FSP Top Global Pharma
Mainly responsible for developing investigator budget for Asia-pacific region

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

61Receives 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.
61Reviews 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.
61Develops the detailed investigator grant budget estimates and supporting documents with assistance from Clinical Operations according to protocol specifications through currently available software package/resources.
61Ensures Investigator Grants are in agreement with RFP, client specifications and communications, and internal assumptions.
61Collaborates with team members, operations and business development, to ensure Grants estimates are appropriate for the study.
61Validates investigator grant estimates against available internal and external benchmarking data.
61Tracks and measures progress through collection of cycle time metrics and other quality key performance indicators (KPIs).
61Updates proposals tools, systems and/or forms regarding proposal or rebid status and Investigator Grants value as directed.
61Researches, compiles, and creates necessary information as required in support of generation of Investigator Grants.
61Escalates issues/concerns to department leadership.

QUALIFICATION REQUIREMENTS

61BA/BS degree or equivalent in a health related field, or equivalent combination of education and experience; includign generating investigator grant estimates.
61Clinical 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.
61Intermediate proficiency in Microsoft Office Suite (Word, Excel, and PowerPoint), email, and voicemail.
61Above-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.