Hire Regulatory Writing Experts in United States

As a scientist with over 20 years experience of project management, technical writing, teaching and the regulatory landscape; I have developed ...

Industry leader with 20+ years of expertise in the clinical trial, drug development space. PhD Biotech, Adv Dip French Literature. Have represe...

I am a US-based doctor of pharmacy with board certification in pharmacotherapy (BCPS). I bring a clinician's eye to your medical writing p...

I’ve graduated from the University of Bridgeport’s Nutrition Institute, where I received my Master of Science in Human Nutrition. Befo...

Pharmaceutical/Nutraceutical/Food Formulation Scientist with 20+ years of experience developing soft chews, tablet and capsule products, chewab...

Mary Beth Ritchey, PhD, FISPE has spent more than 15 years in government, industry, consulting, and academia in better understanding medical pr...

My expertise is development of clinical evaluation reports (CERs). This includes experience with literature searches, post-market surveillance,...

More than 17 years working as Health Care Consultant for different companies and agencies, as well as a professor from a private and public un...

I am an experienced health professional, having 6+ years of thorough working experience in clinical research and the therapeutic research indus...

I have reviewed 2000+ research protocols and helped created hundreds of consent forms for complex research studies. I'm an expert with the...

20+ years of clinical research experience, including expertise in the principles and practices of clinical trial research, including management...

I worked for a large healthcare organization conducting NIH medical research for over 10 years. I served as the lead Clinical Research Coordina...

My pre-doctoral, doctoral and post-doctoral training collectively focused on cell and molecular biology approaches to dissect mechanisms of dev...

Experience in craniofacial genetics, medical imaging on postdoctoral level. Experience in market research, intellectual property landscape and ...

Loren DeVito, PhD, is a science and medical writer with expertise across a wide range of therapeutic areas, including oncology, neurology, card...

I am a trained medical and regulatory writer, experienced and specialized in Precision Medicine Oncology. I also have expertise in Neuroscienc...

I am an ambitious and published scientist who is experienced in many scientific disciplines including Biology, Chemistry, and Engineering. I ha...

• Staff Research Associate - UCSD Shiley Eye Institute (Current): Project focusing on understanding retinal ischemic diseases, specifically the...

My basic research experience is in tissue engineering in the neural application. I have experience in both in vitro and in vivo experiment desi...

Experienced medical writer with expertise in clinical writing (clinical trial protocols, study reports, IBs, ICFs) and regulatory writing (IND,...

Executive Management |Project, Program, Portfolio Management - PMO ~ Robotics |Biotech | Pharma | Medical Devices | FDA I develop and delive...

-Biomedical scientist with over 5 years of research experience and a strong background in a wide range of research areas such as Oncology, Mole...

More than 15 years of experience in Healthcare Services Delivery, Public Health surveillance, and defining strategic plans based on in-depth ph...

Motivated, self-driven entrepreneur, consultant to regulatory affairs and QC/writing departments within the medical, biotech and pharmaceutica...

My name is Linda Minkow. I'm a food scientist with a Masters in Food Microbiology from Rutgers University. I have over 15 years of experien...