Investigator Contract Lead- FSP

Parexel

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profile Job Location:

Beijing - China

profile Monthly Salary: Not Disclosed
Posted on: 17 hours ago
Vacancies: 1 Vacancy

Job Summary

When our values align theres no limit to what we can achieve.

At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us no matter what we do at Parexel contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally we do it with empathy and were committed to making a difference.

Key Accountabilities:

SCL Tasks:

  • 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.
  • Advice 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.

Skills:

  • Possess strong diplomacy leadership skills and excellent organizational ability.
  • Excellent interpersonal verbal and written communication skills.
  • Ability to motivate both individuals and a team with strong influencing skills.
  • Ability to successfully work in a virtual multicultural team environment and across different time zones different time zones.
  • Must have strong analytical skills with the ability to create or interpret legal language and budgets.
  • Demonstrate thought leadership and innovation.
  • Maintain grace under pressure while displaying a high level of professionalism.
  • Align internal and external resources to achieve objectives.
  • Demonstrated attention to detail.
  • Comprehend and interpret contract language.
  • Identify problems independently and execute solutions.
  • Quickly comprehend desired end-result goal or objective and act to accomplish
  • Demonstrated effective decision-making.
  • Solid working proficiency of all MS Office Products specifically Excel Word and PowerPoint.
  • Polished presentation skills.
  • Strong negotiation skills and ability to manage complex contracts.
  • Good project management skills and ability to manage multiple projects simultaneously.
  • Relationship-building skills.
  • Familiarity with relevant legal framework and regulations related to site contracting within the CRO industry.
  • Experience with relevant software tools and technologies used in site contracting such as eTMF and contract management systems.

Knowledge and Experience:

  • Site Contract Lead requires 3 to 5 years of experience in site contracting or combination with a related field within the CRO industry.

Education:

  • Bachelors degree in a related field (e.g. law economics business social sciences) equivalent training or industry experience.

When our values align theres no limit to what we can achieve.At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a deep conviction in...
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About Company

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Parexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our the ... View more

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