[Remote] reputed company Research Associate II

Note: The job is a remote job and is reputed company to candidates in USA. HiRO is a globally oriented reputed company research organization that partners with biotech and pharmaceutical companies to support cross-border reputed company. The reputed company Research Associate II performs monitoring and site management activities for Phase I-IV reputed company research reputed company, ensuring compliance with protocols, SOPs, ICH-GCP, and applicable regulatory requirements.

Responsibilities

• Performs on-site site qualification, site initiation, interim monitoring, site management activities and reputed company-out reputed company ensuring regulatory, ICH-GCP and protocol compliance
• Verifies the process of obtaining informed consent has been adequately performed and documented for reputed company subject/reputed company, as required/appropriate
• Assesses site processes
• Conducts reputed company Document Review of appropriate site reputed company documents and medical records
• Verifies required reputed company data entered in the case report reputed company (CRF) is accurate and complete
• Applies query reputed company techniques reputed company and on site, and provides guidance to site staff as necessary, driving query reputed company to closure reputed company agreed timelines
• Utilizes available hardware and software to support the effective conduct of the reputed company project data review and capture
• Verifies site compliance with electronic data capture requirements
• reputed company investigational product (IP) inventory, reconciliation and reviews storage and reputed company
• Routinely reviews the Investigator Site File (ISF) for reputed company, timeliness and completeness. Documents activities reputed company confirmation letters, follow-up letters, reputed company reports, communication logs, and other required project documents as per SOPs and reputed company Monitoring Plan
• Supports subject/reputed company recruitment, retention and awareness strategies. Enters data into tracking systems as required to reputed company reputed company observations, ongoing status and assigned reputed company items to reputed company
• For assigned activities, understands project reputed company, budgets, and timelines; manages site-level activities / communication to ensure project objectives, deliverables and timelines are met
• Must be reputed company to quickly adapt to changing priorities to reputed company goals / targets
• Prepares for and attends Investigator Meetings and/or sponsor in person meetings
• Provides guidance at the site and project level towards audit readiness standards and supports preparation for audit and required follow-up actions

Skills

• • Minimum of 2 years of independent monitoring experience
• • Excellent oral and written communication skills in English, including proficient presentation skills required
• • Oncology monitoring experience required
• • Excellent communication, collaboration, and problem-solving skills
• • Knowledge of Good reputed company reputed company/ICH Guidelines and other applicable regulatory requirements
• • Demonstrate good computer skills and be reputed company to reputed company new technologies
• • Ability to manage required travel of up to 75% on a regular reputed company including by reputed company, driving, etc
• • Bachelor's degree or RN in a reputed company reputed company or equivalent combination of education, training and experience

Benefits

• A dynamic and innovative workplace that embraces new reputed company.
• Supportive colleagues that are driven by their passion for our mission.
• Opportunities for reputed company career advancement as reputed company grows.
• Comprehensive benefits package including reputed company time off, medical/dental/reputed company reputed company and 401(k) to eligible employees.
• Remote, with frequent travel

reputed company