www.bhdu.cn-夜肉伦伦影院无码 ,国产精品www夜色视频,3d动漫精品啪啪一区二区免费,久久婷婷综合缴情亚洲狠狠

JOB SUMMARY

Develops domestic and global investigator grants estimates based on review of Request for Proposals (RFPs)/protocol/synopsis information in support of proposals for simple to moderately complex protocols. Collaborates with team members, operations and business development, to develop grant estimates.

JOB RESPONSIBILITIES

?Receives and analyzes RFPs documents with particular focus on protocol/synopsis details as they relate to determination of anticipated investigational study site and subject reimbursement costs.
?Reviews and extracts details from RFP documents (clinical trial protocols/synopsis) related to site performed study activities and applies these to detailed investigator grant estimates, with assistance from proposal management staff when needed.
?Develops the detailed investigator grant budget estimates and supporting documents with assistance from Clinical Operations according to protocol specifications through currently available software package/resources.
?Ensures Investigator Grants are in agreement with RFP, client specifications and communications, and internal assumptions.
?Collaborates with team members, operations and business development, to ensure Grants estimates are appropriate for the study.
?Validates investigator grant estimates against available internal and external benchmarking data.
?Tracks and measures progress through collection of cycle time metrics and other quality key performance indicators (KPIs).
?Updates proposals tools, systems and/or forms regarding proposal or rebid status and Investigator Grants value as directed.
?Researches, compiles, and creates necessary information as required in support of generation of Investigator Grants.
?Escalates issues/concerns to department leadership.

QUALIFICATION REQUIREMENTS

?BA/BS degree or equivalent in a health related field, or equivalent combination of education and experience; includign generating investigator grant estimates.
?Clinical trial expertise, experience in a healthcare related field (Study Coordinator, CRA, Nursing, healthcare administration) across multiple therapeutic areas preferred. Understanding of the clinical trial process and involvement of CROs.
?Intermediate proficiency in Microsoft Office Suite (Word, Excel, and PowerPoint), email, and voicemail.
?Above-average attention to detail, effective oral/written communication skills along with highly-developed interpersonal and strong team oriented skills. Ability to work independently to meet deadlines.