Oncology Clinical Research

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Clinical Research Consulting Services
for Pharmaceuticals Biotech & Devices

 

Oncology Clinical Research provides consulting services in the areas of adverse event reporting, GCP auditing, field monitoring, medical writing, project management, site coordination, CRA training, regulatory compliance and regulatory submissions. Temporary in house support is also offered.

Since 1984 Scott W. Maurer, senior consultant, has gained valuable experience in both the Pharmaceutical/Biotech R&D arena as well as CRO and contract settings. His diversity of therapeutic areas, creativity, ingenuity, and attention to key detail directly contributed to more than 12 successful regulatory submissions.

Scott W. Maurer
Senior Consultant

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   THERAPEUTIC EXPERIENCE:

Aids
Anti-infective
Artificial Blood
Cardiovascular
CNS-(Alzheimers)
CNS-(Depression)
CNS-(Stroke)
Devices
Gastrointestinal

Infectious Diseases
Metabolic - (Diabetes)
Oncology
Ophthalmology
Pain
Respiratory
Reproductive Medicine
Transplantation & Rejection

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   FEE SCHEDULE:

A sliding scale is offered based on several factors. ($75 - $105 per hour*)
These factors include autonomy provided, work location, and length of contract.

(* My location, my choice of hours is less than on-site with intense supervision wanting product yesterday.)

 

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