Senior Clinical Project Leader - Cardiovascular (Remote)

Actalent

United States

Remote

USD 110,000 - 124,000

Full time

4 days ago
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Benefits offered by this job

Medical, dental & vision
401(k) plan
Life Insurance
Paid time off

Job summary

Actalent is seeking an experienced Clinical Project Leader III for a fully remote, homebased role supporting large Phase II–IV cardiovascular and metabolic trials from startup to closeout. You will serve as the operational lead, coordinating sponsors, sites, investigators, vendors, and internal teams to keep trials on time and in compliance.

Qualifications include 7+ years in clinical project leadership, a related bachelor's degree, and deep knowledge of GCP/FDA regulations, with proven global

Qualifications

  • 7+ years in clinical project leadership, preferably Phase II–IV.
  • Bachelor's degree in a relevant field or equivalent experience.
  • Strong understanding of GCP and FDA regulations.
  • Experience leading global, multi-country cardiovascular/metabolic trials.
  • Excellent cross-functional collaboration and communication skills.

Responsibilities

  • Lead day-to-day operations of Phase II–IV trials from startup through closeout.
  • Ensure studies stay on schedule, within scope, and compliant with protocol, GCP, and regulatory requirements.
  • Coordinate activities between sponsors, sites, investigators, vendors, and internal teams.
  • Identify operational risks, troubleshoot issues, and implement practical solutions to keep projects on track.
  • Oversee site startup, regulatory submissions, essential documents, and site readiness.
  • Provide guidance and mentorship to junior team members.

Job description

Actalent is seeking an experienced Clinical Project Leader III for a fully remote, homebased role supporting large Phase II–IV cardiovascular and metabolic trials from startup to closeout. You will serve as the operational lead, coordinating sponsors, sites, investigators, vendors, and internal teams to keep trials on time and in compliance.

Qualifications include 7+ years in clinical project leadership, a related bachelor's degree, and deep knowledge of GCP/FDA regulations, with proven global

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