Global Clinical Operations Lead - Phase 2/3 Trials

Planet Pharma

Boston (MA)

On-site

USD 170,000 - 250,000

Full time

2 days ago
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Job summary

Planet Pharma in Boston is seeking an experienced Associate Director, Clinical Operations to lead a multinational Phase 2/3 trial. You will be the operational lead, partnering with cross-functional teams, investigators, and CROs to ensure study startup, execution, and closeout.

The role requires hands-on global study leadership with site activation, risk mitigation, and proactive management to ensure compliance with GCP and regulatory requirements while collaborating with Clinical Development,

Qualifications

  • Bachelor's degree in Life Sciences or related field.
  • Experience leading Phase 2 and/or Phase 3 clinical trials.
  • Proven track record managing global or regional clinical studies.
  • Biotech, pharma, or CRO industry experience.

Responsibilities

  • Lead clinical trial execution from startup through closeout.
  • Manage study timelines, milestones, and deliverables.
  • Drive site identification, activation, and enrollment strategies.
  • Oversee CRO and vendor performance for quality and timelines.
  • Collaborate with cross-functional teams (Clinical Development, Data Management, Biostatistics, Medical Monitoring, Regulatory).
  • Identify operational risks and develop mitigations.
  • Track progress and report to leadership.
  • Ensure compliance with GCP, SOPs, and regulations.

Skills

Clinical ops leadership
Project management
Global studies
Regulatory compliance

Education

Bachelor's degree in Life Sciences

Job description

Planet Pharma in Boston is seeking an experienced Associate Director, Clinical Operations to lead a multinational Phase 2/3 trial. You will be the operational lead, partnering with cross-functional teams, investigators, and CROs to ensure study startup, execution, and closeout.

The role requires hands-on global study leadership with site activation, risk mitigation, and proactive management to ensure compliance with GCP and regulatory requirements while collaborating with Clinical Development,

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