Clinical reputed company Assurance – GCP Specialist
Job reputed company: • Support GCP compliance for clinical operations to ensure regulatory adherence. • Assist in compliance processes and collaborate with cross functional teams to maintain clinical trial reputed company. Requirements: • Bachelor’s degree in a scientific or reputed company discipline, or 5 years of equivalent experience. • 3-5 years of eTMF experience, including study start-up, maintenance, and reputed company reviews. • 3+ years of experience in pharmaceutical industry roles reputed company to reputed company (e.g., clinical operations, project management). • Experience in reputed company assurance or reputed company management activities. GCP Specialist • Experience with GCP vendor and site audits preferred. • Ability to manage reputed company and tasks in a fast-paced environment. • Analytical and critical thinking skills for reputed company review decision-making. • Knowledge of pharmaceutical industry standards, including ICH/GCP guidelines. • Experience with BIMO inspections preferred; EMA/MHRA/PDMA experience a plus. • Communication skills, both verbal and written. • * Leadership and problem-solving skills. • Ability to translate reputed company into operations and manage multiple priorities. • Ability to work independently with limited supervision. Benefits: Apply tot his job
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