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Parexel

End-to-end clinical trials and regulatory consulting

Early Phase Clinical Pharmacology Solution Consultant

Pre-Sales Solution EngineeringConfirmed live in the last 24 hours
Full-time$105k - $130k

About the Job

Requirements

  • A bachelor's degree in life sciences, business, or a related field is required.
  • Three to five years of Early Phase Clinical Trials experience is required.
  • Significant experience in strategic drug development planning or involvement in planning clinical, technical, or operational strategies is required.
  • A strong understanding of clinical trial processes, regulatory requirements, and the drug development lifecycle is required.
  • Strong communication, organization, and problem-solving skills, with demonstrated ability to influence and persuade stakeholders, are required.
  • An energetic, make-it-happen attitude and ability to thrive in a complex, matrix environment and build strong cross-functional relationships are expected.
  • Strategic thinking combined with pragmatic delivery approaches, the ability to see the big picture, and attention to detail are expected.
  • Interpersonal, verbal, and written communication skills to engage effectively with business levels from peers to C-suite and project teams are expected.
  • Strong understanding of the commercial ecosystem and awareness of industry trends in the area of expertise, demonstrated through active participation in leading industry forums and professional organizations, are expected.
  • Ability to communicate complex ideas simply and compellingly to diverse audiences is expected.
  • Analytical and problem-solving skills, ability to manage multiple varied tasks, and ability to prioritize workload are expected.
  • Independent thinking, flexibility toward work assignments, and commitment to developing new capabilities are expected.
  • Willingness to travel up to 30% as needed to support client relationships and business development activities is required.

Responsibilities

  • Identify, qualify, and prioritize sales opportunities in partnership with Enterprise Accounts, Growth Accounts, and Strategic Business Units, and craft solutions tailored to client needs and Early Phase Clinical Trials sales campaigns.
  • Develop customer-focused proposal content that differentiates Parexel, articulates its value proposition, and supports business growth across multiple service lines.
  • Provide strategic advice and guidance to sponsors and internal teams, using expertise in therapeutic, technical, or functional areas to develop competitive solution models and communicate with organizational stakeholders.
  • Define bid pursuit strategy and content, review and integrate considerations into requests for proposal responses, and participate in bid pursuit meetings to align with client objectives and Parexel capabilities.
  • Maintain knowledge of relevant products, pipelines, and market trends; identify business opportunities and use a consultative approach to position Parexel as an industry leader.
  • Support clients through the pre-award process, promote solution adoption, solve complex business issues, and present strategic recommendations to client leadership.
  • Bring market requirements and client feedback into Product Management and solution development to create relevant, competitive value propositions.

Desired Qualifications

  • An advanced degree (MBA, MS, or equivalent) in business, life sciences, or a related field is preferred.
  • Experience in a specific therapeutic area or clinical development specialty is preferred.
  • Active participation in industry forums, professional organizations, or thought leadership activities is preferred.
  • Experience with clinical trial management systems, proposal development platforms, or enterprise software solutions is preferred.

About the Company

Parexel

End-to-end clinical trials and regulatory consulting

Parexel provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device clients from Phase I to Phase IV. Its offerings include clinical trial management, regulatory consulting, and biostatistical analysis to support the design, execution, and analysis of clinical studies. The company operates as a CRO, partnering with sponsors to manage trials, ensure regulatory compliance, and generate robust data for drug development. What sets Parexel apart is its breadth of services across the trial lifecycle, emphasis on quality and reliability, and industry recognition, along with a focus on patient-centric approaches and leadership in gender partnership. The company’s goal is to help clients bring new therapies to market efficiently and safely by delivering high-quality, compliant trial outcomes and data that support regulatory submissions.

Company size
10,001+
Company stage
Acquired
Total funding
$8.5B
Headquarters
Durham, NC
Founded
1982

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