Study Grant Analyst II
India, Remote Additional Locations: { "ID": [ { "#text": "78e2cb0c8edd1005449132ad61fb0000", "@type": "WID" }, { "#text": "2281", "@type": "Location_ID" } ], "@Descriptor": "India-Bengaluru-Remote" } Job ID R0000022213 Category AdministrativeAbout this Role
Build Grant Estimate
- Timely preparation of accurate and competitive Clinical Study grants (Phases I – IV for all clinical indications) via proficient usage of any Clinical Study Pricing Tool that PAREXEL is required to use to support our Clients’ needs. The default, currently licensed tool in this regard is Grant Plan.
- Collaborate to prepare competitive budget concepts for Pre-sales business Proposals in conjunction with other members of the Proposal team while remaining compliant with the Request for Proposal (RFP) and PAREXEL internal policies.
- Subject Matter Expert and Lead on the creation, revision, escalation, and approval process of Clinical Study grants for awarded Projects with the assigned Site Contracts Leader and Study Project Leader and Project Director, as appropriate.
- Preparation of additional Post Award Clinical Study grant analyses for the assigned Site Contracts Leader and Study Project Leader and Project Director, as appropriate.
- Participation in strategy sessions and budget reviews when requested to develop win themes, identify, and assess competitor’s 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.
- Familiarity with healthcare compliance and other relevant guidance (HIPAA, FCPA, Safe Harbor, etc.)
- Display good knowledge sharing capabilities, share lessons learnt 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
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.
- 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 GLE to encourage teamwork, quality and productivity efforts to the benefit of GLE and PAREXEL
Build Grant Estimate
- Timely preparation of accurate and competitive Clinical Study grants (Phases I – IV for all clinical indications) via proficient usage of any Clinical Study Pricing Tool that PAREXEL is required to use to support our Clients’ needs. The default, currently licensed tool in this regard is Grant Plan.
- Collaborate to prepare competitive budget concepts for Pre-sales business Proposals in conjunction with other members of the Proposal team while remaining compliant with the Request for Proposal (RFP) and PAREXEL internal policies.
- Subject Matter Expert and Lead on the creation, revision, escalation, and approval process of Clinical Study grants for awarded Projects with the assigned Site Contracts Leader and Study Project Leader and Project Director, as appropriate.
- Preparation of additional Post Award Clinical Study grant analyses for the assigned Site Contracts Leader and Study Project Leader and Project Director, as appropriate.
- Participation in strategy sessions and budget reviews when requested to develop win themes, identify, and assess competitor’s 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.
- Familiarity with healthcare compliance and other relevant guidance (HIPAA, FCPA, Safe Harbor, etc.)
- Display good knowledge sharing capabilities, share lessons learnt 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
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.
- 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 GLE to encourage teamwork, quality and productivity efforts to the benefit of GLE and PAREXEL
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