Clinical Research Coordinator
Apply remote type: On-Site
locations: 06616 - DCR North Houston
time type: Full time
posted on: Posted 4 Days Ago
job requisition id: R0376819
17191 St Lukes Way Ste 100, The Woodlands, Texas, 77384-8043, United States of America
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.
Do you love patient care? Are you a LPN or RN, but are tired of the demands of working in a healthcare setting? Have you ever explored using your clinical skills differently? Clinical Research allows for a more flexible schedule for healthcare providers interested in a dynamic and fast-paced environment that is on the cutting edge of medicine.
Sound like you? Then you might be a great fit for a Clinical Research Coordinator role with DaVita Clinical Research (DCR)
We are looking for a highly motivated, positive and innovative Clinical Research Study Coordinator (Research Coordinator) to lead 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 will be based in our Shenandoah, TX (North Houston) office and coordinate and execute all aspects of late phase clinical trials in Shenandoah (North Houston) surrounding areas. Based on business needs, a flexible weekly work schedule may be available.
ESSENTIAL DUTIES & RESPONSIBILITIES:
- Accountable for the successful execution of clinical trials through all phases of the study: enrollment, maintenance and close out.
- Responsible for performing research procedures according to the study protocol and working in partnership with the physician investigator to coordinate research activities.
- Serves as a liaison between the physicians (Principal Investigator or Sub-Investigator), study sponsors and DaVita facility teammates.
- Responsible to deliver or exceed project enrollment targets for clinical research studies at their site.
- Responsible for accurate and timely data entry into the electronic data entry systems.
- Responsible for timely resolution of all data queries to meet project timelines for database lock.
- Demonstrates compliance with good clinical practice (GCP) and applicable law, and verifies that study teams comply with GCP and applicable law.
- Demonstrates adherence to DCR standard operating procedures and policies and with the standards customary in the clinical research industry.
- Understands and promotes compliance with all applicable healthcare and research regulations.
MINIMUM QUALIFICATIONS
- High School Diploma or equivalent is required.
- Bachelor's Degree is preferred.
- Minimum 1 year of clinical research experience managing studies from start up to close out or equivalent experience.
- Reliable transportation to travel between local research sites.
- 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 interactions.
- Ability 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.
- Certified Clinical Research Coordinator (SOCRA or ACRP) – preferred.
What We’ll Provide:
- Flexible weekly work schedule: This will vary and is based on current business needs.
- December Industry wellness break: (Week between Christmas and New Year’s Day)
- Comprehensive benefits: Medical, dental, vision, 401(k) match, paid time off, PTO cash out.
- Support for you and your family: Family resources, EAP counseling sessions, access to Headspace, backup child and elder care, maternity/paternity leave and more.
- Professional development programs: DaVita offers a variety of programs to help strong performers grow within their career and also offers on-demand virtual leadership and development courses through DaVita’s online training platform StarLearning.
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 careers.davita.com to learn more or apply.
At DaVita, we strive to be a community first and a company second. We want all teammates to experience DaVita as "a place where I belong." Our goal is to embed Diversity & Belonging into everything we do in our Village, so that it becomes part of who we are. We are proud to be an equal opportunity workplace and an affirmative action employer. As such, individuals are recruited, hired, assigned and promoted without regard to race, national origin, religion, age, color, sex, sexual orientation, gender identity, disability, protected veteran status, or any other protected characteristic.
Applications are accepted on an ongoing basis.
Salary/Wage Range
Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies and experience and may fall outside of the range shown. DaVita offers a competitive total rewards package, which includes a 401k match, healthcare coverage and a broad range of other benefits. Learn more at careers.davita.com/benefits.
We maintain a drug-free workplace and perform pre-employment substance abuse testing and background verification checks.
We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws.
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