Our team of clinical research professionals has extensive experience, many with 15 to 20 years in the industry. They understand the challenges faced by companies in navigating the clinical trial process and use practical experience to overcome these challenges. Our clinical research professionals have spent their careers in life science positions as research coordinators, CRAs/monitors, project leaders, medical writers, or Quality Assurance personnel, providing you with a wealth of knowledge and experience.
Modoc is led by Julienne Orr, founder, owner, president/CEO, and principal consultant of this privately held, woman-owned company providing clinical study support services. Ms. Orr’s vast pharma/CRO/ARO experience, as well as her work partnering with Modoc clients over the past 12 years, make her an industry-leading professional who is ready to partner with you to improve your clinical studies.
Since its founding in 2005, Modoc has worked with large pharma/biotech companies, mid-size pharma/biotech companies, large CROs, and small/mid-size CROs. No matter the size, each of our clients receives focused service, with open and frequent communication. We value our relationships with our clients and their other vendor partners, and work in a collaborative and cooperative manner to achieve your goals. Contact us for references who will speak to our success, experience, and professionalism helping clients.
Modoc’s therapeutic experience includes oncology, dermatology, CNS/neurology, gastrointestinal, women’s health, and generics.
Modoc has worked on the various phases of clinical studies, from Phase I through Phase 3. We have experience in all types of studies, including dose-escalation/expansion, safety and efficacy, PK/PD, ADME, food-effect, thorough QT, and more.
See how you can benefit from our expertise, contact us today.