“The quality of Marithea’s work has been consistently high, and her delivery of documents is always on time, many times earlier than her deadline.  Despite the fact that most of our communication is carried out via email and brief teleconferences, she always comprehends what is needed…  asking insightful questions that show she has full understanding of the process and exemplary attention to detail.  When I have a difficult assignment that needs to be completed within a tight timeframe, she is one of the first persons I consider.”
Lisa B., Vice President, Regulatory Operations
Sirion Therapeutics, Inc.

Dr. Goberville’s work is of the highest quality. We have engaged her for various types of projects including onsite conference coverage and manuscript development. She has a great deal of experience and is very clinically knowledgeable.  There has never been an occasion where we were disappointed with her work.  Simply put – “she gets it”.
Nathan K., Senior Director of Global Clinical Operations
PRIME Oncology, Inc.

“Thank you so very much for all of the work you have done on this project. You have been a rock throughout this process and a complete pleasure to work with. I heard nothing but positive feedback from the team whenever you were involved. This is can be a tough group, but they all very much appreciated everything you did. I’ve said it a hundred times, but, one hundred times more, thank you.”
Angela C., Senior Medical Writer
MedImmune, Inc.

“Thea is a take-charge person who is able to present various documents to clients as well as have direct conversations with faculty on data, etc.  She is an asset to our writing team and perfectionist in all of her work. In addition to writing skills, she is very professional on site at meetings and all interactions with clients and faculty.  When working with Thea I have a level of confidence knowing I have one of the best medical writers on my projects.”
Angela F., Account Manager
R&R Healthcare Communications

“It was a tremendous benefit to have your expertise on our team.  Your previous experience in clinical trial documentation development greatly expedited the development process and helped us to meet our commitments to the Principal Investigators.  Moreover, the fact that we received 100% approval on the documentation from our Regulatory Affairs department can be directly attributed to your extensive knowledge of the regulations and standards governing an international, multi-center trial.”
Paulena M., Technical Document Specialist
Digene, Inc.

“Thanks to Marithea for achieving the goal of a final draft CSR for our global phase 2 study ahead of that initially planned.   We appreciate your timeliness and attention to quality and detail you provided.”
Joseph P., Senior Vice President of Product Development
Cerimon, Inc.

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