Cardiology Manager jobs in South Carolina
Cardiology Manager manages the cardiology department services and staff. Ensures efficient and effective departmental operations, including quality control, patient safety and regulatory compliance. Being a Cardiology Manager implements strategies and programs to deliver new technologies and services and to enhance the level of care available to patients. Requires a bachelor's degree. Additionally, Cardiology Manager typically reports to a director. The Cardiology Manager manages subordinate staff in the day-to-day performance of their jobs. True first level manager. Ensures that project/department milestones/goals are met and adhering to approved budgets. Has full authority for personnel actions. To be a Cardiology Manager typically requires 5 years experience in the related area as an individual contributor. 1 - 3 years supervisory experience may be required. Extensive knowledge of the function and department processes. (Copyright 2024 Salary.com)
Recently Added Cardiology Manager jobs
Senior Project Manager, Clinical Evaluation
- 3205 St. Jude Medical, Cardiology Division, I
-
SC, SC
FULL_TIME
- Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries. JOB DESCRIPTION: Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to: Career development with an international company where you can grow the career you dream of. Free medical coverage for employees* via the Health Investment Plan (HIP) PPO An excellent retirement savings plan with high employer contribution Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree. A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune. A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists. For years, Abbott’s medical device businesses have offered technologies that are faster, more effective, and less invasive. Whether it’s glucose monitoring system, innovative therapies for treating heart disease, or products that help people with chronic pain or movement disorders, our medical device technologies are designed to help people live their lives better and healthier. Every day, our technologies help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than 500,000 people with diabetes from routine fingersticks. The Opportunity Our location in Santa Clara, CA currently has an opportunity for a Senior Project Manager, Clinical Evaluation. This new team member will combine understanding of scientific and research methodology, medical device regulations and guidelines, and product and therapeutic area knowledge to support Regulatory Affairs medical device submissions in the EU for CE Marking of new devices and maintaining of CE Mark for existing devices in accordance with MEDDEV 2.7/1 Rev 4, MDD, AIMDD, MDCG Guidance documents, and EU MDR 2017/745. This role will support the Structural Heart product line. What You’ll Work On Manage, provide guidance, and oversight of CER Medical Writers’ development of Clinical Evaluation Reports and associated documents; set deliverable and project timelines and ensure timelines are met. Facilitate communication and exchange of documents between stakeholders (e.g., internal personnel such as Regulatory Affairs, R&D Engineering, Clinical Engineering, A&P and Marketing, Library Services, Quality Engineering, Post-market Surveillance Group, Clinical Affairs, Risk Management, Program Management, as well as external vendors such as CROs, Medical Writers and Physician Reviewers). Review, edit, and write portions, as needed, of Clinical Evaluation Reports and associated documents. Participate in and/or lead the development of regulatory responses for Notified Body questions upon review of submissions. Provide strategic guidance on regulatory requirements, pertaining to clinical data and clinical evaluations, to new product development teams and sustaining teams. Compliance with applicable corporate and divisional policies and procedures. Participate in and support internal and external audits and responses to audit findings as appropriate, in root cause analysis, preventive or corrective actions, effectiveness monitoring, and other quality metrics. Develop and update new policies, as appropriate, for processes and procedures relating to the clinical evaluation process, and train key personnel on them. Function independently as a decision-maker on CER-related regulatory issues. Required Qualifications Bachelor’s Degree in related field OR an equivalent combination of education or work experience. Minimum 6 years related work experience with a strong understanding of specified functional area. medical devices, clinical research experience, or related industry. Solid understanding and application of business concepts, procedures and practices. Will perform this job in a quality system environment. Failure to adequately perform tasks can result in noncompliance with governmental regulations. Works on problems of diverse scope where analysis of data requires evaluation of identifiable factors. Exercises judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions. Has a sound knowledge of a variety of alternatives and their impact on their business unit. Preferred Qualifications Bachelor’s Degree in Life Sciences; Master’s Degree, RN, PharmD, PhD, or MD Scientific/research background; training and degree in science, engineering, or medical fields; understanding of research design, methodology, and statistics. Thorough understanding of the EU MDR 2017/745, MDD 93/42/EEC; AIMDD 90/385/EEC; MEDDEV 2.7/1 Rev 4, MDCG Guidances on clinical evaluations, SSCP, PMCF plans and reports, and other international harmonized standards and guidelines related to medical devices, clinical studies, and quality systems. Project management and/or management of people experience. Excellent written, verbal and presentation skills in relevant areas of clinical/technical applications. Strong command of medical and surgical terminology. Demonstrated ability to identify and adapt to shifting priorities and competing demands. Highly developed interpersonal skills, and strong attention to detail. 5-7 years of experience in clinical research, clinical affairs, regulatory affairs, or quality systems, in the medical device or pharmaceuticals industry. 3-5 years of experience writing, reviewing or leading development of CERs and related documents in accordance with MEDDEV 2.7/1 Rev 3 and 4, the medical device directives (MDD 93/42/EEC; AIMDD 90/385/EEC) and the EU MDR 2017/745. Certification is a plus (e.g., RAC and PMP). Apply Now * Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan. Free coverage applies in the next calendar year. Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity. Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews. Learn more about our benefits that add real value to your life to help you live fully: www.abbottbenefits.com Follow your career aspirations to Abbott for diverse opportunities with a company that provides the growth and strength to build your future. Abbott is an Equal Opportunity Employer, committed to employee diversity. Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal. The base pay for this position is $83,600.00 – $167,200.00 In specific locations, the pay range may vary from the range posted. JOB FAMILY: Regulatory Operations DIVISION: MD Medical Devices LOCATION: United States > Santa Clara : Building A - SC ADDITIONAL LOCATIONS: WORK SHIFT: Standard TRAVEL: Yes, 5 % of the Time MEDICAL SURVEILLANCE: No SIGNIFICANT WORK ACTIVITIES: Awkward/forceful/repetitive (arms above shoulder, bent wrists), Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day) Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans. EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf Abbott is about the power of health. For more than 125 years, Abbott has been helping people reach their potential — because better health allows people and communities to achieve more. With a diverse, global network serving customers in more than 160 countries, we create new solutions — across the spectrum of health, around the world, for all stages of life. Whether it’s next-generation diagnostics, life-changing devices, science-based nutrition, or novel reformulations, we are advancing some of the most innovative and revolutionary technologies in healthcare, helping people live their best lives through better health. The people of Abbott come to work each day with relentless energy, enthusiasm and a promise to enhance the health and well-being of millions of people. They push the boundaries to help manage and treat some of life’s greatest health challenges. We invite you to explore opportunities at Abbott, to see if your talents and career aspirations may fit with our openings. An equal opportunity employer, Abbott welcomes and encourages diversity in our workforce. Follow Us: Facebook LinkedIn YouTube Twitter
- 2 Months Ago
Site Manager
- Site Manager
-
Rock Hill, SC
FULL_TIME
- RICOH IS LOOKING FOR A SITE MANAGER IN ROCK HILL! We are seeking a highly motivated and experienced Site Manager to oversee the operations of our property. As a Site Manager, you will be responsible f...
- 1 Month Ago
Practice Manager Cardiology
- Aiken Professional Association
-
Aiken, SC
FULL_TIME
- Responsibilities: ABOUT AIKEN PHYSICIANS ALLIANCE Aiken Physicians Alliance is affiliated with Aiken Regional Medical Centers, a 273-bed acute care facility offering a comprehensive range of specialti...
- 24 Days Ago
Practice Manager Cardiology
- Universal Health Services, Inc.
-
Aiken, SC
FULL_TIME
- Responsibilities ABOUT AIKEN PHYSICIANS ALLIANCEAiken Physicians Alliance is affiliated with Aiken Regional Medical Centers, a 273-bed acute care facility offering a comprehensive range of specialties...
- 24 Days Ago
Practice Manager Cardiology
- UHS
-
AIKEN, SC
FULL_TIME
- Responsibilities ABOUT AIKEN PHYSICIANS ALLIANCEAiken Physicians Alliance is affiliated with Aiken Regional Medical Centers, a 273-bed acute care facility offering a comprehensive range of specialties...
- 25 Days Ago
Clinical Manager, RN - Upstate Cardiology
- Bon Secours
-
Greenville, SC
OTHER
- With a legacy that spans over 150 years, Bon Secours is a network that is dedicated to providing excellent care through exceptional people. At every level, everyone on our teams have embraced the call...
- 22 Days Ago
Cardiology Manager jobs at Popular Companies
EKG Technician Dearborn
- St. Elizabeth Healthcare
-
Lawrenceburg, IN
- Job Description The EKG TEch performs regular EKG's, applies Ambulatory Monitors and completes any office duties that ar...
- 4/19/2024 12:00:00 AM
Supervisor of Imaging
- Renown Health
-
Reno, NV
- Position Purpose Under the general direction of the manager, the incumbent is responsible for overseeing the daily opera...
- 4/19/2024 12:00:00 AM
Cardiac Cath Lab Lead
- HCA
-
Overland Park, KS
- Introduction Are you looking for a work environment where diversity and inclusion thrive? Submit your application for ou...
- 4/19/2024 12:00:00 AM
Registered Nurse Clinician Cath and EP Lab
- Hiring Now!
-
Lenexa, KS
- Description Introduction Do you have the career opportunities as a(an) Registered Nurse Clinician Cath and EP Lab you wa...
- 4/19/2024 12:00:00 AM
Cardiology Services Manager
- BayCare Health System
-
Winter Haven, FL
- At BayCare, we are proud to be one of the largest employers in the Tampa Bay area. Our network consists of 16 community-...
- 4/18/2024 12:00:00 AM
Manager of Cardiology Service Line
- Nashville General Hospital
-
Nashville, TN
- Title: Manager of Cardiology Service Line Department Name & Number: Reports to: Director of Ambulatory Manager of Cardio...
- 4/18/2024 12:00:00 AM
Biomedical Equipment Support Specialist (Information Systems)
- U.S. Food and Drug Administration
-
Biloxi, MS
- ** Biomedical Equipment Support Specialist (Information Systems)** **Department of Veterans Affairs** ** Gulf Coast Vete...
- 4/16/2024 12:00:00 AM
Registered Nurse (RN) - Hiring Now!
- Hiring Now!
-
Lenexa, KS
- Description Introduction Do you have the career opportunities as a(an) Registered Nurse Clinician Cath and EP Lab you wa...
- 4/15/2024 12:00:00 AM
About South Carolina
South Carolina (/ˌkærəˈlaɪnə/ (listen)) is a state in the Southeastern United States and the easternmost of the Deep South. It is bordered to the north by North Carolina, to the southeast by the Atlantic Ocean, and to the southwest by Georgia across the Savannah River.
South Carolina became the eighth state to ratify the U.S. Constitution on May 23, 1788. South Carolina became the first state to vote in favor of secession from the Union on December 20, 1860. After the American Civil War, it was readmitted into the United States on June 25, 1868.
South Carolina is the 40th most extensive and 23...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Cardiology Manager jobs
$109,277 to $166,420
Most Popular Cities in South Carolina for Cardiology Manager Jobs
What does a Cardiology Manager do?
Cardiology Manager in Sioux City, IA
EviCore’s evidence-based Cardiology guidelines are based upon major national and international association and society guidelines and criteria.
January 02, 2020
Cardiology Manager in Buffalo, NY
The WVU Heart and Vascular Institute also offers technology-enabled smart clinics for cardiology patients, which bridges the traditional practice of medicine with the latest technology to provide patients with more personalized care.
January 10, 2020
Cardiology Manager in Baltimore, MD
Program Director, Interventional Cardiology Fellowship.
December 18, 2019