Oxford Who’s Who has inducted Ms. Marsha Covelli into the highest Professional Distinction “Top Tier of Excellence Lifetime Achievement Recognition due to her expertise in drug safety, including post-marketing, clinical research and development.” Ms.Covelli has her BSN with extensive expertise in pharmaceutical industry. Ms. Covelli’s main focus of expertise is in drug safety, including post-marketing and clinical research and development. She has the ability to evaluate processes, streamline and implement changes to meet industry standards and regulatory compliance. Ms. Covelli is proactive in anticipating potential issues and provide solutions that improve efficiency with appropriate, thought-out rationale that accounts for regulatory and workload considerations. Process developments together with common sense and extensive pharmaceutical safety background have contributed to Ms. Covelli’s success in the industry. Ms. Covelli is one of few special honorees distinguished based on her professional accomplishments, academic achievements, leadership abilities, years of service, and the credentials she has provided. Marsha Covelli has displayed the ability to evaluate processes, streamline and implement changes to meet industry standard and regulatory compliances to become very successful in her industry.Ms. Marsha Covelli is interested in consulting Pharmaceutical opportunities including but not limited to the following: Serious Adverse Event narrative writing; evaluation and development to streamline processes; training personnel for safety positions; writing/developing training materials; assist with study start-up activities such as CRF development, protocol writing/review and Investigator training. Interested in the Chicago and West Coast areas. Ms. Marsha Covelli is also available for Keynote Speaking Events.
: Marsha Covelli is a healthcare professional with extensive experience in the pharmaceutical industry. Her main focus of expertise is centered on drug safety, including post-marketing and clinical research and development. She is currently a Pharmaceutical Safety Consultant at Randstad, a company offering temporary staffing, permanent placement and recruitment services. To her role, Ms. Covelli brings a proven reputation for being proactive in anticipating potential issues and providing solutions that improve efficiency. Her responsibilities include writing, editing and proofreading narratives and safety related documents for clinical study reports, protocols, protocol amendments, informed consents and other clinical and regulatory documents. Ms. Covelli’s exceptional ability to efficiently process developments, coupled with her comprehensive knowledge of pharmaceutical safety, has consistently enabled her to contribute to the growth of both her company and industry. She received her Bachelor of Science in Nursing from the University of Wisconsin--Milwaukee. Her passion for her career is equally matched by her determination to give back to charitable organizations such as Habitat for Humanity.