Job Responsibilities:

• Administer HR processes, including onboarding, offboarding, employee records, benefits, and compensation
• Respond to employee and manager inquiries regarding HR policies, systems, and procedures
• Monitor HR systems for data accuracy and troubleshoot discrepancies
• Conduct root cause analysis and recommend corrective actions for operational issues
• Support compliance with GDPR, SOX, and local employment regulations
• Support international HR operations, such as employment eligibility, visa/immigration processes, and relocation assignments
• Assist in updating SOPs and process documentation
• Collaborate with HR Centers of Excellence and HRBPs to support program execution
• Analyze HR processes and systems, providing recommendations and corrective action plans to improve efficiency, compliance, and employee experience
• Participate in People Operations projects and contribute to continuous improvement initiatives
• Provide guidance and support to junior People Operations team members

Requirements:

• Bachelor's degree in Human Resources, Business Administration, or related field
• 3-5 years of experience in shared services and working in a global/regional environment
• Familiarity with global, country, and/or local employment law and regulations
• Proven ability to work in a collaborative, cross-functional environment
• Proficiency in HRIS systems (e.g., Workday, Service Now) and Microsoft Office
• Excellent communication, data analytical, and organizational skills
• Ability to work independently and manage multiple priorities

Job Data by YubHub.

The Clinical Research Associate (CRA) II - Sponsor dedicated - Argentina will perform site qualification, site initiation, interim monitoring, site management activities and close-out visits. The CRA II will ensure regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance.

Responsibilities:

• Perform site qualification, site initiation, interim monitoring, site management activities and close-out visits
• Evaluate overall performance of site and site staff and provide recommendations regarding site-specific actions
• Verify the process of obtaining informed consent has been adequately performed and documented for each subject/patient
• Assess factors that might affect subject/patient's safety and clinical data integrity at an investigator/physician site
• Conduct Source Document Review of appropriate site source documents and medical records
• Verify required clinical data entered in the case report form (CRF) is accurate and complete
• Apply query resolution techniques remotely and on site, and provide guidance to site staff as necessary
• Utilize available hardware and software to support the effective conduct of the clinical study data review and capture
• May perform investigational product (IP) inventory, reconciliation and reviews storage and security
• Routinely review the Investigator Site File (ISF) for accuracy, timeliness and completeness
• Document activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents
• Support subject/patient recruitment, retention and awareness strategies
• Enter data into tracking systems as required to track all observations, ongoing status and assigned action items to resolution
• Prepare for and attend Investigator Meetings and/or sponsor face to face meetings
• Provide guidance at the site and project level towards audit readiness standards and support preparation for audit and required follow-up actions

Qualifications:

• Bachelor's degree or RN in a related field or equivalent combination of education, training and experience
• Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements
• Good computer skills and ability to embrace new technologies
• Excellent communication, presentation and interpersonal skills
• Ability to manage required travel of up to 75% on a regular basis

Job Data by YubHub.

Responsibilities:

• Perform site qualification, site initiation, interim monitoring, site management activities, and close-out visits
• Evaluate overall performance of site and site staff and provide recommendations regarding site-specific actions
• Verify process of obtaining informed consent has been adequately performed and documented for each subject/patient
• Assess factors that might affect subject/patient's safety and clinical data integrity at an investigator/physician site
• Conduct Source Document Review of appropriate site source documents and medical records
• Verify required clinical data entered in the case report form (CRF) is accurate and complete
• Apply query resolution techniques remotely and on site, and provide guidance to site staff as necessary
• Utilize available hardware and software to support the effective conduct of the clinical study data review and capture
• Verify site compliance with electronic data capture requirements
• Perform investigational product (IP) inventory, reconciliation, and reviews storage and security
• Routinely review the Investigator Site File (ISF) for accuracy, timeliness, and completeness
• Document activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents
• Support subject/patient recruitment, retention, and awareness strategies
• Enter data into tracking systems as required to track all observations, ongoing status, and assigned action items to resolution
• Understand project scope, budgets, and timelines; manage site-level activities/communication to ensure project objectives, deliverables, and timelines are met
• Act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate
• Prepare for and attend Investigator Meetings and/or sponsor face-to-face meetings
• Provide guidance at the site and project level towards audit readiness standards and support preparation for audit and required follow-up actions

Qualifications:

• Bachelor's degree or RN in a related field or equivalent combination of education, training, and experience
• Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements
• Good computer skills and ability to embrace new technologies
• Excellent communication, presentation, and interpersonal skills
• Ability to manage required travel of up to 75% on a regular basis

Job Data by YubHub.