We are looking to hire a candidate with the skills sets mentioned and experience for one of our clients within the pharmaceutical Industry. This is a Remote position.
Job Summary
We are seeking an experienced Project Manager with a background in
clinical trials, CRO operations, and pharmaceutical programs
. The ideal candidate will manage cross-functional teams, support product-related initiatives, and ensure successful execution of clinical and operational project activities.
Key Responsibilities:
Lead and manage clinical trial and pharmaceutical projects from planning through delivery.
Coordinate cross-functional teams including Clinical Operations, Data Management, Regulatory, and Product teams.
Develop project plans, timelines, budgets, and risk mitigation strategies.
Oversee vendor/CRO activities, ensuring compliance with timelines, quality standards, and regulatory requirements.
Track study progress, identify issues, and communicate project updates to stakeholders.
Support product development efforts and collaborate with product managers on requirements, enhancements, and launches.
Maintain study documentation and ensure adherence to GCP, ICH, and company SOPs.
Monitor KPIs, milestones, and deliverables to ensure projects stay on schedule and within scope.
Qualifications:
3-7 years of
project management
experience in
clinical trials, CRO, or pharma
.
Strong understanding of GCP, ICH, and regulatory requirements.
Experience working with clinical systems, study teams and external vendors.
Product management or product support experience is a plus.
Excellent communication, organization, and stakeholder management skills.
Ability to manage multiple projects in a fast-paced environment.
Other details :
Location:
Remote
Duration:
6 months - 1 year (High possibility of extension)
Pay Rate:
$62 on W2 and $70 on C2C
Documentation Required:
ID proof
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