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Senior Clinical Research Study Coordinator (El Paso)

Company: DaVita Clinical Research
Location: El Paso
Posted on: July 15, 2019

Job Description:

DaVita Clinical Research--(DCR), is a contract research organization and--a wholly owned subsidiary of--DaVita Inc. We use our extensive, applied database and real-world healthcare experience to assist pharmaceutical and medical device companies in the design, recruitment and completion of retrospective,--prospective and pragmatic clinical--trials.--Participating in research is the only way to bring new therapies and improved care to our patients.--Safety and continuity of care for patients participating in clinical research, high quality clinical data, and a positive experience for all parties involved in the clinical research process are top prioritiesThe Sr. Clinical Research Study Coordinator (Sr. Research Coordinator) serves to aid in the coordination, management and conduct of clinical research in DCR's Late Phase Renal research operations at regional study sites.This position will coordinate and execute all aspects of--late phase clinical trials in the--El Paso, TX area. ESSENTIAL DUTIES & RESPONSIBILITIES:Manage day to day operations at one or several research sites.--Ensure activities are completed by self or delegated to other research teammates (Clinical Research Administrators and/or Research Assistants).----Delivers or exceed project enrollment targets for clinical research studies at their site.Conduct study visits while strictly adhering to the sponsor's protocol to provide quality data to the client.Ensures accurate and timely data entry into the electronic data entry systems and resolution of all data queries to meet project timelines for database lock.--Or delegates to research assistant if available.Serves as a liaison between the Investigators, study sponsors and DaVita facility teammates.--i.e.Responsible for building a rapport with DaVita Dialysis unit teammates to maintain their engagement in clinical research projects.Resolve issues in the units as they pertain to research studies.Point person for local research team if Regional Research Manager is not available.Determines study assignments based on current study loads, experience level of team, and study difficulty.Moves research teammates between sites as needed based on workloads.Problem solves issues with senior management PRN.Ensures adherence to DCR standard operating procedures and policies and with Good Clinical Practice and other standards customary in the clinical research industry.Understands and promotes compliance with all applicable healthcare and research regulations.Accountable for marketing of study site to sponsors and /or CROs in order to obtain study awards for the site. i.e.Participates in pre-study site selection visits for placement of clinical studies. *Delegated to Regional Research Manager if available.Other duties as assigned.MINIMUM QUALIFICATIONS:Bachelor's degree strongly preferredMinimum 3 years of clinical research experience or equivalent experience is requiredExperience--coordinating late phase (phase 2, 3, 4) clinical trials.----Pharma clinical trial experience (trials sponsored by pharmaceutical companies) is strong preferredAbility to manage multiple projects, meet deadlines, and adjust priorities appropriately in an evolving work environment with shifting time frames; self-starter with high degree of initiative, urgency, and follow through.Commitment to and role model of DaVita's values with ability to demonstrate those positively and proactively to patients, teammates, management, physicians, and/or vendors (Village Service Partners) in everyday performance and interactionsAbility to manage multiple projects, meet deadlines, and adjust priorities appropriately in an evolving work environment with shifting time frames; self-starter with high degree of initiative, urgency, and follow through.Experience in managing confidential information and/or issues using discretion and judgment.Travel required up to 10% depending on business needs. Experience in managing confidential information and/or issues using discretion and judgment.Previous personnel management experience is preferredCertified Clinical Research Coordinator (SOCRA or ACRP) preferred.Here is what you can expect when you join our Village:--- A "community first, company second" culture based on Core Values that really matter.--- Clinical outcomes consistently ranked above the national average.--- Award-winning education and training across multiple career paths to help you reach your potential.--- Performance-based rewards based on stellar individual and team contributions.--- A comprehensive benefits package designed to enhance your health, your financial well-being and your future.--- Dedication, above all, to caring for patients suffering from chronic kidney failure across the nation.Join us as we pursue our vision "To Build the Greatest Healthcare Community the World has Ever Seen."Why wait? Explore a career with DaVita today.Go to http://careers.davita.com to learn more or apply.

Keywords: DaVita Clinical Research, El Paso , Senior Clinical Research Study Coordinator (El Paso), Healthcare , El Paso, Texas

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