Hire the Best Pharmaceutical Industry Specialists in Texas

PhD in pharmaceutical technology with more than 10 years experience in pharmaceutical and cosmetic industries, research, grants, patents and publications. 🌟 COSMETICS 🌟 We have a full R&D lab. My experience in cosmetics include: ★ Formulation of cosmetic products like creams, lotions, serums, toners, body butters, face and body washes, face masks. ★ Formulation of hair care products like shampoo and conditioner. ★ Ingredient selection and consultation. ★ Active ingredient consultation. ★ Preservative consultation. ★ Pricing and raw material sourcing. ★ Cosmetics regulations especially FDA regulations. ★ Cosmetic labeling and claims. ★ Advanced formulations like using microencapsulated ingredients and nanoparticles. ★ In-house microencapsulation of the active ingredients to provide protection and enhanced activity. I have formulated tens of cosmetic formulations for several clients in addition to our own company products. I am currently working as R&D chemist in a cosmetic company. This work is under this company. 🌟 RESEARCH AND GRANTS 🌟 I am basically a researcher with several successful grants, publications and patents. You may check my Google scholar profile with current h-index of 16. I can help clients in: ★ Literature search. ★ Literature curing. ★ Grant writing and application. ★ Grant revision. ★ Patent search. ★ Publication assistant. 🌟 PHARMACEUTICALS AND SUPPLEMENTS 🌟 I have more than 10 years' experience in pharmaceutical industry. I worked in R&D, production, quality control, regulatory and quality assurance (head of quality assurance for 7 years). I can help clients in: ★ Regulatory compliance. ★ Pharmaceutical formulations. ★ SOPs and document review. ★ Supplement formulations. ★ Supplement consultation. ★ Taste masking of drug and supplement formulations.

I am a highly motivated clinical pharmacist with a robust background encompassing retail, hospital, consulting, and medication management. My credentials include a Pharm.D and MBA from SUNY University at Buffalo, attesting to my commitment to both pharmaceutical expertise and business acumen. With 8 years of professional experience, I am detail-oriented, open to communication, and knowledgeable. I am passionate about leveraging my expertise to contribute meaningfully to projects and initiatives. I am available to discuss how my unique skill set aligns with your needs and objectives.

Healthcare Project Management Professional (PMP) Certified - Lean Six Sigma (DMAIC) Certified. Process Driven - Data Driven - Outcome Driven - Value Driven Project Management approach to Business Process Improvements. * Project Management (Waterfall, Agile, Lean, Six Sigma, hybrid). * Business Development (Business Plans, Market Analysis, Roadmaps, Playbooks). * Marketing (Market Research, Market Access, Market Penetration). Recent Projects: * Creation of SOP's for a window restoration business * Creation of SOP‘s and process mapping for a regional telemedicine practice. * Performed market and business development analysis. Provided marketing strategies and recommendations for a US based company with a global scope of services in information and sourcing of Active Pharmaceutical Ingredient (API). * SOP technical writing and process mapping. Creation of contracting template for pharmaceutical contracting and sourcing. * Market research projects: Mobile Infusion Therapies, Homecare Services, Pharmaceutical Market Access. * Business development projects: Consultant for 503B Compounding, Market Research, Business and Pipeline Development * Strategic sourcing and market research project: GLP-1 drug molecules Tirzepatide and Semaglutide. * Collaboration Projects: AI driven disease management programs. * Consultant to American BioPharma: market access, market research, and marketing for global activities. * Participation in market research projects as a SME in various categories (Life Science Strategy Group, LLC, Menlo Park, CA; Alpha Sights, New York, NY; GLG Research New York, NY). Experienced in both non-matrix and matrix organizations navigating business processes through a defined and customized project management approach tailored to the needs of the organization and the project using one or a combination of methodologies or frameworks. Experienced within various scopes of work * Project management * Market research and analytics * Market access and penetration * Sales and marketing - Business plans - Business playbooks * Business process creation / development * Pipeline development - Drug development - Product development * Program development - Clinical program development * Process evaluation - Root cause analysis - Development and improvement - Standard operating procedures - Training - Change management * Supply chain optimization - Sourcing and procurement - Contract negotiation and life-cycle management - Supplier relationship management, root cause analysis, value stream and outcome analysis.

I help sponsors and CROs turn clinical trial data into submission-ready deliverables. 15+ years in clinical biostatistics and statistical programming across Phase II–III and post-approval. I’m a clinical biostatistician and statistical programmer with over 15 years of experience supporting pharmaceutical, biotech, and CRO teams from protocol through submission. My background includes director-level leadership in clinical data services, along with hands-on delivery of SAPs, CDISC datasets, TLFs, and submission artifacts. I’ve worked across Phase II–III and peri/post-approval programs and am comfortable stepping in as both a contributor and a senior reviewer. Clients work with me when they need: -clear, regulator-minded statistical plans -clean, traceable SDTM and ADaM datasets -reliable TLFs with strong QC and documentation -practical guidance on define.xml, aCRF, reviewer’s guides, and Pinnacle 21 findings I’m known for fast ramp-up, direct communication, and anticipating issues before they turn into delays. I’ve led and mentored programming and biostatistics teams, supported bid development, and helped standardize tools and processes to improve consistency across studies. Services I commonly provide: -Statistical Analysis Plan (SAP) writing or review -SDTM and ADaM build support and validation strategy -Tables, listings, and figures (TLF) programming and QC -define.xml, aCRF, reviewer’s guide, and Pinnacle 21 remediation -ISS/ISE and complex integration support Tools & standards SAS (Studio, Enterprise Guide, Grid), CDISC SDTM & ADaM, SQL. I also use advanced Excel for QC, reconciliation, and sponsor-ready reporting, and SPSS for exploratory or descriptive analyses when appropriate. If you need someone who can deliver independently and think at the program level, I’m happy to discuss how I can support your study.

I am a Clinical Assistant Professor of Pharmacy Practice and an Emergency Medicine Clinical Pharmacist. I’m board-certified in Critical Care by the Board of Pharmacy Specialties. I completed post-graduate residencies in pharmacy practice and critical care at the University of Oklahoma Health Science Center and University Hospital San Antonio, respectively. These residencies allowed me to develop my research skills, medical writing, editing, and patient care skills. I spend my days either in the emergency department caring for patients and collaborating with other healthcare professionals or teaching pharmacy students at Texas A&M College of Pharmacy. I have many opportunities to be multi-faceted each day. I enjoy the research aspects of my positions and I am passionate about teaching. Some of my favorite educational topics are active learning strategies, student engagement, and writing clear and concise exam questions. I have worked on a number of different research and quality improvement projects, from implementation of pharmacy services in the emergency department to medical content review and everything in between. I have extensive experience in peer review of educational material, from presentations, lectures, and exam questions. At Texas A&M we have two campus sites which allows for ample distance learning opportunities and has given me extensive knowledge and experience in the area. I look forward to helping you with any needs you may have. I am proficient in, but not limited to: -Medical writing/ editing -Medical translation -Medical literature review, summary, and interpretation -Education material development -Exam question writing/ editing -Research protocol editing Please contact me with any questions you may have or if you would like references.

I'm a toxicologist and longevity medicine research scientist with over 14 years of training and experience in biotech, consulting, government and academia. I have a proven track record in scientific study design and execution, data collection and synthesis, testing/ analytical methodologies, experimental animal research and clinical trials. I have over 18 peer-reviewed publications with more than a 1100 citations in the fields of toxicology, pharmacology and nutraceuticals. I provide toxicology risk assessments (TRA) and biocompatibility evaluations as per various regulatory standards (FDA, ISO, state guidelines such as California Proposition 65) for medical devices, pharmaceuticals, foods, supplements and consumer products. I have successfully assisted clients with obtaining FDA 510(k) clearance for their medical devices. I also provide guidance on product formulations, scientific study design (pre-clinical and clinical), data analysis and interpretation. Clear goals, deadlines and superior delivery are very important to me. Contact me to setup a zoom call to discuss how I can help you succeed.