Meet our Clinical Staff

StudyMetrix Staff has 111 years of combined experience in clinical trials.
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Meet our Team

Timothy R. Smith, MD, RPh

Timothy R. Smith, MD, RPh

  • 34 years experience in healthcare (pharmacist, physician, researcher, medical director, corporate healthcare officer)

  • Principal Investigator or Sub-Investigator for more than 590 clinical trials and original research projects over his career

  • Experienced in all aspects of research business management and regulatory compliance

  • Extensive leadership in team building, healthcare innovation development, and grant seeking

  • Recognized and awarded for healthcare and research excellence, leadership, and lifetime achievement

Jill Stoneman, MSN, FNP-BC

Jill Stoneman, MSN, FNP-BC

  • 22 years experience in nursing including:

  • 3 years general family practice

  • 3 years medical surgical nurse

  • 15 years experience as Sub-Investigator on more than 240 clinical trials- serving under Dr. Smith

  • 15 years experience in headache management

  • Board Certified in Family Practice and a specialist in headache management

Experience Matters

Our team has completed more than 600 trials with 9,400 research patients.

Study team has worked with Electronic Data Capture (EDC) systems Inform, iMedidata, Oracle and others. Our team has also used e-Diary platforms for PHT, ERT, CRF Health, EPX and others. We are also experienced in migraine, diabetes, weight loss, cardiovascular outcomes, osteoarthritis, pain, fibromyalgia, hypertension, high cholesterol, vaccines, gastrointestinal disorders, mental health and other internal medicine trials.

Staff Credentials

  • Dr. Timothy Smith is a Certified Principal Investigator (CPI®) through ACRP

  • Mitzi Sutton is Certified in Healthcare Research Compliance (CHRC®) through the Health Care Compliance Association

  • Coordinators are all Certified Clinical Research Coordinators (CCRC®) through the Association of Clinical Research Professionals (ACRP)

  • All the staff has extensive and ongoing training Good Clinical Practice (GCP)

  • All staff is trained on HIPAA

  • We have Standard Operating Procedures (SOPs) that have been developed using the FDA and ICH guidelines

  • IATA trained for laboratory shipping

Clinic Capabilities

  • Ability to perform blinded and unblinded studies

  • Ablility to perform injection and IV infusion studies

  • Dedicated drug storage with refrigeration, freezer and backup generator

  • Dedicated monitor area

  • Secure storage for case report forms

  • Electronic storage (diaries)

  • Phase I/II – IV

  • Extended stays up to 6 or 8 hours

  • Laboratory capabilities including PKs

  • Dietary consultations

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