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Senior Associate, Pricing and Market Access

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Parexel

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Location:
United Kingdom , London

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Category:
Consulting

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Contract Type:
Not provided

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Salary:

Not provided
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Job Description:

As part of Parexel Consulting, you will play a vital role in helping biopharmaceutical and medical device companies navigate the complex and ever-changing regulatory landscape. Drawing on your scientific, technical, and regulatory expertise, you will work closely with clients to develop and implement regulatory strategies that bring their products to market faster and keep them there. We value collaboration, innovation, and continuous learning. As a member of our team, you will partner with a diverse group of clients, and be exposed to various product types and therapeutic areas. You will also develop your skills through challenging assignments and mentorship from experienced regulatory professionals. Plus, you will enjoy the flexibility of working remotely while still being part of a supportive and dynamic team.

Job Responsibility:

  • Deliver high-quality, timely outputs that integrate scientific evidence, payer insights, and strategic thinking to address client objectives
  • Structure and execute defined workstreams, by breaking down complex problems into clear logical components
  • Conduct targeted primary research and secondary desk research to inform the development of strategic recommendations, ensuring alignment with client goals
  • Gather, assess, and document complex data sets and qualitative research, maintaining meticulous records of collected information
  • Identify, synthesize and interpret qualitative and quantitative evidence (i.e. clinical, economic, and real-world evidence) translating findings into clear and actionable insights and payer-relevant narratives that articulate a product's value
  • Demonstrate proficiency in utilizing all available resources effectively, striving to produce client-ready deliverables with first-time accuracy and quality, including, but not limited to: PowerPoint deliverables that are logically structured with clear messaging/takeaways
  • Word document deliverables, such as Global value dossiers (GVDs), Academy of Managed Care Pharmacy (AMCP) dossiers, and health technology assessment (HTA) submissions
  • ensuring accuracy, consistency, and relevance
  • Ensure accuracy, consistency, and attention to detail across all outputs
  • Manage assigned tasks effectively to meet deadlines, proactively communicating risks or challenges
  • Fulfill basic job-related responsibilities, including timely completion of core responsibilities and maintain compliance with all company processes, systems, and training requirements, including: timesheets, timely completion of training, documentation and archiving of project deliverables, and participation in internal initiatives or mentorship programs as requested by management
  • Demonstrate professionalism and integrity in all interactions with clients and internal stakeholders within Parexel, building credibility and trust
  • Demonstrate the ability to work in a cross-cultural environment through day-to-day interactions across different functions
  • Act as a positive and collaborative team member, supporting a high-performance, feedback-driven culture

Requirements:

  • Good / Sound Understanding of the pharmaceutical industry, healthcare systems, or market access principles is advantageous
  • Exposure and/or experience in areas such as pricing, reimbursement, market access, HTAs, and/or health economics and outcomes research (HEOR) will provide a strong foundation for the role
  • Exceptional interpersonal, verbal, and written communication skills, with the ability to convey complex technical information clearly and effectively
  • High degree of written accuracy and attention to detail, ensuring precision in all deliverables with a 'right first time' mindset
  • Proficiency in English
  • fluency in another language is an asset
  • Strong analytical skills, with the ability to interpret and synthesize diverse data sources effectively
  • Client-focused approach to work, demonstrating active listening and responsiveness to client needs
  • Proactive problem-solving mindset with ability to identify challenges and propose improvements
  • Flexible attitude towards work assignments and a willingness to embrace new learning opportunities, changing project needs and/or priorities
  • Self-motivated, enthusiastic, ambitious, and adaptable, with a keen interest in medical research, healthcare provision, and the pharmaceutical industry
  • Takes responsibility for assigned work and delivering high-quality work within agreed timelines, demonstrating initiative and accountability with appropriate guidance
  • Proactive, reliable, and responsive in a fast-paced environment
  • Positive attitude towards work, maintaining tact and respect in interactions with project teams, clients, and peers
  • Receptive to development feedback, applying insights to enhance project outcomes
  • Engages in two-way dialogue, sharing information and collaborating effectively with others on projects and initiatives
  • Strong computing skills, particularly in MS Office applications (Excel, PowerPoint, Word), literature databases (PubMed, Embase), reference management tools (EndNote) and AI tools (Co-Pilot, ChatGPT)
  • Minimum of a bachelor's degree in a scientific discipline
  • an advanced degree is preferred (e.g. MSc, PhD)
  • Strong academic track record demonstrating analytical capability and intellectual curiosity

Nice to have:

  • fluency in another language is an asset
  • advanced degree is preferred (e.g. MSc, PhD)
What we offer:
  • flexibility of working remotely
  • supportive and dynamic team
  • challenging assignments
  • mentorship from experienced regulatory professionals
  • flexible work arrangements
  • opportunities for career growth
  • diverse and global client exposure
  • learn from experts

Additional Information:

Job Posted:
May 04, 2026

Employment Type:
Fulltime
Work Type:
Remote work
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