Us Study Start Up Lead

Pharmajobber

Base: $115,500 to $192,500; bonus/equity: annual b...
Fully remote
Clinical trial start-up management
Study start-up metrics accountability
Cross-functional team coordination
The Study Start Up Lead is responsible for providing leadership in the execution of operational strategy and management of start-up activities for all clinical trials, across all therapy areas

Job Summary

  • The Study Start Up Lead is responsible for providing leadership in the execution of operational strategy and management of start-up activities for all clinical trials, across all therapy areas.
  • This position offers an annual bonus and eligibility to participate in a share based long term incentive program dependent on the role level, along with comprehensive health care, retirement, paid holidays, vacation, and caregiver/parental leave benefits.
  • GSK is a global biopharma company focused on innovation in specialty medicines and vaccines, committed to creating an environment where people can thrive and focusing on ambitious patient outcomes and accountability.

Matching Summary

The Study Start Up Lead is responsible for providing leadership in the execution of operational strategy and management of start-up activities for all clinical trials, across all therapy areas.

Salary

Base: $115,500 to $192,500; Bonus/Equity: annual bonus and share based long term incentive program; Benefits: health care, retirement, paid holidays, vacation, caregiver/parental leave

Skills & Requirements

Must-have

  • clinical trial start-up management
  • study start-up metrics accountability
  • cross-functional team coordination
  • clinical operations leadership
  • regulatory compliance management
  • project management skills
  • vendor and recruitment strategy management

Nice-to-have

  • oncology study start-up experience
  • clinical trial diversity planning
  • advanced MS Office skills
  • strong communication skills
  • process improvement participation
  • experience with FSP CRO model

Key Requirements

  • Bachelor’s degree in General Science or related field
  • 5+ years clinical operations experience or 10+ years study management experience
  • project management skills
  • experience with clinical trial regulations
  • English and local language proficiency

Work Rights

Not specified

Tailored Resume

Cover Letter