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Parexel

End-to-end clinical trials and regulatory consulting

Senior Scientific Specialist with experience in HEOR and RWE

Technical WritingUpdated on Nov 9
Full-timeNo salary listed

About the Job

Requirements

  • Experience in Health Economics and Outcomes Research (HEOR).
  • Experience in Real-World Evidence (RWE).
  • Prior experience in a similar role within a medical communications agency.
  • Advanced scientific writing, reviewing, and editing competency.
  • Ability to rapidly acquire specialized therapy area knowledge.
  • Strong client focus and professional interpersonal skills.
  • Advanced problem-solving and project management abilities.
  • Proficiency in Microsoft Word, PowerPoint, and Excel.
  • Strong presentation and mentoring skills.
  • Ability to work effectively in a matrix environment.
  • A degree and higher degree in Life Sciences, Pharmacy, or Medicine; specified qualifications include BSc, BA, PharmD, PhD, or MD.

Responsibilities

  • Act as the senior content expert on assigned accounts.
  • Lead content development, scientific reviewing, and mentorship of team members.
  • Develop and maintain expert knowledge of client products and therapy areas.
  • Interpret scientific data accurately and convey key communication points.
  • Ensure quality control and compliance with departmental procedures.
  • Manage project schedules and meet delivery deadlines.

Desired Qualifications

  • Training skills are desirable.

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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