Associate Director - Research (kimmel Cancer Center)

Jefferson Health

Philadelphia, PA, United States
Gcp/ich compliance
Clinical trial operations
Regulatory documentation
Incumbent will be responsible for ensuring that clinical trials in the Clinical Trials Office (CTO) are conducted in accordance with Federal, and State governance, institutional regulations, GCP/ICH, and follow all applicable policy

Job Summary

  • Incumbent will be responsible for ensuring that clinical trials in the Clinical Trials Office (CTO) are conducted in accordance with Federal, and State governance, institutional regulations, GCP/ICH, and follow all applicable policy.
  • The Associate Director will be responsible for all non-clinical personnel of the office but work closely with Nurse Manager of the Outpatient Infusion Center.
  • Jefferson offers a comprehensive package of benefits for full-time and part-time colleagues, including medical (including prescription), supplemental insurance, dental, vision, life and AD&D insurance, short- and long-term disability, flexible spending accounts, retirement plans, tuition assistance, as well as voluntary benefits.

Matching Summary

Incumbent will be responsible for ensuring that clinical trials in the Clinical Trials Office (CTO) are conducted in accordance with Federal, and State governance, institutional regulations, GCP/ICH, and follow all applicable policy.

Skills & Requirements

Must-have

  • GCP/ICH compliance
  • clinical trial operations
  • regulatory documentation
  • data integrity and management
  • clinical trial billing compliance

Nice-to-have

  • interacts with co-workers
  • values of Jefferson
  • functional disease specific research units

Key Requirements

  • Bachelor’s degree required
  • Master’s degree preferred
  • RN required
  • Human subjects training
  • 8 years of experience in clinical trials management
  • 5 years of experience managing/supervising direct reports
  • Knowledge of oncology cooperative groups’ regulatory process
  • Knowledge of Code of Federal Regulations
  • Knowledge of good clinical practices (GCPs)
  • Knowledge of ICH Guidelines
  • Experience with grant writing
  • Experience with report writing
  • Excellent computer database skills
  • Excellent scientific/medical writing skills
  • Excellent project management skills
  • Excellent oral and written communication skills

Work Rights

Not specified

Tailored Resume

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