Remote Medical/Clinical Scientist – Bladder Late-Phase

Syneos Health/ inVentiv Health Commercial LLC

Wisconsin

A distancia

USD 68.000 - 140.000

Jornada completa

Hace 8 días

Una candidatura completa en un minuto

Currículum y carta de presentación personalizados, listos para enviar.

Supera los filtros ATS

Ventajas ofrecidas por este puesto de trabajo

Company car or car allowance
Health benefits (Medical, Dental and V
Company match 401k
Employee Stock Purchase Plan
Bonuses/commissions based on company/
Paid time off (PTO) and sick time

Descripción de la vacante

Syneos Health seeks a Medical/Clinical Scientist - ONC - Bladder Late Phase (sponsor-dedicated/Remote) to support medical plans and data reviews. You will collaborate with Medical Directors and external experts to gather medical input and ensure data readiness for decision-making.

Responsibilities include regular ad-hoc data reviews, preparing medical review summaries, and coordinating safety and data integrity across study teams while complying with ICH and GCP standards.

Formación

  • Experience in medical data review and data visualization.
  • Ability to identify risks from data patterns.
  • Familiarity with data privacy guidelines, ICH and GCP.

Responsabilidades

  • Develop medical plans with Medical Director and coordinate input from experts.
  • Perform regular and ad-hoc medical data reviews and analyze data for risks.
  • Authors medical data queries and reviews query responses; assist in patient profiles review.
  • Collaborate with Medical Directors for data review and safety meetings; lead meetings as appropriate.
  • Manage project scope, milestones and liaise with customers and vendors on data review.
  • Adhere to ICH, GCPs and data privacy guidelines; support audits as needed.

Descripción del empleo

Syneos Health seeks a Medical/Clinical Scientist - ONC - Bladder Late Phase (sponsor-dedicated/Remote) to support medical plans and data reviews. You will collaborate with Medical Directors and external experts to gather medical input and ensure data readiness for decision-making.

Responsibilities include regular ad-hoc data reviews, preparing medical review summaries, and coordinating safety and data integrity across study teams while complying with ICH and GCP standards.

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