Remote Oncology Clinical Study Physician

Parexel

Salem (OR)

Remote

USD 180.000 - 230.000

Vollzeit

14 Tage+

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Zusammenfassung

Parexel is seeking a Clinical Study Physician to join our globally deployed clinical development team. This fully remote role focuses on medical oversight for oncology trials, with emphasis on protocol input, data integrity, and regulatory interactions.

The SP will lead medical content development, risk-based quality strategies, and cross-functional collaboration across trials and site teams, ensuring high medical quality from kickoff through reporting.

Qualifikationen

  • MD with medical license and clinical experience
  • Minimum 4 years of active clinical experience; internal medicine/general practice preferred
  • Experience in pharma/CRO medical functions is desirable

Aufgaben

  • Provide medical oversight across trial design, startup, conduct and reporting
  • Develop and critique trial protocols, CQMP, and data management inputs
  • Lead medical content for patient information and informed consent
  • Respond to medical queries from investigators and sponsor teams
  • Participate in regulator/ethics communications
  • Collaborate with cross-functional teams and external experts
  • Support endpoint adjudication and monitoring boards as applicable
  • Maintain Parexel standards and training compliance

Kenntnisse

Interpersonal skills
Analytical thinking
Presentation skills
Training skills
Teamwork in international environment
Proactivity
Digital literacy
Excellent communication

Ausbildung

MD, licensed physician
Internal medicine or general practice specialization

Tools

MS Office
eCRF systems experience

Jobbeschreibung

Parexel is seeking a Clinical Study Physician to join our globally deployed clinical development team. This fully remote role focuses on medical oversight for oncology trials, with emphasis on protocol input, data integrity, and regulatory interactions.

The SP will lead medical content development, risk-based quality strategies, and cross-functional collaboration across trials and site teams, ensuring high medical quality from kickoff through reporting.

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