Senior Clinical Studies Research Assistant

Posted 5 days ago

davitaEl Paso (TX)

Clinical Research Coordinators Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)

SENIORITY

Senior

Apply

About the role

Senior Clinical Studies Research Assistant At DaVita Clinical Research, we find that our best leaders are those who create an inspiring vision, have a desire to shape the future of medicine, and empower their team to achieve success. They enjoy tackling difficult problems and believe that the best way to solve them is through a collaborative environment that involves team efforts. They take ownership of results and instill accountability in those they lead. They are driven, compassionate, strong communicators, relationship builders, and find real fulfillment in challenging and impactful work. We are looking for a highly motivated, positive and innovative Senior Clinical Studies Research Assistant to aid in the coordination, management and conduct of nephrology clinical research trials in dialysis centers and physicians practices. DaVita Clinical Research (DCR) is a Renal Research site network conducting clinical trials across the country. DCR prides itself on a culture of growth, transparency and feedback and would want our leaders to do that same. We want a teammate who is compassionate, purposeful and motivated by meaningful work. This position is based in our El Paso, TX office, and will help support Clinical Research Coordinators and studies throughout El Paso and surrounding areas.

Essential Duties & Responsibilities:

75% - Executes clinical trial procedures and subject care while complying with Good Clinical Practice, regulatory and protocol requirements.
Communicates subject or trial procedure information to the Operations Supervisor, Charge Nurse, Investigators, Project Managers and Project Coordinators on an ongoing basis to ensure the safety and integrity of subjects and to ensure data collected for trials
Ensures compliance with Good Clinical Practice (GCP), regulatory, and protocol requirements
Records study data and maintains source documentation according to Good Documentation Practices.
Maintains knowledge of research protocols and attends education sessions provided to research staff involved in conducting trial procedures.
Supports members of study/project teams; reviews source documents, reviews clinical procedures, drafts new procedures or revisions to existing procedures
Knows, understands, and follows teammate guidelines, employment policies, and department or company procedures.
Provides consistent, regular, punctual attendance as scheduled 10% - Maintains the cleanliness and organization of the clinical research unit.
Assists with inventory, order and stocking of food, linens and supplies.
Assists with the equipment maintenance and calibration program as needed.10% - Provides input for TM performance evaluations and assists with TM orientation and training.5% - Other duties as assigned.

Minimum Qualifications: Minimum high school diploma or equivalent required Associate's degree or higher strongly preferred2 or more years of clinical research experience is required for a Senior Research Assistant level. In lieu of 2 years of clinical research experience, candidates must have some research experience combined with 3 or more years of strong phlebotomy, medical assisting, Patient Care Technician, or related clinical/medical skills. Able to work early morning, evening/night/weekend shifts as necessary to support study schedules. Attention to detail and organization skills is required Strong Data Entry skills is required Basic computer skills and proficiency in Microsoft Word and Outlook

Before you apply

Applying takes about a minute. These four things decide how fast it moves after that.

Your profile is current

It's what we read first. Occupations, seniority and locations matter more than a long history.

Two examples you can talk through

Not a portfolio — just two pieces of work where you can explain the decisions and what you'd change.

A number in mind

What you're on now and what would make you move. We negotiate better when we know both.

Your notice period

Employers plan around it, and it's the question that stalls offers most often.

Once you apply, someone reads it and calls you before anything reaches the employer — usually within two working days.