Added
19 days ago
Type
Full time
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πŸ“‹ Description

  • Plan, direct, coordinate and deliver designated clinical study activities.
  • Serve as primary point-of-contact and escalation point to the client.
  • Coordinate and oversee external vendors to the timeline and budget.
  • Develop robust project plans, timelines, and risk management.
  • Collaborate with clinical operations and participate in activities as appropriate.
  • Prepare status updates and report progress to clients and senior management.

🎯 Requirements

  • Bachelor's degree in science/health; advanced degree preferred.
  • 7+ years clinical research; 4+ years direct PM experience.
  • Experience managing global, cross-functional trials.
  • Proficiency with ICH-GCP and SOPs; ability to implement.
  • Excellent communication and interpersonal skills.
  • Willingness to travel domestically and internationally.

🎁 Benefits

  • Discretionary annual bonus
  • Health insurance
  • Retirement savings benefits
  • Life insurance
  • Disability benefits
  • Parental leave
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