Senior Clinical Research Project Manager

Northwestern University

Chicago (IL)

In loco

USD 63.000 - 75.000

Tempo pieno

5 giorni fa
Candidati tra i primi

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Curriculum e lettera di presentazione personalizzati, pronti da inviare.

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Vantaggi offerti da questo lavoro

Health insurance
Tuition benefits for employee and/or/—
Paid vacation and holidays
Flexible work arrangements
Wellness programs
Generous retirement savings options

Descrizione del lavoro

Northwestern University seeks a senior research coordinator to manage highly complex biomedical and behavioral studies in obstetrics & gynecology. You will oversee multi-site projects, budgets, and regulatory compliance, coordinating with investigators and sponsors to meet milestones.

The role involves data management, grant preparation, and potential co-authorship of publications while ensuring adherence to all applicable laws and internal policies.

Competenze

  • Minimum 4-year bachelor’s degree in a social or health science or related field, or equivalent experience.
  • Master’s degree in a related field may substitute for experience and provide advanced qualifications.
  • Supervisory or project management experience is required.

Mansioni

  • Provide complex scientific and technical leadership for research projects.
  • Plan and implement protocols to support multiple studies and budgets.
  • Ensure compliance with GCP, IRB/ FDA CFR, and ICH guidelines.
  • Oversee day-to-day operations, resource planning and timelines.
  • Co-author scientific papers and assist with grant submissions.
  • Supervise staff and coordinate with PIs, nursing, and sponsors.

Conoscenze

Supervisory experience
Project management

Formazione

Bachelor's degree in social or health science or related
Master's degree in social or health science or related

Descrizione del lavoro

Northwestern University seeks a senior research coordinator to manage highly complex biomedical and behavioral studies in obstetrics & gynecology. You will oversee multi-site projects, budgets, and regulatory compliance, coordinating with investigators and sponsors to meet milestones.

The role involves data management, grant preparation, and potential co-authorship of publications while ensuring adherence to all applicable laws and internal policies.

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