Description:
Main purpose of the job:
Oversee the project planning, staff management, and site setup in compliance with sponsor and regulatory requirements The role supports scientific goals, data quality, dissemination efforts, and collaboration with international partners while ensuring smooth project execution and adherence to Good Clinical Practice (GCP) and local regulationsLocation:
Garlington Estate, Pietermaritzburg, Hilton – KwaZulu-NatalKey performance areas:
Project Planning and Oversight Plan, organize, and oversee projects to achieve operational and scientific goals, ensuring timely execution Service Provider and Resource Management Manage external service providers and resources to ensure efficient project execution Stakeholder Coordination and Collaboration Engage with international collaborators and stakeholders through regular communication and partnership Facilitate community entry, support site setup, and ensure smooth study implementation. Staff Management and Development Recruit, train, supervise, and mentor project staff while fostering continuous learning and performance improvement Regulatory Compliance and Ethical Conduct Ensure adherence to ethical guidelines, sponsor requirements, Good Clinical Practice (GCP), and local regulations Budget and Financial Management Assist in managing project finances, ensuring appropriate use of funds and financial accountability Documentation and Reporting Maintain accurate project records and ensure compliance with scientific, ethical, and financial reporting requirements Quality Assurance and Data Management Oversee data integrity, storage, and quality assurance processes to maintain protocol fidelity and compliance Publication and Dissemination Support Collaborate with the scientific team to support the dissemination of research findings through publications and presentationsRequired minimum education and training:
Masters Degree in the Social and Human Sciences or related fields Good Clinical Practice (GCP) and Human Subjects Protection (HSP) Certifications Proficiency in data management tools such as REDCapRequired minimum work experience:
At least 2 years of experience managing multi-year, complex research or clinical projects Minimum 2 years in a project manager role, supervising teams of 10+ members Demonstrated experience in protocol development, study design, and implementationDesirable additional education, work experience and personal abilities:
Experience in
12 Feb 2025;
from:
gumtree.co.za