Serving emerging life science companies developing novel therapeutics and devices
Call us: 1.302.345.8111
  • Clinical Trial Services
    Clinical Operations Services for
    Emerging Biotech and Device Companies
  • Clinical Trial Planning
    - Realistic accrual planning - Proven approach to feasibility - Enrollment validation
  • Clinical Trial Management
    - Streamlined study initation - Careful monitoring of milestones - Active accrual assessment
  • Clinical Trial Staffing
    - Experienced CRAs- Active recruitment monitoring - Prioritizing site communication - Site relationship management

Who we are

We absolutely believe that trial efficiency is created when dedicated people successfully execute a customized study start-up and accrual plan.

About Us

Why we do it

Drugs in development for oncology indications had the lowest overall clinical trial success rate of all therapeutic areas in development since 2004..

Our Vision

What we do

Protocol assessement, comprehensive site selection, partient accrual strategy planning. We aim to achieve your accrual timelines.

Our Services

More about Adjuvant

  • Our Philosphy
  • Join Our Company
  • Trial Rescue Services

Adjuvant Research Services is a clinical operations services firm serving emerging life science and medical device companies. We strongly believe that Sponsors who invest in meticulous study planning can, in fact, achieve critical enrollment timelines. We specialize in creative study start-up, feasibility planning and patient accrual strategy planning and management. Development phase Sponsors can improve study initiation cycle times and achieve patient accrual goals while maintaining data integrity. Early study planning and consistent implementation does work. Let us show you how.

We believe that developing successful relationships with investigational sites is a critcal and key component to clinical trial success. Adjuvant is always seeking research professionals with oncology and vision care clinical trial experience. We value superb interpersonal skills in our people. Can you engage, problem solve, negotiate and gain the respect of study site personnel? If so, we want to speak with you. To join our growing company or to be considered for contract opportunities, please complete our contact information form Registration Form. We would love to learn more about you.

Investigational sites struggling to meet accrual timelines need help. Setting up sites to achieve success is a function of understanding and dealing with the specific operational limitations as well as the particular difficulties presented by your complex protocol. Adjuvant will quickly assess, create and implement protocol specific and site specific remedies to get your important program back on track.

Using insights gained from helping dozens of Sponsors and rescuing hundreds of studies, we craft multiple creative and cost effective tools and solutions to ameliorate your study performance issues.

Meticulous clinical trial planning includes:

  • Strategic investigational site selection
  • Enrollment validation activities
  • Protocol optimization focus groups and simulation workshops
  • Mapping potential clinical trial subjects pathway to enrollment
  • Indentifying potential sources of subjects using novel and creative tools
  • Developing recruitment action plans for confident consenting
  • Assessing a protocol's clinical relevance to a site's operational reality