MGH is the original and largest teaching hospital of Harvard Medical School and is consistently rated one of the top hospitals in the country. I work as a CRC II on studies associated with opioid addiction, spending time with subjects as well as providing administrative support to the PI and colleagues. • Screen, obtain Informed Consent, and enroll study participants; update enrollment reports• Complete study interviews and surveys with subjects both in person and by telephone; conduct brief mindfulness sessions as per study protocol in an inpatient hospital setting• Maintain research-related files, regulatory materials, and study databases (focusing on confidentiality and privacy consistent with HIPAA guidelines)• Organize and participate in study-related meetings; prepare meeting agendas and minutes• Submit applications, amendments, reports, and other documents to internal IRB• Manage budgets, send reports to funding agencies, and handle patient study materials (such as phones and payments)

Yuma Clinical Trials, LLC is a start-up clinic based out of Arizona. I was specifically headhunted for this role based on my performance in the CRA Academy and my work with the CRC Academy. As of now, I am working on 4 studies concurrently.• Upload to, manage, organize, and oversee eRegulatory Binders using the CRIO platform; compose both study and site-based documents (ex. – FDA Form 1572, DoA logs, etc.)• Contribute to eSource by uploading files, signing off for monitors, and configuring procedures via the online platform for use by onsite CRCs during subject visits• Monitor the work of on-site CRCs to ensure it is to sponsor standards; keep in contact with sponsor and CRO monitors through e-mail• Input subject and visit data into associated EDCs; complete IRB submissions for central IRBs

DSCS CRO engages in Phase I-IV industry sponsored and investigator initiated trials. After my CRA Academy course, I did in an internship in which I participated in the management of oncological trials. • Conducted Remote Site Monitoring for Phase I and II Breast Cancer (HER2) studies• Checked the accuracy and completeness of Case Report Form (CRF) entries, source documents and other trial related records (Source Data Verification - SDV & Source Data Review - SDR)• Verified that written Informed Consent was obtained before participation in trial and that Adverse Events, Concomitant Medications, and intercurrent illnesses were reported in accordance with study protocols• Wrote Monitoring Reports to summarize monitoring activities including significant findings, deviations, deficiencies, and any recommended actions to be taken

Pactera EDGE is a global digital and technology services company that focuses on data and intelligence. My main role was to review image data to ensure the quality was high enough to integrate into an Artificial Intelligence framework according to client’s requirements.• Provided technical support to Project Management; reported deviations and resolved outstanding project issues • Trained staff on new tech; was in charge of recording/uploading training sessions for new staff• Prepared daily reports and meeting agendas; communicated daily updates for compliance adherence to project participants • Increased participant data entry compliance by 70% after implementing visual aids and graphic design, and enhanced team’s review response by 30% after applying preview option on platform coding

Vida BCN Labs is a start-up Foods & Beverages eCommerce company that specializes in CBD-based products. In my position I directly managed 10 employees (both in person and remotely), supported 4 international subsidiaries, and acted as the spokesman of the company.• Oversaw budget, and drafted monthly financial and sales reports for investors• Created the online store, managed and customized the company website, used online marketing techniques (such as SEO) to better position the company online, and tracked sales and trends• Started and ran Customer Relationship Management (CRM) systems and marketing tools, created content for e-mail marketing campaigns, and kept track of KPIs• Oversaw production chain, monitored quality control processes, and composed material safety data sheets and regulatory authority applications in the EU Region (EMEA)• Established partnerships with research institutions at the pre-clinical level; selected medical team to support patients; built collaborations in Spain, Germany, Peru, Mexico, South Africa, the UK, and France• Positioned the company to Top 5 within Spain in Google Search Engine; reduced my team’s task time by 2/3 through implementation of automation software

The University of Navarra Clinic is a leading academic and research hospital that has been listed among the top 50 hospitals world-wide according to Newsweek. For the final six months of my Master’s I worked as a CTA on studies associated with heart disease and chronic obstructive pulmonary disease.• Independently collected, reviewed, and tracked documentation for regulatory submissions; maintained electronic Trial Master File (eTMF) to ensure accuracy and detailed representation of information; performed investigator file review • Updated EDC; performed data entry; designed Standard Operating Procedures (SOPs)• Acted as communication link between investigators, team leaders, and base of operations to resolve documentation issues and deviations; handled meeting schedule• Archived documents and manuals for precise access to study information; ensured and maintained traceability of source documents

The laboratory I worked at associated with my alma mater specialized in Immunology. During my time there, I followed immunohistochemistry protocols for the study of mice brains infected with Taenia solium and utilized PCR techniques to identify molecular markers.

The CCBR is a research site that focused on industry-led trials during my time there. As a CTC Intern, I completed clinical monitoring training under the tutelage of Juan Luis Yrivarran Giorza (a well-known Research Director in Latin America).• Prepared clinical chart templates and scheduled study visits according to protocol• Packaged biological samples following IATA norms and provided support to supply and storage departments

Diagnóstica Peruana specializes in the importation and commercialization of goods (such as laboratory equipment) and services for the Health and Research sector (blood banks, pharmacies, and critical care and sterilization centers). As a Sales Representative, I created sales channels and trained new users to manage biomedical equipment.

During my Bachelor’s Degree, I worked in the UPCH Molecular Biotechnology Laboratory on a project that focused on alpaca wool improvement, and in the Human Reproduction Laboratory on a study using mice as animal models to improve fertility rate, seminal quality, and endocrine system functions.

The National Agrarian University is one of Peru’s best universities in the fields of agriculture, biological, and forestry sciences. As a Research Assistant, I studied the effect of Lepidium meyenii (maca) on sperm motility and morphology in Holstein and Brown Swiss cattle breeds and completed training in artificial insemination techniques.