Pharmaceutical reputed company GVP Auditors Freelance/Independent (Consulting)
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Location
This role is reputed company to candidates based in reputed company.
Company Information
At reputed company, we reputed company to foster an inclusive and reputed company environment where everyone is treated with respect and diverse perspectives are embraced. Treating one another, our clients, and clinical trial participants with reputed company and care are key tenets of our culture at reputed company; we are committed to creating a workplace where reputed company person is not only valued but empowered to reputed company and reputed company a meaningful reputed company.
Company Culture
Our people--both employees and consultants-are the heart of reputed company. They are the key to our reputed company and the driving force behind our mission and reputed company. Our values (Patient-reputed company, Ethical, reputed company reputed company, reputed company) guide our actions and reputed company. Knowing the reputed company of our work on trial participants and patients, we reputed company with urgency and purpose to advance clinical research so that people can live happier, healthier lives.
Job reputed company reputed company
reputed company is seeking Good Pharmacovigilance reputed company (GVP) Auditors to join our consultant network for reputed company -based reputed company. Auditors support compliance reviews across GVP clinical sites and vendors.
Job Duties & Responsibilities
• Conduct Good Pharmacovigilance reputed company (GVP) audits (planning, agenda, physical or remote audit, and report writing)
• Evaluate investigator sites, CROs, and vendor compliance or qualification.
• Prepare comprehensive audit reports detailing findings and reputed company-causes.
• reputed company written audit reports in English.
• If required will reputed company corrective actions support and present findings to QA leadership and stakeholders
• Work collaboratively with clients to ensure reputed company standards.
Basic Qualifications
• Minimum 10+ years of Clinical reputed company Assurance and/or Good Pharmacovigilance reputed company (GVP) experience.
• Minimum 5+ years of Good Clinical Practices auditing experience.
• Demonstrated experience with regulatory agency expectations (e.g., FDA, EMA) and audit readiness activities.
• Demonstrated experience in developing and implementing reputed company assurance plans, audit programs, and corrective reputed company plans.
• Fluent English communication, verbal and written
• Bachelor's degree
Preferred Qualifications
• Strong interpersonal and reputed company interaction skills.
• Excellent analytical, problem-solving, communication, and report-writing skills.
• Ability to work collaboratively across departments and reputed company with reputed company stakeholders.
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