Qureos Mentor

Cardiovascular Institute of San Diego, Inc.

Work Locations: We are hiring across multiple clinics.Location: El Cajon and La Mesa.About UsWe are a leading medical group providing exceptional cardiology and vascular care throughout San Diego County. Our clinics specialize in the diagnosis and treatment of heart and vein-related conditions, using state-of-the-art technology to improve patient outcomes and quality of life.Position OverviewWe are seeking skilled and compassionate Medical Assistants to join our growing team. As a Medical Assistant, you will play a vital role in supporting physicians and clinical staff while helping deliver high-quality, patient-centered cardiology and vascular care.Key Responsibilities<ul><li>Assist with patient assessments and evaluations.</li><li>Record vital signs and update electronic medical records (EHR).</li><li>Educate patients on treatment plans and post-procedure care.</li><li>Prepare exam rooms and maintain cleanliness and readiness.</li><li>Provide support during cardiology and vascular procedures as directed.</li><li>Work collaboratively with the healthcare team to ensure excellent patient care.</li><li>Protect patient confidentiality and comply with HIPAA standards.</li></ul>Qualifications<ul><li>High school diploma or equivalent.</li><li>Completion of a Medical Assistant program.</li><li>Prior experience in a medical office preferred; cardiology/vascular specialty a plus.</li><li>Strong communication and interpersonal skills.</li><li>Ability to work in a fast-paced environment with attention to detail.</li></ul>Preferred:<ul><li>Certified Clinical Medical Assistant (CCMA).</li><li>Familiarity with EHR systems.</li><li>Bilingual in English/Spanish or English/Arabic.</li><li>Experience with cardiology and/or vascular care.</li></ul>Benefits<ul><li>Health, Dental, and Vision insurance</li><li>Paid sick time and PTO</li><li>Growth and development opportunities</li></ul>Job Type: Full-timePay: $22.00 - $24.00 per hourBenefits:<ul><li>Dental insurance</li><li>Health insurance</li><li>Paid time off</li><li>Vision insurance</li></ul>Experience:<ul><li>Medical Assistant: 1 year (Required)</li><li>Veins: 1 year (Preferred)</li></ul>Language:<ul><li>Spanish (Preferred)</li></ul>License/Certification:<ul><li>Certified Medical Assistant (Preferred)</li></ul>Work Location: In person

Medical Assistant (Hiring for Multiple San Diego Locations)

Cardiovascular Institute of San Diego (CVISD) North County Area| Full-TimeMust be open to travel among our San Diego North County locations.San Marcos/Escondido/CarlsbadPosition SummaryThe Cardiovascular Institute of San Diego (CVISD) is seeking a skilled and compassionate Nurse Practitioner (NP) or Physician Assistant (PA) to join our growing cardiology team. This provider will support outpatient cardiovascular care through evaluation, diagnosis, treatment planning, and ongoing patient management in collaboration with cardiologists and clinical staff. The ideal candidate is motivated, patient-focused, and experienced (or highly interested) in cardiovascular medicine.Key Responsibilities<ul><li>Perform comprehensive cardiovascular patient assessments and physical examinations</li><li>Obtain and document medical histories, review diagnostics, and interpret test results</li><li>Diagnose and manage common cardiac conditions including (but not limited to):</li><li>Hypertension</li><li>Coronary artery disease</li><li>Heart failure</li><li>Arrhythmias (AFib, SVT, etc.)</li><li>Hyperlipidemia</li><li>Provide patient education and counseling on treatment plans, medications, and lifestyle modifications</li><li>Order and evaluate labs, imaging, and diagnostic studies (EKG, echocardiograms, stress tests, etc.)</li><li>Collaborate with physicians and team members to coordinate patient care</li><li>Maintain accurate and timely documentation in the electronic medical record (EMR)</li><li>Participate in care coordination, follow-ups, and referrals as needed</li><li>Ensure compliance with all clinical, safety, and regulatory standards</li></ul>Qualifications Required<ul><li>Current Nurse Practitioner (NP) or Physician Assistant (PA) license in the state of California (or ability to obtain)</li><li>National certification (AANP, ANCC for NP; NCCPA for PA)</li><li>Current BLS certification (ACLS preferred)</li></ul>Schedule / Work Environment<ul><li>Monday&ndash;Friday schedule</li></ul>Benefits <ul><li>Medical, dental, and vision insurance options</li><li>Paid time off (PTO) and paid holidays</li><li>401(k) retirement plan options</li></ul>Job Type: Full-timePay: $100.00 - $150.00 per hourBenefits:<ul><li>401(k)</li><li>Dental insurance</li><li>Health insurance</li><li>Paid time off</li><li>Retirement plan</li><li>Vision insurance</li></ul>Experience:<ul><li>Physician Assistant: 2 years (Preferred)</li></ul>Language:<ul><li>Spanish (Preferred)</li></ul>License/Certification:<ul><li>Certified Nurse Practitioner (Preferred)</li></ul>Work Location: In person

Nurse Practitioner/Physician Assistant

Our multispecialty cardiology clinic is a high-volume clinical research site at the forefront of innovative cardiovascular studies. We are consistently a top-enrolling, high-performing site across multiple trials&mdash;driven by a collaborative team culture that values mentorship, professional growth, and continuous learning.We are seeking motivated individuals who are eager to contribute to meaningful research that advances patient care and improves lives.Must be open to travel among our Northern San Diego locations, San Marcos, Escondido, and Carlsbad.Position SummaryThe Clinical Research Coordinator (CRC) reports to the Clinical Trials Manager and is responsible for the coordination and execution of clinical research studies within the Cardiology Research Unit (CRU) at CVISD.This role oversees all aspects of study operations, including patient recruitment, regulatory compliance, data collection, and study coordination, while serving as a liaison between investigators, sponsors, and internal teams.Key Responsibilities<ul><li>Coordinate and manage day-to-day clinical trial activities in accordance with study protocols and regulatory requirements</li><li>Recruit, screen, and enroll study participants; obtain informed consent and ensure confidentiality</li><li>Schedule and conduct study visits, including vital signs, questionnaires, and clinical assessments</li><li>Perform phlebotomy and process biological samples (centrifugation, labeling, storage, and shipment)</li><li>Maintain accurate and complete study documentation, including source documents, case report forms, and regulatory binders</li><li>Ensure compliance with IRB, HIPAA, GCP, FDA, and institutional guidelines</li><li>Assist with regulatory submissions, including IRB applications, amendments, and study reports</li><li>Collect and manage data from medical records, diagnostic tests, and study-specific sources</li><li>Collaborate with investigators, sponsors, and study teams to meet enrollment targets and study timelines</li><li>Enter and manage data in clinical databases with a high level of accuracy</li><li>Train and provide oversight to research assistants or support staff as needed</li><li>Participate in study meetings and provide updates on recruitment, data quality, and study progress</li><li>Support patient retention and engagement throughout the study lifecycle</li></ul>QualificationsRequired:<ul><li>Bachelor&rsquo;s degree in a relevant scientific field</li><li>3&ndash;5 years of clinical research or clinical experience</li><li>Bilingual (English/Spanish)</li><li>Strong knowledge of Good Clinical Practice (GCP) and ICH guidelines</li><li>Excellent organizational, communication, and time management skills</li><li>Proficiency in Microsoft Office applications</li><li>Ability to manage multiple priorities in a fast-paced environment</li><li>Ability to maintain confidentiality and handle sensitive information</li></ul>Preferred:<ul><li>ACRP or SOCRA certification (or willingness to obtain within 1 year)</li><li>Phlebotomy certification</li></ul>Job Type: Full-timePay: From $72,000.00 per yearBenefits:<ul><li>401(k)</li><li>Dental insurance</li><li>Health insurance</li><li>Paid time off</li><li>Vision insurance</li></ul>Experience:<ul><li>Research Coordinator: 2 years (Preferred)</li></ul>Language:<ul><li>Spanish (Preferred)</li></ul>Work Location: In person

Clinical Research Coordinator

Our multispecialty cardiology clinic is a high-volume clinical research site at the forefront of innovative cardiovascular studies. We are consistently a top-enrolling, high-performing site across multiple trials&mdash;driven by a collaborative team culture that values mentorship, professional growth, and continuous learning.We are seeking motivated individuals who are eager to contribute to meaningful research that advances patient care and improves lives.Position SummaryThe Clinical Research Coordinator (CRC) reports to the Clinical Trials Manager and is responsible for the coordination and execution of clinical research studies within the Cardiology Research Unit (CRU) at CVISD.This role oversees all aspects of study operations, including patient recruitment, regulatory compliance, data collection, and study coordination, while serving as a liaison between investigators, sponsors, and internal teams.Key Responsibilities<ul><li>Coordinate and manage day-to-day clinical trial activities in accordance with study protocols and regulatory requirements</li><li>Recruit, screen, and enroll study participants; obtain informed consent and ensure confidentiality</li><li>Schedule and conduct study visits, including vital signs, questionnaires, and clinical assessments</li><li>Perform phlebotomy and process biological samples (centrifugation, labeling, storage, and shipment)</li><li>Maintain accurate and complete study documentation, including source documents, case report forms, and regulatory binders</li><li>Ensure compliance with IRB, HIPAA, GCP, FDA, and institutional guidelines</li><li>Assist with regulatory submissions, including IRB applications, amendments, and study reports</li><li>Collect and manage data from medical records, diagnostic tests, and study-specific sources</li><li>Collaborate with investigators, sponsors, and study teams to meet enrollment targets and study timelines</li><li>Enter and manage data in clinical databases with a high level of accuracy</li><li>Train and provide oversight to research assistants or support staff as needed</li><li>Participate in study meetings and provide updates on recruitment, data quality, and study progress</li><li>Support patient retention and engagement throughout the study lifecycle</li></ul>QualificationsRequired:<ul><li>Bachelor&rsquo;s degree in a relevant scientific field</li><li>3&ndash;5 years of clinical research or clinical experience</li><li>Bilingual (English/Spanish)</li><li>Strong knowledge of Good Clinical Practice (GCP) and ICH guidelines</li><li>Excellent organizational, communication, and time management skills</li><li>Proficiency in Microsoft Office applications</li><li>Ability to manage multiple priorities in a fast-paced environment</li><li>Ability to maintain confidentiality and handle sensitive information</li></ul>Preferred:<ul><li>ACRP or SOCRA certification (or willingness to obtain within 1 year)</li><li>Phlebotomy certification</li></ul>Job Type: Full-timePay: From $72,000.00 per yearBenefits:<ul><li>401(k)</li><li>Dental insurance</li><li>Health insurance</li><li>Paid time off</li><li>Vision insurance</li></ul>Experience:<ul><li>Research Coordinator: 2 years (Preferred)</li></ul>Language:<ul><li>Spanish (Preferred)</li></ul>Ability to Commute:<ul><li>Chula Vista, CA 91911 (Preferred)</li></ul>Work Location: In person

Join Cardiovascular Institute of San Diego, Inc. and explore 4   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

Cardiovascular Institute of San Diego, Inc.

About Company

Medical Assistant (Hiring for Multiple San Diego Locations)

Nurse Practitioner/Physician Assistant

Clinical Research Coordinator

Clinical Research Coordinator