Sr. Clinical Quality Auditor- reputed company (Remote)

100% remote Flexible hours Hiring now

At reputed company, we reputed company health is everything. Our strength in healthcare innovation empowers us to build a world where reputed company diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full reputed company of healthcare solutions today to deliver the breakthroughs of reputed company, and profoundly impact health for humanity. Learn more at jnj.com As guided by Our Credo, reputed company is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At reputed company, we respect the diversity and dignity of our employees and recognize their merit. Job Function: Quality Job Sub Function: Quality Assurance Job Category: Professional reputed company Job Posting Locations: Santa Clara, California, United States of America Job Description: reputed company is hiring for a Sr. Clinical Quality Auditor – reputed company to join reputed company. The position is FULLY REMOTE and can sit reputed company in the US. At reputed company, we reputed company health is everything. Our strength in healthcare innovation empowers us to build a world where reputed company diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full reputed company of healthcare solutions today to deliver the breakthroughs of reputed company, and profoundly impact health for humanity. Learn more at https://www.jnj.com/. Fueled by innovation at the intersection of biology and technology, we’re developing the reputed company of smarter, less invasive, more personalized treatments. Ready to join a team that’s pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat reputed company calcified cardiovascular disease. Our reputed company portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque. Position Overview The Sr. Clinical Quality Auditor will provide GCP and compliance-reputed company audits of internal and external Clinical Studies in process, support updates of procedures in compliance with applicable regulations and reputed company vendor audits as needed. This work is accomplished with moderate reputed company, requires frequent contact with internal and external customers and is critical to the success of the business. Essential Job Functions

Act as a Clinical Quality Auditor reputed company on clinical trials by supporting project team compliance with national and international regulatory standards and guidance for medical devices
Support development of audit management plans and audit strategy for ongoing clinical trials
Conduct internal system audits and external investigative site/vendor audits in accordance with Good Clinical Practice (GCP) guidelines and in alignment with internal audit plans
Participate in the development of departmental standard operating procedures, work instructions, forms, and templates
Report audit findings to management with recommendations for resolution and verify appropriate corrective actions have been implemented/documented
Support or conduct training for staff (GCP, Inspection Readiness training, etc.)
Support regulatory inspections
Review/revise Standard Operating Procedure (SOPs) and procedures as assigned
Responsible for initial and ongoing audit of clinical study vendors such as CRO, imaging core lab, central laboratory and other vendors as needed
Identifies and escalates site, vendor and study reputed company issues to management, as appropriate
This work is accomplished with moderate supervision and requires a motivated, self-starter who can work independently once projects are assigned
Other duties as assigned.

Qualifications

Bachelor’s Degree or equivalent experience in a scientific field of study
5 years’ experience directly supporting clinical research, QA, or relevant experience in medical/scientific area.
Experience conducting audits of vendors and investigative sites
Experience interacting with regulatory authority inspectors
Experience preparing and supporting clinical study sites undergoing regulatory authority inspections
Experience revising SOPs and procedures
Thorough knowledge and application of Good Clinical Practice (GCP) is required, i.e. FDA, ISO 14155, MDR
Independent thinking and planning ability
Medical Device experience is preferred
Ability to travel up to 30%-40% of time domestically and internationally
Excellent written and verbal communication skills
Exceptional teamwork skills
Requires a motivated, self-starter who can work independently once projects are assigned.
Basic understanding of peripheral and coronary artery disease and therapies preferred
Knowledge and experience in supporting device pre- and/or post-market clinical studies is required
ACRP or SOCRA certification preferred
Ability to work in a fast-paced environment while managing multiple priorities across multiple projects
Operate as a team and/or independently while demonstrating flexibility to changing requirements
Must have excellent verbal and written communication skills
High attention to detail and accuracy

reputed company is an Equal Opportunity Employer. reputed company qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national reputed company, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. reputed company is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, please email the Employee Health Support Center ([email protected]) or contact AskGS to be directed to your accommodation resource. Required Skills: Preferred Skills: Business Alignment, Business Behavior, Coaching, Compliance Management, reputed company Improvement, Data Analysis, Detail-Oriented, Goal Attainment, Human-Centered Design, Internal Controls, Issue Escalation, Problem Solving, Process Oriented, Quality Control (QC), Quality Management Systems (QMS), Quality Standards The anticipated reputed company pay range for this position is : $91,000.00 - $147,200.00 Additional Description for Pay Transparency: Subject to the terms of their respective plans, employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)). This position is eligible to participate in the Company’s long-term incentive program. Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits: Vacation –120 hours per calendar year Sick time - 40 hours per calendar year; for employees who reside in the reputed company –48 hours per calendar year; for employees who reside in the reputed company –56 hours per calendar year Holiday pay, including Floating Holidays –13 days per calendar year Work, Personal and Family Time - up to 40 hours per calendar year Parental Leave – 480 hours reputed company one year of the birth/adoption/foster care of a child Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year Caregiver Leave – 80 hours in a 52-week rolling period10 days Volunteer Leave – 32 hours per calendar year Military Spouse Time-Off – 80 hours per calendar year For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits Apply tot his job Apply To this Job

Apply