Senior Medical Operations Lead - Remote

Parexel

Montpelier (VT)

Remote

USD 120.000 - 160.000

Vollzeit

Vor 3 Tagen
Sei unter den ersten Bewerbenden

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

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Zusammenfassung

Parexel in the United States is seeking a Senior Clinical Scientist to lead or support complex studies, ensuring clinical and scientific execution of the protocol. The SCS may serve as the lead clinical contact for internal and external stakeholders and will contribute to trial design, endpoint development and trial governance.

The role emphasizes leadership in Medical Monitoring, data review, and collaboration with clinical teams.

Qualifikationen

  • Experience reviewing and resolving study related data issues.
  • Demonstrated oral and written communication skills.
  • Proficiency in Microsoft Office (Outlook, Word, Excel, PowerPoint); OneNote preferred.
  • Ability to motivate teams, delegate, take feedback and adapt.

Aufgaben

  • Lead or support clinical studies, accountable for execution.
  • Serve as clinical lead and primary contact for stakeholders.
  • Lead Medical Monitoring team and develop the Medical Monitoring Plan.
  • Review safety data and SAE reports; address data issues.
  • Collaborate on trial design, endpoint development, and governance.
  • Prepare scientific materials and present at Investigator Meetings.
  • Coordinate planning of lab, bio specimens and imaging specs.
  • Contribute to CSRs, CTDs/WMAs with medical writing.
  • Mentor other Clinical Scientists and ensure regulatory compliance.
  • Support Parexel standards and training requirements.

Kenntnisse

Data issue resolution
Oral & written communication
MS Office proficiency
Team leadership

Ausbildung

BS/BA Life Sciences
MS/PhD Life Sciences

Tools

OneNote

Jobbeschreibung

Parexel in the United States is seeking a Senior Clinical Scientist to lead or support complex studies, ensuring clinical and scientific execution of the protocol. The SCS may serve as the lead clinical contact for internal and external stakeholders and will contribute to trial design, endpoint development and trial governance.

The role emphasizes leadership in Medical Monitoring, data review, and collaboration with clinical teams.

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