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Parexel

End-to-end clinical trials and regulatory consulting

Clinical Scientist - Functional Service Provider

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeRemote in USANo salary listed

About the Job

Requirements

  • Demonstrated oral and written communication skills.
  • Experience with Microsoft Office Suite, including Word, Excel, and PowerPoint.
  • Advanced Excel skills, including pivot tables and VLOOKUPs.
  • Proficiency in written and spoken English.
  • Willingness to travel as required for key company meetings.
  • Oncology experience is required.
  • Experience with adjudication support, medical monitoring, imaging data reconciliation, preparation of meeting materials, and protocol deviation management.
  • A Bachelor's, Master's, or PhD in Life Sciences and at least 2 years of relevant career experience; alternatively, a Bachelor's degree and significant clinical development experience exceeding 5 years if the candidate does not have a Life Sciences degree.

Responsibilities

  • Assist the Clinical Scientist Protocol Lead and study team with the clinical and scientific conduct of clinical studies, including adjudication support, medical monitoring, imaging data reconciliation, preparation of meeting materials, and protocol deviation management.
  • Support one or multiple studies and potentially lead a study with limited scope, such as survival follow-up.
  • Liaise with cross-functional teams as appropriate.
  • Interact with internal and external stakeholders, including study sites and committees, to support clinical study objectives.
  • Complete required training, timesheets, expense reports, and CV updates.
  • Maintain working knowledge of and comply with Parexel processes, ICH-GCPs, and other applicable requirements.

Desired Qualifications

  • Pharmaceutical experience is beneficial but not required.
  • Two years of medical monitoring experience 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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