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Clinical Scientist - FSP

Parexel
Posted this week

LOCATION

United States · Remote

EXPERIENCE

Not specified

SALARY

Negotiable

SKILLS REQUIRED

Clinical Trial Protocol ComplianceMedical MonitoringStakeholder Management

Job description

Overview

Support the clinical and scientific conduct of clinical studies as a Clinical Scientist, working with the CS Protocol Lead and study team. The role may cover one or multiple studies and requires oncology experience.

What you'll do

  • Support clinical trial operational delivery across one or multiple studies.
  • Lead limited-scope studies when assigned.
  • Support adjudication activities and medical monitoring.
  • Prepare imaging data reconciliation and meeting materials.
  • Manage protocol deviations.
  • Liaise with cross-functional teams and study stakeholders.

What you'll need

  • Oncology experience.
  • Bachelor’s, master’s, or PhD in Life Sciences with 2+ years of relevant career experience.
  • More than 5 years of clinical development experience if you do not have a Life Sciences degree.
  • Advanced Excel skills, including pivot tables and VLOOKUPs.
  • MS Office experience, including Word, Excel, and PowerPoint.
  • Strong written and spoken English communication skills.
  • Willingness to travel for key company meetings.

Nice to have

  • Pharmaceutical experience.
  • Two years of medical monitoring experience.
  • Experience with adjudication support, imaging data reconciliation, meeting materials, and protocol deviation management.

Details

  • Remote in the United States.

Read the full description and apply on the company’s own careers page.

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Clinical Scientist - FSP