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RELIANT RESOURCING

Rely on our team to help you meet your clinical research needs.

About Us

ABOUT US

Reliant Resourcing is a Veteran owned Clinical Research Consulting firm with over 18 combined years of research experience.

 

Reliant Resourcing offers consulting, training, recruitment and other research support services for clients across several therapeutic areas. Our team specializes in the pharmaceutical and medical device industries. 

Research Team

OUR SERVICES

Clinical Research Consulting
  • Clinical Research Associate

  • Project Management

  • Protocol and study document development

  • Regulatory document management (TMF management)

  • Study startup services (site selection through initiation)

Reliant Research Academy and 1:1 Career Coaching

Are you looking to obtain a professional position within the clinical research industry and unsure of where to start?

Allow our team to assist you with gaining knowledge of the industry through our training academy.  If selected, you will complete a 2-month in-depth training program that will prepare you for a role within a CRO, Sponsor, University or Hospital setting.  

Upon successful completion, a certificate will be provided confirming you've completed training regarding the below:

  • Clinical Research 101: What is research and what impact it has on healthcare

  • ICH GCP and other applicable regulations

  • Regulatory Documentation and management (ISF/TMF)

  • Understanding a Protocol and other common research documents 

  • Safety reporting guidelines 

  • Recruitment & Retention of study participants

  • Monitoring

  • Data Management 

  • Study lifecycles and phases of clinical trials

Career coaching and assistance with job placement will be provided. 

Clinical Research Recruiting/Staffing

Looking for highly qualified individuals to fill your research positions? Please let us assist you with placing quality, knowledgeable individuals within your organization.

Reliant Resourcing has built a strong network of CRAs, Project Managers, Data Managers, Data Coordinators, Study Coordinators and other research professionals. We are equipped to provide personnel to CROs, Sponsors and Sites.

All potential staff has been fully vetted with 3rd party employment verification and background checks.

Site Management Organization 
Services

As a clinical trial Investigator, it is important to have a team who can help you navigate the lifecycle of your trials. Reliant Resourcing can assist with connecting you to Sponsors for collaboration, staff to help conduct the trials and oversight by Reliant Resourcing to ensure successful execution of your study.

We are here to provide support and staff to help you meet your clinical research needs. 

TESTIMONIALS

Testimonials

“Ms. Jackson has been incredible with managing the highest enrolling site on our project. She goes above and beyond to ensure the site data continues to be monitored without getting backlogged while consistently ensuring the study metrics are met. She has been invaluable in sharing best practices for site management with our team and mentoring newer colleagues. It has been a delight to work with her. She takes initiatives and proactively works on our study deadlines and still finds time to assist at other sites to ensure we continue to meet our client's expectations and exceed them. I admire her dedication and willingness to continue learning on our complex oncology project. She's an asset to our team .”

D. Smith, Freelance CRA 

Contact Us
CONTACT
LOCATION
OPENING HOURS

Reliant Resourcing

5718 Westheimer Road, Suite 1000

Houston, TX 77057

By appointment only

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Mon - Fri: 8am - 5pm

​​Saturday: Closed

​Sunday: Closed

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