MINETTE JOY C. EVANGELISTA, USRN

ADDRESS: Unit *E, F. Antonio Street, Salapan, San Juan City, Philippines 1500 E-MAIL: adn6pb@r.postjobfree.com

MOBILE: +639*********

Accreditation and License

January 2018 Northern Mariana Islands NCLEX-RN Board Passer License Number: R18100

Endorsed to Texas Board of Nursing

License Number: 978002

June 2007 Philippine Nursing Licensure Examinations Board Passer License Number: 0440289

Experiences and Qualifications

3 May 2021 to Present Cancer Center Nurse I

Cardinal Santos Medical Center

Duties and Responsibilities: • Patient Management

• Identify and analyze patient's personal and health profile making use of records and collections of patient's data

• Identify and assess nursing problems - physical, mental and spiritual

• Plan, implement and deliver nursing care according to priorities

• Give health instructions to patients and relatives

• Discuss and clarify to patient's relatives their role in promotion of therapy and rehabilitation

• Give appropriate instructions regarding tests and procedures

• Technical

• Accurately list supplies/medications used by patient

• Carry out physician's orders in conformity with policies and legal limitations

• Assist in performance of procedures and tests

• Use sound judgment in adopting nursing procedures and techniques

• Execute nursing procedures and techniques – medication, vital signs, treatment, specimen collection, patient hygiene, nutrition and elimination

• Perform the following medical procedures accurately – setting up of IV infusion, changing IV line, discontinuing IV infusion

• Administration of drugs through IV - IV push, incorporation of drug into IVF/Soluset, piggy back

• Collaboration

• Ensure proper functioning, maintenance and availability of equipment and facilities

• Create and maintain therapeutic environment by providing privacy and comfort and safety

• Participate in the implementation of cost-cutting measures

• Promote good interpersonal relationships among co-workers

• Taking part in formulating, revising and modifying nursing procedures and techniques

• Communicate and act as liaison between patient, physician and other hospital personnel

• Report/Record Management

• Update the patient's protocol index cards and treatment flow sheets in the patient charts

• Practice the standard of accurate recording and reporting and make certain that all patient's records are complete and well accounted for

• Ensure that inventory of supplies and linen ins update regularly

• Ensure that “no losses” are incurred by the unit

• Evaluate care given and reports pertinent observation to proper individuals

• Report to charge nurse any unit damages/losses

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• Report to charge nurse all defects/problems of machine/equipment and ensures regular maintenance of these

• Other

• Performs other functions as may be assigned by immediate superior from time to time

10 June 2019 to 25 April 2021 Senior Process Executive/Utilization Management Reviewer Cognizant Technology Solutions

Duties and Responsibilities: • Performs utilization management reviews in accordance to federal and state mandated regulations. Maintains compliance with regulatory changes affecting utilization.

• Performs UM reviews for inpatient and outpatient services and home health care according to URAC standards and client requirements and policies.

• Reviews UM requests for services against established clinical review criteria, referring cases not meeting criteria to a physician reviewer.

• Adheres to Department of Labor, stare and company UM time frame requirements.

• Coordinates physician reviewer referral as needed and follows up timely to obtain and deliver results.

• Tracks status of all utilization management reviews in progress.

• Releases UM determinations to claim stakeholders following client- established protocols.

• Serves as first level contact for customer complaint resolution and responds to in-bound calls pertaining to UM reviews in a timely manner.

• Maintains confidentiality of all information, policies and procedures as required by the Health Insurance Portability and Accountability Act

(HIPAA) protocols.

• Performs other duties as assigned or required such as:

• Provide additional support to new hired reviewers

• Cross trained to other processes to be a back-up whenever needed January 2016 to June 2019 Clinical Review Specialist PPD Pharmaceutical Development Philippines Corp.

Therapeutic Area: Oncology, Psoriasis, Cardiovascular and Vaccine Duties and Responsibilities: • Reviewed patient data in accordance with GCP, SOPs and Data Validation Manuals (DVM).

• Reviewed patient data in accordance with the Clinical Listings Review Plan in the DVM.

• Identified data issues and worked with the team and study sites to resolve and ensured data accuracy according to departmental operating procedures.

• Ensured applicable data review activities were conducted accurately, and related deliverables were completed to quality expectations, within budget and on time.

May 2015 to December 2015 Assistant Manager, Research VMV Skin Research Centre + Clinic

Therapeutic Area: Dermatologic and Cosmetic Studies Duties and Responsibilities: • Assisted Investigator(s) in formulating and writing research protocols, preparing informed consent forms, designing data collection forms and managing paperwork and applications.

• Aided in budget planning for proposed clinical trial costs and coordinated conduct of the assigned clinical trial.

• Performed clinical and study procedures as per study protocol as training and experience allows such as:

• Clinical assessment

• Vital signs taking

• Documentation of skin conditions using photographs

• Administration of medications

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• Encoded all data in a specified database that was required by the study and/or sponsor.

• Coordination of several individuals and delegating protocol related tasks to members of the group during the actual clinical trial procedures

• Ensured the conduct of clinical trials according to the applicable Good Clinical Practice (GCP) guidelines, applicable regulations, Protocol and Standard Operating Procedures (SOPs) at all times.

• Other duties as may be required & as training and experience allow such as:

• Clinical assessment

• Vital signs taking

• Assisting doctors during dermatological procedures during peak clinic hours

January 2014 to March 2015 Associate Regulatory and Start Up Specialist Quintiles Philippines, Inc.

Therapeutic Area: Phase II Diabetes Mellitus Type II Study; Phase III Rheumatoid Arthritis and Systemic Lupus Erythematosus Studies

Duties and Responsibilities: • Prepared Ethics Committee and Regulatory Authority Submissions and initiated and completed Contracts Negotiation: Contracts legal terms & budgets, executes and files contracts and management of Document collection for Investigational Product release.

• Maintained project tracking in in-house system until Site Initiation. August 2012 to January 2014 Senior Clinical Trial Assistant Quintiles Philippines, Inc.

Therapeutic Area: Phase I Tuberculosis Study; Phase III Vaccine, Lupus Nephritis and Heart Failure Studies

Duties and Responsibilities: • Assisted Clinical Project Manager (CPM) and Clinical Research Associates

(CRAs) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines and acted as a central contact for the clinical team for designated project communications, correspondence and associated documentation.

• Performed assigned administrative tasks to support team members with clinical trial execution and maintained Trial Master Files, study documentation and communication

• Worked daily with Microsoft Word, Excel and Outlook February 2012 to March 2012 Clinical Research Assistant/Coordinator St. Luke's Medical Center

Therapeutic Area: Phase I Medical Device Study for Alzheimer’s Disease Duties and Responsibilities: • Assisted Investigator(s) in formulating and writing research protocols and in preparing informed consent forms, designing data collection forms and managing paperwork and applications.

• Aided in budget planning for proposed clinical trial costs. February 2008 to August 2012 Clinical Research Nurse Research Institute for Tropical Medicine

Therapeutic Areas: Vaccines and Pediatric Nutritional Studies Duties and Responsibilities: • Coordinated conduct of the assigned clinical trial, prepared of study related documentation and reviewed and completed of study documents (Case Report Forms and Source Documents) and performed clinical and study procedures as per study protocol as training and experience allows such as:

• Vital signs taking

• Clinical assessment of the patients for eligibility to the study and during the course of the study

• Physical Assessment

• Providing information regarding the goals of the study

• Providing information regarding the patient's/caregiver's right Page 3 of 4

and responsibilities

• Explaining and obtaining consent

• Educating the patient and/or caregivers of the procedures once they are home

• Documentation of the signs and symptoms based on the patient's/caregiver's reports and from clinical assessment

• Administration of medications/vaccines.

• Aided in stool collection as required by the study.

• Encoded all data in a specified database that was required by the study and/or sponsor.

• Handled between 15 to 40 patients and/or caregivers every clinic visit

• Detailed review of subject and study documentation, case report form

(CRFs) and source documents and ensured the conduct of clinical trials according to the applicable Good Clinical Practice (GCP) guidelines, applicable regulations, Protocol and Standard Operating Procedures

(SOPs) at all times.

Education

June 2003 to March 2007 University of Santo Tomas – España, Manila Bachelor of Science in Nursing

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