Greg R. Profile

EXPLORAR

4,7

(2 comentarios)

Ahora estás siguiendo a

Error al seguir a usuario.

Este usuario no permite que los usuarios lo sigan.

Ya estás siguiendo a este usuario.

Tu plan de membresía solo permite 0 seguimientos. Mejora tu membresía aquí.

Dejaste de seguir correctamente a

Error al dejar de seguir al usuario.

Has recomendado exitosamente a

Error al recomendar al usuario.

Algo salió mal. Por favor, actualiza la página e intenta de nuevo.

Email verificado correctamente.

stafford,

united states

Aquí son las 4:40 p. m.

Se unió el julio 5, 2012

0 Recomendaciones

Greg R.

@grobinson10

4,7

(2 comentarios)

2,1

100%

stafford,

united states

100 %

Trabajos finalizados

100 %

Dentro del presupuesto

52 %

A tiempo

N/A

Tasa de recontratación

Writing, editing and data entry specialist

My expertise is in scientific writing for the pharmaceutical industry. Most of the writing I have done has been submitted to the FDA for review, so grammar, accuracy and time efficiency are paramount. I also have data entry experience. If you need accuracy and a quick turnaround, look no further! I can effortlessly type 40-45 wpm.

Ver todo Article Writers en United States

Contacta Greg R. sobre tu trabajo

Inicia sesión para comentar cualquier detalle por chat.

Comentarios

Cambios guardados

Mostrando 1 - 2 de 2 reseñas

Filtrar reseñas por:

4,4

$79,20 AUD

Typing from recorded voice file

yes I would hire again

Copy Typing

English (UK) Translator

Kathy A.

@KathyAshe

•

hace 10 años

5,0

$57,00 USD

write 14 short texts for children. - open to bidding

Very good job!

eBooks

Article Writing

Closed User

@sibfitnes

•

hace 10 años

Experiencia

PreMedia Global

jul 2013 - Presente

Proofread, edit and format ASCE journal manuscripts prior to publication.

DUCK FLATS Pharma

feb 2010 - feb 2012 (2 años)

Provide medical-based text assimilated from nonclinical and clinical study reports into summaries within NDA Section Modules 2.4, 2.6, 2.5 and 2.7 slated for FDA submission. Process information gleaned from drug historical data and study reports and incorporate this information into medical-based text in support of Briefing Document, NDA Sections 2.6, 2.4, and 2.7, and White Paper submission. Review articles related to proposed drug submission that support drug pharmacology, safety, efficacy, pharmacokine

Ortho Clinical Diagnostics

feb 2005 - ene 2010 (4 años, 11 meses)

Assure compliance with FDA guidelines and regulations. Prepare reports/papers on experimental testing and data analysis in cross-functional teams to achieve company strategies. Provide support for existing assays and products, new technology, and assay development. Contribute to NPC, Clinical, Regulatory, Manufacturing, and Market Dev / EBM strategies. Perform maintenance and validation activities (IQ, OQ, PQ) on analyzers. Conduct in-house safety inspections. Perform HBsAg and anti-HBs assay troublesho