate dispensation and accountability records. Transport study drug to satellite site per SOP.
Regulatory Document Administration: Initiate all oral and written correspondence to IRB and sponsor including informed consent, protocol, interim status reports, advertisement and safety reports.
Assist the team in formulating study budgets.

We offer medical, dental, vision, life, disability, 401k, PTO, plus paid holidays!!
Salary: $50,000.00 – $70,000.00 annually​

Western Nephrology is a DRUG FREE WORKPLACE and an Equal Opportunity Employer. We provide equal employment opportunity to all qualified individuals regardless of race, color, religion, sex, age, national origin, citizenship, veteran status, disability, sexual orientation, gender identity, genetic information, or any other factor protected by applicable federal, state or local law.