BEGIN YOUR JOURNEY in clinical research.

introduction to clinical research

8-session curriculum

  • SESSION 1: Introduction to Clinical Trials (History, FDA, GCP)

  • SESSION 2: Introduction to Clinical Sites (PI, CRC roles)

  • SESSION 3: Introduction to the Clinical Research Associate role

  • SESSION 4: Introduction to Pharmacovigilance (Safety)

  • SESSION 5: Introduction to Data Management - Electronic Data Capture

  • SESSION 6: Introduction to Investigational Product / Laboratory

  • SESSION 7: Introduction to Regulatory Affairs - Institutional Review Board

  • SESSION 8: Introduction to Monitor Visit Reports, Metrics.

  • EXAMINATION

  • CV development

Get access to a multi-chapter course that ladders up to specific focuses and goals.

Unlock your pathway to success in clinical research with our intensive 8-session course!

Dive deep into the fundamentals of clinical research and gain practical experience using industry-standard platforms. Upon successful completion of our comprehensive online examination.

Pre-requisites:

  • Have completed (or completing by the end of the last session) a Bachelor’s in Science (B.S) degree from an accredited university.

Contact us for details!

learn all about clinical research in 8 sessions!

1:1 COACHING

If you’re looking for something completely integrated and tailored to your specific needs, 1:1 coaching might be the right step for you. Learn what you can expect in a session or book a free consultation today.

CLINICAL SITES

We collaborate with pharmaceutical companies (Sponsors), clinical research sites, contract research organizations (CROs), academic research organizations (AROs) and others to help these organizations conduct their research efficiently and on schedule.


Collaborating with us can provide numerous advantages to clinical research teams, such as:

  • Identifying new studies to participate in

  • Facilitating contract and budget negotiations with the Sponsor or CRO

  • Assembling and training the study team

  • Providing support throughout the study process, from site selection to study closeout

  • Enhancing subject recruitment

CLINICal research associate (CRA) allocation

We excel at strategically matching highly qualified Clinical Research Associates (CRAs) to research projects worldwide, including North America, South America, and Europe. Our meticulous allocation process prioritizes both project requirements and individual CRA expertise, guaranteeing seamless trial monitoring, robust data integrity, and strict regulatory compliance. By aligning CRAs with specific therapeutic areas, geographical needs, and specialized skill sets, we optimize project efficiency and empower our CRAs to contribute significantly to cutting-edge research.