Job Description ​​​ HGR Application and Maintenance Execution: Execute HGR application activities, focusing on the preparation and submission of applications.

Collaborate with key stakeholders to ensure timely and high-quality delivery of HGR applications, addressing and communicating any issues that affect delivery.  ​HGR Submission and Data Management: Assist in the preparation and submission of HGR applications, ensuring precise online data entry and dossier preparation.  ​Document Compilation and Submission: Compile and submit all required ethics and local document packages, ensuring accuracy and adherence to compliance standards.  ​Regulatory Compliance and Approvals: Support activities necessary for obtaining HGR and sample exportation approvals, ensuring alignment with regulations.  ​Regional Collaboration: Help manage the collection of essential documents from sites, performing quality checks to ensure ALCOA compliance.  ​Data Tracking and Archiving: Maintain detailed tracking of HGR applications and approvals, ensuring thorough documentation archiving for compliance.  ​Compliance Monitoring: Monitor HGR compliance for assigned studies, resolving implementation issues with guidance from senior colleagues.  ​Cross-Functional Collaboration: Work collaboratively with key stakeholders to ensure the HGR application process aligns with project goals, focusing on effective communication and coordination.  ​Process Improvement: Identify opportunities for minor process enhancements and assist in their implementation.  ​Knowledge Enrichment: Engage in training programs to stay updated on HGR regulations and industry best practices.  Qualifications ​​​​ Educational Background: A bachelor’s degree in life sciences, medicine, pharmacy, health sciences, or a related field is required.  ​Work Experience: At least 2 years of experience in the pharmaceutical industry, preferably with exposure to human genetic resources.  ​Knowledge and Skills: Solid understanding of human genetic resource regulations, including familiarity with ICH GCP and clinical trial workflows.

Strong time management skills and attention to detail, with the ability to manage multiple tasks in a high-volume work environment.

Proficiency in data tracking and documentation processes is advantageous.  ​Communication Skills: Good communication skills to interact effectively with team members and external stakeholders, ensuring collaboration across projects.  Additional Information Abb Vie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion.  It is Abb Vie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.

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