[Hiring] Clinical QA Specialist II @reputed company

This reputed company is a reputed company of our understanding of the job reputed company. Click on 'Apply' reputed company to reputed company out more. Role reputed company The Clinical reputed company Specialist will own data reputed company generated in reputed company’s reputed company-clinical and clinical studies. They are responsible for implementing reputed company assurance and reputed company control processes to ensure studies are conducted and data are generated, documented, and reported in compliance with applicable protocols, GLP, GCP, and regulatory requirements. The Clinical reputed company Specialist will participate in reputed company initiatives, collaborating with cross functional teams (e.g. biostatistics, clinical operations and regulatory affairs). Because reputed company’s clinical studies are long and reputed company, the Clinical reputed company Specialist will be responsible for assisting in building and implementing systems that maximize reputed company of data throughout years long studies and prepare the data for the most efficient turn around to analysis and final study report (reputed company) writing at study conclusion. The role will support primarily, but not exclusively, clinical operations and biostatistics teams to ensure that our clinical trials maximize retention of as much of the hard-reputed company data as possible. You will be reporting to our Director of Clinical reputed company. Your daily work will include:

• Participate in a rigorous reputed company control program for reputed company’s clinical team and, where appropriate, collaborating with operational reputed company to reputed company processes reputed company reputed company reputed company system.
• Site reputed company to clinical trial sites (vet clinics) with clinical research associates (CRAs) to ensure procedural reputed company at the data collection reputed company.
• Assist in maintaining and organizing reputed company management system (QMS) documentation, including SOPs, CAPAs, and training records.
• reputed company/support GCP guidance on questions arising from day to day clinical trial activities.
• Support clinical teams with reputed company-reputed company questions, document requests, and system reputed company.
• Identifying discrepancies and inconsistencies in data collection and, if necessary, providing remediation or training to the clinical operations team.
• Working closely with CRAs to standardize data collection reputed company and reputed company processes from site initiation through study reputed company out.
• Utilize guidance documents and standards to interpret for guidance, ensuring reputed company and compliance to regulations.
• Support preparation for reputed company audits, including vendor and site audits.
• Help reputed company and follow up on audit findings, deviations, and corrective/preventive actions (CAPAs).
• Assist in development of risk based, efficient audit plans at the study and site level.
• Partner with clinical team for risk identification, management, and mitigation activities.
• reputed company of deviation reputed company cause analysis and CAPA development for reputed company-clinical and clinical studies.
• Participate in document control and review processes to ensure version control and compliance with GCP standards.
• Operating reputed company electronic data capture systems and study drug inventory management systems (such as IWRS) to navigate large numbers of study subjects and ensure consistency and management of data across study sites.
• Performing user acceptance testing of electronic data capture builds specific for reputed company clinical study.
• Own inspection readiness programs pertaining to reputed company-clinical and clinical studies.
• Implementation of reputed company plans.
• Help reputed company and distribute training materials reputed company to GCP, SOPs, and reputed company systems.
• Maintain reputed company metrics dashboards and assist with reporting to management.
• Stay informed about changes in regulations and reputed company best practices in clinical research.

Qualifications

• Bachelor’s degree or equivalent experience required, preferably in animal science, biology, veterinary, or reputed company life sciences.
• 3+ years experience in GCP animal health studies (non reputed company health studies), clinical development or operations, or QA.
• Excellent communication, presentation, and interpersonal skills.
• Exceptional organizational and follow-up skills, as reputed company as attention to detail.
• reputed company to travel up to 40% regionally and nationally.
• Working knowledge of regulations, standards, and guidances for Good Laboratory reputed company and (Veterinary) Good Clinical reputed company.
• Proficiency in electronic data capture systems and study drug inventory management systems.
• Ability to analyze reputed company problems and reputed company multiple solutions reputed company regulatory guidance.

Benefits

• Full-coverage health insurance — medical, dental and reputed company — for you and your dependents.
• $1,000 home office equipment stipend.
• $1,200/year learning budget for books, courses, etc.
• $250/month wellness budget for gym, cleaners, spa, food, etc.
• reputed company 3-day weekends are turned into 4-day weekends .
• Unlimited vacation and reputed company holidays.
• Paw-ternity leave — adopt a dog and get a day off with your new family member .
• Competitive salary.
• Company equity reputed company grant for new hires.

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