Magela Fernandez Perez

• Administered medications and treatments to patients according to physician prescriptions.
• Educated patients and families on health conditions and self-care practices to promote understanding and adherence.
• Monitored vital signs and reported changes in patient conditions to the team.
• Assisted in conducting research studies to enhance patient care practices.
• Maintained accurate medical records in compliance with regulatory standards.
• Provided emotional support and counseling to patients, enhancing recovery and coping strategies.
• Utilized critical thinking skills to assess clinical situations quickly and accurately.
• Collaborated with healthcare professionals to develop individualized treatment plans, ensuring comprehensive patient-centered care.
• Assessed, planned, implemented and evaluated nursing care for assigned patients.
• Maintained a safe environment for all patients by adhering to infection control policies and procedures.
• Documented patient progress notes accurately and efficiently in the electronic medical record system.
• Administered medications and treatments, monitoring patients for reactions and side effects.
• Advocated for patients by supporting and respecting basic rights, values, and beliefs.
• Evaluated effectiveness of interventions through ongoing assessment of patient responses.
• Evaluated patients, recognized and addressed complications and coordinated treatment with other members of critical care team.
• Adhered to infection control procedures to facilitate safe, clean patient environment.
• Recorded patient condition, vital signs, recovery progress and medication side effects.
• Provided patient care and education to patients with chronic illnesses.
• Assessed patient needs, prioritized treatment, maintained patient flows and assisted physicians with non-invasive procedures.
• Updated charts throughout shifts with current, accurate information to maintain strict recordkeeping standards.
• Participated in multidisciplinary team meetings to discuss patient care plans.
• Oversaw patient admission and discharge processes to coordinate related paperwork.
• Provided patient and family health education focusing on self-management, prevention and wellness.
• Counseled patients regarding medication side effects or lifestyle changes necessary for improved health outcomes.
• Created, implemented and evaluated patient care plans with medical team.
• Maintained personal and team compliance with medication administration standards and patient care best practices.
• Ensured compliance with standards of professional practice as well as state and federal regulations related to health care delivery services.
• Demonstrated knowledge of current trends in nursing practices by attending continuing education classes or seminars.
• Conducted intake assessments with patients and relatives to gather case history.

Conducted phase 2b randomized controlled observer-blind multi-center study on Novartis meningococcal ABCWY vaccine immunogenicity and safety in adolescents.

Executed open-label safety study assessing adrenal suppression potential and pharmacokinetics of Topicort topical spray in pediatric patients with plaque psoriasis.

Led phase III stratified randomized observer-blind controlled clinical study evaluating safety, immunogenicity, and efficacy of adjuvanted quadrivalent influenza vaccine in children aged six to seventy-two months.

Managed phase 3 randomized double-blind placebo-controlled trial of linaclotide for twelve weeks in patients with chronic idiopathic constipation.

Directed randomized double-blind vehicle-controlled dose-ranging phase II study evaluating efficacy and safety of desoximetasone shampoo in patients with moderate to severe scalp psoriasis.

Oversaw phase II double-blind placebo-controlled study on safety and efficacy of topical patch AB001 in chronic low back pain patients after two weeks of daily administration.

Facilitated randomized double-blind parallel-design study comparing therapeutic equivalence of diclofenac sodium gel 3% to Solaraze gel for actinic keratosis treatment.

Coordinated 52-week double-blind placebo-controlled study of rezlizumab in patients with uncontrolled asthma and elevated blood eosinophils.

• Coordinated clinical trial activities to ensure compliance with regulatory standards.
• Coordinated participant recruitment and enrollment strategies to enhance study engagement.
• Developed study protocols and maintained accurate documentation throughout trials.
• Facilitated communication between research teams and external stakeholders.
• Monitored participant safety and reported adverse events promptly.
• Analyzed and interpreted data to substantiate study conclusions and inform reporting.
• Communicated effectively with investigators, study staff, sponsors, vendors, IRB personnel, and other stakeholders throughout the life cycle of the trial.
• Maintained accurate up-to-date tracking logs for all aspects of clinical research activities including but not limited to adverse events, serious adverse events, concomitant medications, lab results.
• Collaborated with sponsors and investigators to carry out efficient and fully compliant research trials.
• Adhered to standards in areas involving data collection, research protocols, and regulatory reporting.
• Assisted in the preparation of Institutional Review Board submissions for clinical trials.
• Performed routine site visits to verify compliance with protocol requirements and identify potential areas for improvement.
• Reviewed medical records for accuracy of source documentation prior to database lock.
• Collaborated with internal departments such as Regulatory Affairs and Data Management to ensure that all studies were conducted in accordance with ICH-GCP guidelines.
• Organized investigator meetings; developed meeting agendas; created presentations; tracked action items from meetings; coordinated follow-up communications after meetings.
• Developed and maintained accurate and timely study databases.
• Performed patient assessments, collected and analyzed data, and prepared reports.
• Provided guidance on Good Clinical Practice regulations and other applicable regulatory standards.
• Conducted quality assurance audits at research sites to ensure adherence to protocols, SOPs, regulations, guidelines.
• Prepared informed consent forms for review by ethics committees.
• Assisted in preparing periodic reports summarizing progress of clinical studies.
• Provided training to study staff on protocol requirements and GCP regulations.
• Conducted screening interviews to determine eligibility of possible subjects.
• Took vital signs and collected medical histories as part of study protocols.
• Monitored subject enrollment and tracked dropout details.
• Ordered and managed medications for clinical studies to ensure availability for participants.

• Oversaw patient care and administrative duties in high-volume healthcare setting, ensuring efficient operations and patient satisfaction.
• Coordinated patient preparations for EKG, PFTs, and physical examinations, enhancing collaboration with healthcare providers.
• Implemented a new patient scheduling system, reducing wait times by 25%.
• Trained and fostered 8 new staff members, ensuring adherence to clinic protocols and patient care standards.
• Led a project to digitize patient records, enhancing data accuracy and accessibility.

• Coordinated and contributed with physicians to streamline patient flow, resulting in a 20% increase in daily patient capacity.
• Supervised team of clinicians to enhance patient care and clinical efficiency.
• Developed continuous education program for staff, enhancing clinical skills and patient interaction.
• Organized community health fairs, providing health screenings and education to over 500 individuals.

• Increased patient care efficiency by 15% by executing direct collaboration on a maternal care research project.
• Led patient care initiatives and supported administrative functions to enhance overall healthcare delivery.
• Facilitated patient education sessions to improve understanding of treatment plans and adherence to medication.
• Managed inventory and coordinated supply ordering to maintain clinical operations while optimizing resource use.