Dobbs Consulting retains the best and brightest project managers, site monitors, and auditors in the industry; our consultants boast an average of 18 years of clinical research experience in literally every therapeutic area, most notably in early-phase oncology. All of our clinical research consultants have received GCP training and carry professional/general liability coverage.
Dobbs Consulting also offers lead CRAs, medical monitors, project coordinators, regulatory document specialists and medical writers; we can fill in the gaps for each of our client's unique needs in order to provide complete coverage for their clinical trials/programs. Additionally, we have a former FDA reviewer and statistician on staff who can provide insight and expertise to our clients on various topics such as 21 CFR Part 11 compliance, protocol design, SOP writing, GCP compliance and statistical analysis.
Our clinical research consultants are identified solely through internal referrals to ensure we provide the highest caliber individuals who are results-oriented for each project team. All of our colleagues share the following characteristics and philosophies: