JACQUELENE M. CATAP
Castro Valley,CA
Summary
Seeking a challenging position where my extensive medical professional and practical experience will be fully utilized.
Overview
16
16
years of professional experience
1
1
Certification
Work History
Dialysis Charge Nurse
DaVita
Castro Valley, CA
11.2024 - Current
- Administered patient care, ensuring comfort and safety during procedures.
- Collaborated with interdisciplinary teams to develop and implement care plans.
- Educated patients on health management and medication adherence strategies.
- Monitored vital signs, documenting changes to inform treatment decisions.
- Administered medications via oral, IV, and intramuscular injections and monitored responses.
- Performed routine wound care and dressing changes on schedule.
- Promoted a safe and comfortable healing environment by addressing patient concerns promptly and professionally.
- Remained calm during high-stress, critical situations, demonstrating sustained focus and problem-solving in real-time.
- Educated patients on disease management, self-care techniques, and wellness strategies to improve long-term health outcomes.
- Implemented infection control measures that significantly reduced hospital-acquired infections.
- Collaborated with interdisciplinary teams for optimized patient treatment plans and outcomes.
- Mentored new nursing staff members, fostering teamwork and improving unit efficiency.
- Reduced medication errors through thorough double-checking of prescriptions and dosages.
- Maintained up-to-date knowledge on emerging trends in nursing practice to enhance effectiveness in delivering quality care.
- Provided emotional support to patients'' family members during critical incidents, strengthening overall trust in the healthcare team.
- Consistently adhered to strict safety guidelines while administering medications or performing invasive procedures.
- Monitored patient reactions after administering medications and IV therapies.
- Documented treatments delivered, medications and IVs administered, discharge instructions, and follow-up care.
- Implemented care plans for patient treatment after assessing physician medical regimens.
- Followed all personal and health data procedures to effectively comply with HIPAA laws and prevent information breaches.
- Led teams in driving successful patient outcomes by prioritizing standard of care and best practices.
Case Manager / Hospice Nurse
Legacy Health Care
Hayward, CA
07.2024 - Current
- Coordinated with interdisciplinary teams to ensure continuity of care and effective communication.
- Educated patients and families on end-of-life options, fostering understanding and comfort.
- Provided emotional support to patients and their families during the end-of-life process, promoting dignity and comfort.
- Collaborated with physicians to optimize medication regimens for symptom control in terminally ill patients.
- Improved patient care by developing and implementing comprehensive hospice nursing plans tailored to individual needs.
- Maintained accurate documentation of patient interactions, assessments, interventions, and responses to care.
- Educated patients and families about illness progression, treatment options, and available resources for additional support.
- Efficiently managed caseloads while adhering to regulatory guidelines ensuring compliance with Medicare conditions of participation.
Clinical Research Coordinator II
Kaiser Permanente- Clinical Trial Program
Oakland, CA
03.2022 - 11.2024
- Assisting with the informed consent process.
- Uploading forms to both internal and external sites.
- Coordinating patient visits and procedures per protocol.
- Data entry into study specific EDC.
- Responding to queries from sponsors and vendors in a timely manner
- Preparing forms to be distributed to patients.
- Coordinated patient recruitment and retention for clinical trials, enhancing participant engagement.
- Trained and mentored junior staff on best practices in clinical research methodologies.
- Facilitated site visits and audits, demonstrating compliance with Good Clinical Practice guidelines.
- Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
- Gathered, processed, and shipped lab specimens.
- Enhanced patient safety by meticulously monitoring and documenting adverse events during clinical trials.
- Collaborated with clinical staff and other healthcare professionals to support clinical trial data accuracy.
- Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
- Coordinated and monitored clinical trial activities to support timely and accurate completion of studies.
- Assessed patients'' eligibility criteria following strict adherence to inclusion/exclusion guidelines.
- Trained new team members on essential clinical research protocols and procedures, promoting a culture of continuous learning.
- Maintained compliance with protocols covering patient care and clinical trial operations.
- Managed patient recruitment, informed consent process and data entry to support trial objectives.
- Prepared and maintained regulatory documents for clinical trial submissions.
- Collected data and followed research protocols, operations manuals, and case report form requirements.
- Reduced data entry errors by implementing stringent quality control measures throughout the study lifecycle.
- Monitored patient safety throughout clinical trials and reported any adverse events.
- Participated in initiation visits and investigator meetings, implementing trials following study timelines and budgets.
- Prepared detailed informed consent documents to clearly communicate risks, benefits, expectations, rights and responsibilities related to participation in clinical trials.
- Managed study budget effectively, minimizing unnecessary expenses and allocating funds wisely.
- Coordinated with multiple departments to ensure compliance with regulatory standards, leading to successful trial audits.
Clinical Research Coordinator
East Bay Rheumatology
03.2017 - 02.2022
- Identify potential study participants and screen for study inclusion/ exclusion criteria.
- Conduct the informed consent process.
- Coordinate patient visits and procedures per protocol.
- Collect patient data on CRF and submit to the sponsor electronically.
- Communicate adverse events to the PI and report to the sponsor and the IRB as required.
- Conduct on-site monitoring visits including site qualification, initiation, interim and close out.
Certified Hemodialysis Technician
DaVita Santa Clara Dialysis
03.2014 - 11.2017
- Responsible for machine set up
- Initiation and termination of dialysis treatments.
- Patient monitoring via vital signs and machine readings.
- Record keeping, equipment monitoring and maintenance.
- Collected, labeled, and processed patient specimens for testing.
- Performed a variety of routine blood drawing procedures.
Research Assistant/ Unblinded Pharmacist / Lab Technician
East Bay Rheumatology
02.2016 - 03.2017
- Efficiently process, pack and ship clinical specimens to reference laboratories.
- Order, track, and maintain office and lab supplies.
- Perform EKG, phlebotomy, and vital signs.
- Administrative duties including filing of results, charting, and organizing clinical documents.
- Data Entry in various EDC systems.
- Preparing & mixing study drugs.
Certified Hemodialysis Technician
Fresenius Medical Care La Mesa, CA
La Mesa, CA
02.2010 - 08.2012
- Responsible for machine set up
- Initiation and termination of dialysis treatments.
- Patient monitoring via vital signs and machine readings.
- Record keeping, equipment monitoring and maintenance.
- Collected, labeled, and processed patient specimens for testing.
- Performed a variety of routine blood drawing procedures.
Education
Bachelor of Science in Nursing - undefined
Our Lady of Fatima University
01.2007
Skills
- Clinical Research Skills Good Clinical Practice (GCP)
- Clinical trial support (Phase I–IV)
- Informed consent process & patient coordination
- Case Report Form (CRF) completion & source documentation
- Electronic Data Capture (EDC) systems & query resolution
- Regulatory document management (TMF, ISF)
- IRB/IEC submissions and follow-ups
- Adverse Event (AE) & Serious Adverse Event (SAE) reporting
- Investigational Product (IP) accountability
- Audit preparation and SOP compliance
Certification
- Certified Hemodialysis Technician
- RN License
- BLS Certificate
Study Experience
- “A Multicentre, Randomized, Double-blind, Placebo-controlled, Phase 3 Study Evaluating the Efficacy and Safety of Anifrolumab in Adult Subjects with Active Systemic Lupus Erythematosus” D3461C0004 2016 - 2022
- “A Multicentre, Randomized, Double-blind, Placebo-controlled, Phase 3 Study Evaluating the Efficacy and Safety of Anifrolumab in Adult Subjects with Active Systemic Lupus Erythematosus” D3461C00009 2017 - 2022
- “A Phase 3, Multi-Center, Randomized, Double-Blind, Placebo-Controlled, 104-Week Study to Evaluate the Efficacy and Safety of Belimumab Administered in Combination with Rituximab to Adult Subjects with Systemic Lupus Erythematosus (SLE)” 205646 2018 - 2022
- “A Randomized, Double-Blind, Parallel-Group, Placebo- and Active-Controlled, Multicenter Phase III Study of the Efficacy and Safety of Olokizumab in Subjects with Moderately to Severely Active Rheumatoid Arthritis Inadequately Controlled by Methotrexate Therapy” CL04041023 2017 - 2022
- “A Multicenter, Open-Label, Phase III Study of the Efficacy and Safety of Olokizumab in Subjects with Moderately to Severely Active Rheumatoid Arthritis” CL04041024 2017 – 2022
- “A Randomized, Double-Blind, Parallel-Group, Placebo-Controlled, Multicenter Phase III Study of the Efficacy and Safety of Olokizumab in Subjects with Moderately to Severely Active Rheumatoid Arthritis Inadequately Controlled by Tumor Necrosis Factor Alpha (TNF-α) Inhibitor Therapy” CL04041025 2017 - 2022
- “A Phase 2, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of CC-220 in Subjects with Active Systemic Lupus Erythematosus” CC-220-SLE-002 2018 – 2022
- “A Phase IIb, Randomized, Double-blind Study in Subjects with Rheumatoid Arthritis Evaluating the Safety and Efficacy of Evobrutinib Compared with Placebo in Subjects with an Inadequate Response to Methotrexate MS200527-0060 2018 – 2022
Timeline
Dialysis Charge Nurse
DaVita
11.2024 - Current
Case Manager / Hospice Nurse
Legacy Health Care
07.2024 - Current
Clinical Research Coordinator II
Kaiser Permanente- Clinical Trial Program
03.2022 - 11.2024
Clinical Research Coordinator
East Bay Rheumatology
03.2017 - 02.2022
Research Assistant/ Unblinded Pharmacist / Lab Technician
East Bay Rheumatology
02.2016 - 03.2017
Certified Hemodialysis Technician
DaVita Santa Clara Dialysis
03.2014 - 11.2017
Certified Hemodialysis Technician
Fresenius Medical Care La Mesa, CA
02.2010 - 08.2012
Bachelor of Science in Nursing - undefined
Our Lady of Fatima University