ABOUT US

WHERE WE STARTED

Founded in 2012 and headquartered in Carlsbad,  CA  servicing  pharmaceutical and biotech companies world-wide in all study phases and in multiple therapeutic areas. Comprised of experienced, specialized clinical trial experts with in-depth knowledge required to work through the special challenges and individual  needs  of  each  integral  part  of conducting a clinical trial including transition from pre-clinical to all aspects of clinical trials including  study  startup,  maintenance,  and completion.

WHERE WE STARTED

Founded in 2012 and headquartered in Carlsbad,  CA  servicing  pharmaceutical and biotech companies world-wide in all study phases and in multiple therapeutic areas. Comprised of experienced, specialized clinical trial experts with in-depth knowledge required to work through the special challenges and individual  needs  of  each  integral  part  of conducting a clinical trial including transition from pre-clinical to all aspects of clinical trials including  study  startup,  maintenance,  and completion.

Our team

Trinh Le

MBA, CEO and Founder

Trinh brings over 30 years of broad operational experience in all aspects of the biotechnology/pharmaceuticals and CRO industry specializing in early clinical development. Her natural leadership skills and ability to remove obstacles and move projects forward combined with her hands-on approach to all aspects of clinical trials has helped her establish a truly collaborative team who has a can-do attitude.

Dan Cooper

Chief Operating Officer

Daniel has over 30 years of experience in GxP environments serving in both the military and biotech/pharmaceutical industry. His unique experience in project management, clinical supplies chain management, quality systems and engineering (I&C, metrology/facility systems) allow for leveraging the skills and experience to deliver high-quality clinical research solutions for CCRC’s clients.

Deidre Capper

RN, VP of Operations

Deidre draws on her more than 30 years of drug development (CRO and pharma) and nursing experience in early clinical development to provide oversight, guidance, and implementation strategies to ensure all projects are conducted with an emphasis on subject safety and client satisfaction while adhering ICH and GCP guidelines. Her focus is on specialized rapid study start up and subject recruitment strategies as well as timeline and budget adherence.

WHAT WE DO

Let Us Provide Your Building
Blocks for Success

  • CCRC empowers clients through forging strong connections and streamlined operations to achieve faster enrollment, high-quality data, and remarkable advancements in healthcare
  • We are a virtual company resulting in lower overhead costs
  • We are reputation driven; not internal Corporate driven
    • Develop individual relationships with all functional team members
  • Our flat infrastructure allows our team to evolve with the program
  • We collaborate using a consortium of specialized experts and vendors
    • Strategically selected to match individual project needs
  • We use an integrated team member approach
    • Flexible, personalized selection of proposed team members facilitates intimate team communication for a successful study progression
  • Study execution is based on delivering quality project(s)
  • Overall, we are a ONE team partnership
    • Sponsor
    • Vendors
    • Investigative Sites

Let Us Provide Your Building Blocks for
Success

  • CCRC empowers clients through forging strong connections and streamlined operations to achieve faster enrollment, high-quality data, and remarkable advancements in healthcare
  • We are a virtual company resulting in lower overhead costs
  • We are reputation driven; not internal Corporate driven
    • Develop individual relationships with all functional team members
  • Our flat infrastructure allows our team to evolve with the program
  • We collaborate using a consortium of specialized experts and vendors
    • Strategically selected to match individual project needs
  • We use an integrated team member approach
    • Flexible, personalized selection of proposed team members facilitates intimate team communication for a successful study progression
  • Study execution is based on delivering quality project(s)
  • Overall, we are a ONE team partnership
    • Sponsor
    • Vendors
    • Investigative Sites

WHO WE SERVE

CCRC builds lasting relationships with our clients, medical professionals and third-party vendors resulting in a vast network of connections which we leverage to meet the needs of your clinical trials.

CCRC has collaborated with CROs of all sizes, domestic and international.

COLLABORATIONS:

work with us

We work towards building lasting relationships with our clients, medical professionals and third party vendors. By coming together in unison we can achieve more. Contact us to learn how we can collaborate together.

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