Position Summary
The Portfolio Specialist, Access Operation is responsible for support managing and optimizing a portfolio of projects across Pricing & Market Access, Evidence Evaluation. Real World Evidence, Advanced Analytics Consulting to maximize value and align with organizational strategy.The Portfolio Specialist will play a crucial role in supporting broader program management activities, ensuring smooth coordination across various workstreams, and maintaining compliance with company standards. The ideal candidate will have a strong background in life sciences and familiarity with clinical trial processes.
Key Responsibilities
Broader Program Management
- Evaluate and prioritize portfolio components based on strategic alignment, risk, and potential return
- Monitor portfolio performance and make recommendations for improvements
- Track monthly opportunities and assess off-label content
- Screen the pipeline to identify new opportunities and ensure alignment with current projects
- Track company newsletters and clinical trial pipeline information
- Maintain case studies based on completed projects in different therapy areas and organograms of the clients
Contracting and Tracking
- Support the Subject Matter Experts (SMEs) / Account Leads with contracting tasks and track their progress
Quality and Compliance Coordination
- Coordinate the review process for reports by quality leads within the Service Lines
- Conduct SOP audit spot checks
- Implement changes to SOPs, including templates and processes
- Ownership pf client feedback log: gather and action client feedback
Team Coordination
- Coordinate across the cross-Service Line teams for various indications
- Manage program coordination with the wider Parexel organization / Business Units / Service Lines
Timelines and Resource Management
- Maintain the timeline tracker updated across the portfolio and link current and future projects with resourcing.
- Leverage data and insight from ongoing projects and workstreams to identify new opportunities
Reporting and Meetings
- Prepare slides for Business Review Meetings and Quarterly Business Reviews (QBR)
Qualifications
- Bachelor’s degree in a scientific related field (e.g., Life Sciences, Pharmacy).
- Strong background in scientific writing and familiarity with clinical trials and regulatory requirements.
- Excellent organizational and time management skills.
- Strong communication skills, with the ability to work collaboratively across teams.
- Proficiency in project management tools and software.
- Detail-oriented with a strong focus on quality and compliance.
- Ability to manage multiple projects simultaneously and meet deadlines.
- Proficiency in Microsoft Office Suite, particularly Excel and PowerPoint
- Preferred previous experience in portfolio management, or a related role.
Skills And Competencies
- Attention to detail and ability to manage and track multiple projects/priorities, ensuring timely completion and adherence to quality standards.
- Communication: Strong written and verbal communication skills, with the ability to convey complex information clearly and concisely.
- Scientific Writing: Proficiency in scientific writing, with the ability to assess and evaluate off-label content.
- Compliance and Quality Management: Experience in conducting quality checks, SOP audits, and ensuring compliance with regulatory requirements.
- Team Coordination: Ability to coordinate across multiple teams and workstreams, ensuring smooth execution of program activities.
- Analytical Skills: Strong analytical skills, with the ability to conduct revenue forecast deep-dives and identify opportunities within workstreams.
Location:
Bengaluru -Office basedShift: 12 pm