With over two decades of experience, I am a professional in medical research, teaching, medical writing, and editing. My primary objective is to contribute my expertise to the proficient management and composition of Medical Writing documents throughout the intricate life cycle of product development.
My skill set spans a wide array of responsibilities, including the adept management, direction, and creation of regulatory and publication documents. This encompasses protocols, protocol amendments, clinical study reports, narratives, module 2 and 4 documents, briefing documents, responses to health authorities, peer-reviewed manuscripts, drug monographs, publication summaries, grants, newsletters, conference reports, training programs, brochures, and case studies.
I bring a wealth of knowledge to diverse therapeutic areas, including but not limited to CNS (epilepsy, insomnia, migraine, anxiety, depression, psychosis, bipolar disorder, MS, ADHD), oncology (gastrointestinal, hematologic, breast, prostate, melanoma, ovarian, cervical, head, neck & throat), rheumatology (rheumatoid arthritis, spondyloarthropathies), cardiovascular diseases (hypertension, dyslipidemia, obesity, metabolic syndrome), urology (erectile dysfunction, incontinence), hematology (porphyrin metabolism, hemoglobinopathies), endocrinology (hyperparathyroidism), dermatology (atopic dermatitis, vitiligo), immunology, gene therapy, and infectious diseases/anti-infectives (HIV/AIDS, blastocystosis, cryptosporidiosis, bronchiectasis).
My background encompasses both brand name and generic pharmaceuticals, as well as medical software and devices. I excel in developing content for various mediums, including hard copy, multimedia, and the internet. My commitment lies in delivering contributions that align with the highest standards in the field, reflecting a deep understanding of the intricacies within the healthcare and pharmaceutical landscape.