Vitalief is a Best of Breed Clinical Trial Solutions Company. We recruit top talent from across the clinical research industry to support our clients in the planning and execution of successful clinical trials with the ultimate goal of having a positive impact on people’s lives. We invest in our team members to ensure sustainable quality of services that meet the unique needs of each clinical trial and simultaneously provide professional development opportunities for our team members. Our high-quality Clinical Trial Advisory & Managed Services position our clients to embrace the clinical trial industry’s unprecedented and rapidly evolving needs.Our focus is helping organizations optimize their approach to running both traditional and minimal touch clinical trials through our consulting and resource management services. We are committed to delivering a positive culture, professional development opportunities, and a career path for our employees. This commitment also ensures quality services for our clients.

Fostering for a rapidly growing multidisciplinary research institution conducting trials in Rheumatology, Dermatology and Nephrology. Conducting market research to identify potential sponsors, collaborators, and strategic partnerships. Built a robust pipeline of leads and establish strong relationships with key decision-makers in the pharmaceutical, biotech, and medical device industries.Proactively seeked out and evaluate new business opportunities, including clinical trial contracts, research collaborations, and contract agreements. Developed and implemented comprehensive business development strategies aligned with the clinical research site's goals and objectives. Identified and targeted new therapeutic areas and indications for clinical trials.Attended conferences, trade shows, and networking events to expand professional networks and promote the clinical research site's capabilities. Stay updated on regulatory guidelines and industry standards related to clinical research and ensure compliance in all business development activities. Developed marketing material with IRB approved documents. Working experience with Veeva SiteVault, managing electronic documents, signatures, users, compliance adherence, system administration, system configuration etc.

Studying the health of subject participants receiving investigational products from leading pharmaceutical companies for COVID-19, Influenza, RSV and Pneumococcal vaccine clinical trials. Intake of subjects and documentation of health history, performing ECGs and phlebotomy, organization of charts, and source creation. Performing telemedicine calls with subject participants. Educate patients on current CDC guidelines for COVID-19 related procedures. Performing clinic visits as per the protocol, GCP and FDA. Adhering to regulatory trial standards and participating in subject recruitment efforts. Engage with the research investigators, pharmaceutical companies (sponsors) and contract research organizations (CRO’s) as well as the research subjects. Maintaining detailed records of studies as per FDA guideline and regulatory documentation.

Managed patient accounts including new sales and retention via remote and in person consultations. Utilized price books and SalesForce CRM to communicate prices with clients and complete transactions. Explained the benefits of hormone replacement therapy, peptides, aesthetic medicine, and sexual wellness procedures including at home medical devices. Significantly increased the retention of clients and delivered exceptional customer service. Remote consultations and management of patients nationally and internationally.

Medical scribe with growth into Chief Medical Scribe and Project Manager of the biggest Telemedicine project. Significantly improved the quality of life for physicians while completing their patients’ charts. Remotely worked with each client from multiple states. Experience working with 10 different providers in Gastroenterology, Otorhinolaryngology, Psychiatry, General and Bariatric Surgery, Urology, and Emergency Medicine. Articulate completion of patient charts with thorough and accurate documentation. Completed more than 4,000 hours in clinical training. As a project manager, I would assist in recruitment efforts and train new medical scribes.