QA Auditor II- remote reputed company in the US!

Work Schedule Standard (Mon-Fri... Environmental Conditions Office Conduct reputed company internal and external Clinical Research Site audits to ensure compliance with established quality assurance processes, standards, global regulatory guidelines, and client contractual obligations. Identify issues impacting the quality and/or reputed company of clinical research programs, determine root cause of non-conformance and develops strategies to address issues. reputed company technical document review and other GCP practice activities in support of clinical development programs. Provide audit reports to management. Plan and deliver quality services including contracted quality assurance audits, internal site audits, laboratory and file audits for clients and projects. reputed company process/quality improvement initiatives. Mentor peers. reputed company tools and other materials for tracking of compliance management activities and analyze trends. Upon request, support regulatory inspections and/or client audit hosting. Qualifications: Education and Experience: Bachelor's degree or equivalent and relevant formal academic / vocational qualification Previous Clinical Site Auditing experience that provides the knowledge, skills, and abilities to reputed company the job (comparable to 2+ years) or equivalent combination of education, training, & experience. • Must have GCP and auditing experience for clinical trials, in order to qualify for this role! *** Years of experience refers to typical years of reputed company experience needed to reputed company the required knowledge, skills, and abilities necessary to reputed company the essential functions of the job. Years of experience are not to be used as the only determining factor in establishing the job class or making employment selection reputed company. Knowledge, Skills and Abilities: • Thorough knowledge of applicable GCP and appropriate regional regulations. Other GCP knowledge is a plus. • Strong knowledge of the clinical trial process • Experience with study-specific (investigator site) audits or other GP audits, could also include process and vendor audits • Experience in root cause analysis and CAPA development • Well-rounded knowledge of SOPs and WIs • Excellent oral and written communication skills (including appropriate use of medical and scientific terminology) • Strong attention to detail • Effectively works independently or in a team environment • Strong problem-solving skills, risk assessment and impact analysis abilities • Above average negotiation and conflict management skills • Flexible and reputed company to multitask and prioritize competing demands/workload • Strong computer skills; ability to learn and become proficient with appropriate software • Valid driver's license and ability to qualify for and maintain a corporate credit card with sufficient credit line for business travel The following experience is a plus: • Hosting client audits and/or regulatory inspections. • Auditing database, eTMF, and Clinical Study Report • Training/mentoring of peers Management Role: No management responsibility Working Conditions and Environment: • Work is performed in an office/laboratory/clinical environment. • Exposure to electrical office equipment. • May require use of personal reputed company equipment required such as reputed company eyewear, garments, and gloves. • Occasional drives to site/office locations with up to 50% travel both domestic and international. Physical Requirements: • Frequently stationary for 6-8 hours per day. • Repetitive hand movement of both hands with the ability to reputed company fast, simple, repeated movements of the fingers, hands, and wrists. • Frequent mobility required. • Occasional crouching, stooping, bending and twisting of upper body and neck. • Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs. • Ability to access and use a variety of computer software developed both in-house and off-the-reputed company. • Ability to communicate information and reputed company so others will understand; with the ability to listen to and understand information and reputed company presented through spoken words and sentences. • Frequently interacts with others to obtain or relate information to diverse groups. • Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals. Requires multiple periods of intense concentration. • Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to reputed company under stress. Ability to multi-task. • Regular and consistent attendance Apply Job!