Senior Study Grant Analyst

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.

The Senior Study Grant Analyst position in the Grants Strategy Team (GST) within Launch Excellence department is a highly varied and challenging role suitable for an individual with both in-depth business operational process experience global understanding of healthcare compliance expertise in the development of Clinical Site budget and grants and aptitude for technology optimization and implementation.

The role is accountable for Grants estimates delivery of their respective portfolio of client partners and ensuring alignment to delivery of commitments within the agreed expectations including alignment to operational processes. Leverage actual PXL portfolio data for a more comprehensive view of FMV to improve client risk reviews and approval processes.

The role is an experienced leader responsible for liaising with senior levels of management and the ability to work with leaders within other core delivery functions. The role provides the overall strategy and leadership for Study Grants of large complex clinical trials or clinical trial programs.

The role monitors and evaluate the industry changes in policy and technologies that impact Grants Strategy to ensure the highest standard of delivery to the client. The role will own project(s) or program(s) reporting within a portfolio to assess trends ensure mitigations are effective and to develop Grants Strategy delivery KPIs for overall client satisfaction.

Key Accountabilities:

Build Grant Estimate

• Grants estimates delivery of respective portfolio of client partners and ensuring alignment to delivery of commitments within the agreed expectations including alignment to operational processes.
• Augmented clinical expertise to define & validate specifications and expectations regarding Grants build and scenario planning.
• Leverage actual PXL portfolio data for a more comprehensive view of FMV to improve client risk reviews and approval processes
• Expand Analyze & Consult contribution to leverage actual PXL portfolio data & GrantPlan / Grant Manager reports for a more comprehensive view of FMV to improve client risk reviews
• Create consultative capacity for stakeholder engagement and enhanced analytics
• Robust scenario development improved output quality and de-risked delivery
• Define business processes for consistent predictive service offering
• Subject Matter Expert oversight on the creation revision escalation and approval process of Clinical Study grants for pre award & awarded Projects.
• Participation in strategy sessions and budget reviews when requested to develop win themes identify and assess competitors benchmarks and discuss client needs.
• Ensure that all Clinical Study grant information is performed in full compliance with Fair Market Value (FMV) principles and the Physician Payments Sunshine Act.
• Expertise with healthcare compliance and other relevant guidance (HIPAA FCPA Safe Harbor etc.)
• Display good knowledge sharing capabilities share lessons learned and new scenarios with the team.
• Deliver and maintain client-focused Grants analysis to measure performance and proactively identify issues for resolution
• Support & build departmental or functional training plans content & delivery
• Study Grant Tool Vendor Management Contact expectation management KPIs Governance Meeting agenda and conduct reduced downtimes and ensuring business continuity.

General Administration & Operations

• Maintain a working knowledge of and assure compliance with applicable ICH Guidelines Good Clinical Practices Regulatory Agency requirements and Parexel SOPs
• Participate in Parexel and department system/standards improvement activities or committees task force groups as needed including change management
• Ensure agreed levels of productivity/billability are maintained
• Complete routine administrative tasks in a timely manner (e.g. timesheets training travel expense claims). Ensure compliance with travel and billability guidelines for department region or function are met where appropriate.
• Travel as needed.
• Maintain a positive results orientated work environment building partnerships and modeling teamwork communicating to the team in an open balanced and objective manner
• Ensure implementation of process improvements in response to client and team feedback and quality audits
• Look within and beyond CRS to encourage teamwork quality and productivity efforts to the benefit of CRS and PAREXEL

Skills:

• Strategic Thinking skills that support the ability to create a sense of urgency and take a proactive solutions-based approach
• Excellent analytical and problem-solving skills to define and resolve issues in a variety of complex situations
• Leverage communication across boundaries and uses multiple communication mechanisms to convey information across functional lines and upward within Parexel.
• Client focused and demonstrated ability to create and maintain trust with the client through project and personal interactions; act as a trusted advisor and become involved in the clients decision-making process.
• Ability to resolve issues independently and knows when to call on senior management for involvement in communicating to external & internal customers after assessing the organizational implications of the interaction and consultation with Senior Management.
• Familiarity with standard business and eClinical systems used in Clinical Research
• Proficient in Microsoft Excel Power Point and Word software
• Ability to become proficient with Parexel systems
• Advanced ability to successfully manage a full workload across multiple and varied projects/tasks with enthusiasm and prioritize workload with attention to detail
• Outstanding negotiation influencing and organizational skills
• Demonstrable experience of stakeholder/relationship management with a client focused approach to work.
• Able to understand the business implications of decisions and impact on customer
• An ability to assess situations and make and carry through difficult decision
• Ability to successfully work in a (virtual) team environment

Knowledge and Experience:

• 5 8 years work experience in Study Grants ICD coding clinical site budget development (use of GrantPlan or Grant Manager) in a similar role within the managed care pharmaceutical or bio-technology industries.
• Experience in the use of industry benchmarking databases and other tools utilized to ensure fair market value in the development of investigator grants

Education:

• Educated to Postgraduate / degree level (biological science pharmacy or other health-related discipline preferred) or equivalent nursing qualification or relevant clinical other equivalent experience