Study Grant Analyst II

🔥 1 minute ago

🇮🇳 India – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧐 Analyst

👻 Ghost score 10%

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Parexel

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1983

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 Venture Round on 1990-01

Consulting • Healthcare • Logistics

Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.

📋 Description

• Prepare accurate and competitive Clinical Study grants for Phase I–IV studies across all clinical indications using Clinical Study Pricing Tools, including Grant Plan • Collaborate with Proposal team members to prepare budget concepts for pre-sales proposals while complying with RFP requirements and Parexel policies • Lead creation, revision, escalation, and approval of Clinical Study grants for awarded projects with Site Contracts Leaders, Study Project Leaders, and Project Directors • Prepare post-award Clinical Study grant analyses • Participate in strategy sessions and budget reviews to develop win themes, assess competitor benchmarks, and discuss client needs • Ensure Clinical Study grant information complies with Fair Market Value principles and the Physician Payments Sunshine Act • Share lessons learned and new scenarios with the team • Deliver and maintain client-focused grants analysis to measure performance and proactively identify issues • Support and build departmental or functional training plans, content, and delivery • Maintain compliance with applicable guidelines, regulatory requirements, and Parexel SOPs • Participate in systems and standards improvement activities, committees, and task forces, including change management • Maintain agreed productivity and billability levels • Complete administrative tasks including timesheets, training, and travel expense claims • Travel as needed and comply with applicable travel and billability guidelines • Build partnerships, model teamwork, and maintain a positive, results-oriented work environment • Implement process improvements in response to client and team feedback and quality audits • Encourage teamwork, quality, and productivity across CRS and Parexel

🎯 Requirements

• 3–5 years’ work experience in clinical site budget development, using GrantPlan or Grant Manager, in a similar role within the managed care, pharmaceutical, or biotechnology industries • Experience using industry benchmarking databases and other tools to ensure fair market value in investigator grant development • Degree-level education in biological science, pharmacy, or another health-related discipline preferred, or equivalent nursing qualification or relevant clinical equivalent experience • Strategic thinking and proactive, solutions-based approach • Excellent analytical and problem-solving skills • Strong cross-functional and upward communication skills • Client-focused approach and ability to build and maintain client trust • Ability to resolve issues independently and escalate appropriately • Familiarity with standard business and eClinical systems used in clinical research • Proficiency in Microsoft Excel, PowerPoint, and Word • Ability to become proficient with Parexel systems • Ability to manage multiple projects and prioritize workload with attention to detail • Outstanding negotiation, influencing, and organizational skills • Demonstrable stakeholder and relationship management experience • Ability to assess business implications and customer impact • Ability to make and execute difficult decisions • Ability to work successfully in a virtual team environment • Working knowledge of ICH Guidelines, Good Clinical Practices, regulatory agency requirements, and Parexel SOPs • Familiarity with healthcare compliance guidance including HIPAA, FCPA, and Safe Harbor