When our values align, there's no limit to what we can achieve. The Site Contracts Lead is responsible for overseeing the site contracting process for clinical trials.
The Site Contracts Lead will manage the site contracting process in a way to streamline negotiations, control budgets, manage risks, and ensure that all parties, both external and internal, involved in the contracting process are aligned and working toward the same goals.- at least 5-7 years or more in experience related to site contracting or combination with a related filed/ roles within CRO industry is required.- regional/ global lead experience is highly preferred.- extensive experience in both initial/ amendment contracts/ agreement is needed for candidate's local country.
(other country experience is highly preferred)- great communication skill in English and candidates' local language Please refer below Key Accountabilities of Site Contracts Lead Oversee the site contracting process for clinical trials, ensuring that contracts are executed in a timely and effective manner Monitor, drive, and report on site contract performance throughout the whole lifecycle, specifically metrics such as contract cycle times, contract aging time, contract quality and tracking compliance Developing all Project set up documents for contracting, including but not limited to: CTA templates, Fallback languages, Site Contract Plan, etc.
Advise on investigator grant budgets/parameters in collaboration with a global team of Grant Strategy and Investigator fees Ensuring that all terms and conditions are clear, effectively aligned with the overall project needs Participate on KOMs to provide feedback on preferable contracting strategies and beneficial tactics Oversee project specific Site Contracts team, providing leadership, guidance, and necessary project/client specific training to the team members Develop and implement best practices for site contract management, including specific processes, procedures, and tools May support the department through shared knowledge and other defined pathways, as well as deescalate issues Conscientiously control the budget from a site contracting aspect, ensuring that costs are tracked, managed, and communicated timely and effectively. Identify and mitigate risks associated with the site contracting process, including risks related to timelines, costs, effectiveness of implemented strategy, and quality.
Collaborate with all relevant stakeholders until resolution. Maintain frequent, clear and effective communication with all stakeholders involved with or dependent upon the site contracting process, including sponsors, key internal stakeholders, vendors, collaborative CROs and sites (as applicable) Build and maintain strong working relationships with external and internal stakeholders, and facilitate alignment of relevant parties aiming at expedited contract execution Provide necessary support to cross-functional teams including Start up, Global Clinical Operations, Investigator Payments, Business Development and Feasibility Provide regular updates and reports on the site contracting process to clients, senior management and other stakeholders as needed Monitor data accuracy and completeness Support Project Lead with implementation of project hour forecasting for Site Contracts team to ensure accurate planning, resource allocation and budgeting throughout trial lifecycle
Free
Site Contracts Lead, Taiwan
Taiwan, Taiwan, Taiwan,
發表 October 25, 2024
描述
聯繫雇主
雇主信息
PAREXEL International is a leading global biopharmaceutical services provider, which continues to be a premier, trusted partner to clients who rely on the Company for expertise and flexibility, as well as the efficiencies of a worldwide infrastructure, to help them more quickly achieve their development and commercialization goals. For 30 years, PAREXEL has complemented client organizations with strategic insight, deep scientific knowledge, tactical expertise, and a wealth of experience throughout the development process. The Company's offerings include worldwide regulatory expertise, Phase I-IV clinical research services, eClinical technologies that accelerate development, and integrated commercialization services. PAREXEL is focused on providing tailored solutions that match a client's specific needs by applying the right blend of resources and capabilities, as well as the right guidance and high level of quality needed to help them bring safe and effective treatments to patients sooner.
Headquartered near Boston, Massachusetts, PAREXEL operates in over 70 locations throughout more than 50 countries, and has over 11,000 employees worldwide.
Visit www.PAREXEL.com for more information.
Specialties
Regulatory and product development consulting,
early phase clinical research,
phase II-III clinical research,
late phase clinical research,
eClinical solutions,
patient and site recruitment,
clinical logistics,
flexible outsourcing models,
strategic partnering