Location
Remote (APAC)
Seniority
Senior · 7+ years exp
Employment
Full-Time
Confirmed on the employer's own hiring board on Nov 9, 2026. First seen by Alion on Nov 4, 2026. Planet Pharma scores B on the Alion truth index.
Overview
Company
Impact
Profile match
Planet Pharma is a life sciences recruitment and staffing firm headquartered in Deerfield, Illinois, that places contract and permanent professionals with pharmaceutical, biotechnology, medical device and contract research organizations. Founded in 2012, it offers contract and direct hire staffing, strategic resourcing, executive search, functional service provider models and global workforce solutions, with offices in Deerfield, Chicago and Raleigh and placements in the United States, Europe and Asia. Planet Pharma recruits for clients research scientists and associates, clinical trial managers, quality engineers, compliance specialists, medical writers and production supervisors.
Senior Project Manager - Clinical Research
About the Opportunity
Our client is a highly respected global clinical research organisation delivering innovative clinical trial solutions across a broad range of therapeutic areas. With a strong international presence and a reputation for scientific excellence, they partner with biotechnology and pharmaceutical companies to advance life-changing treatments worldwide.
They are seeking an experienced Senior Project Manager to lead the delivery of regional and global clinical trials. This is a client-facing role requiring strong project leadership, operational oversight, budget management, and stakeholder engagement.
Key Responsibilities
- Lead the end-to-end delivery of Phase II-IV clinical trials from start-up through close-out.
- Manage cross-functional project teams, vendors, and study stakeholders.
- Act as the primary point of contact for sponsors and ensure high levels of client satisfaction.
- Oversee study timelines, budgets, forecasts, and resource planning.
- Drive study start-up activities including feasibility, site selection, regulatory submissions, and site activation.
- Monitor project progress, identify risks, and implement mitigation plans.
- Ensure studies are conducted in compliance with ICH-GCP, applicable regulations, and company SOPs.
- Support business development activities, including scope changes and bid defence meetings where required.
- Mentor and develop junior project management and clinical operations staff.
About You
- Bachelor’s degree in Life Sciences or a related field.
- 7+ years of clinical research experience, including 4+ years in project management.
- Strong experience managing Phase II and/or Phase III clinical trials.
- Experience within a CRO, pharmaceutical, or biotechnology environment.
- Demonstrated client-facing and stakeholder management experience.
- Strong understanding of ICH-GCP, regulatory requirements, and clinical trial operations.
- Proven experience managing study budgets and financial performance.
- Oncology and/or Renal clinical trial experience highly regarded.
- Mandarin language skills are advantageous.
What’s on Offer
- Opportunity to work with a leading global clinical research organisation.
- Exposure to complex international clinical trials.
- Flexible hybrid or remote working arrangements.
- Strong career development and progression opportunities.
- Collaborative and supportive global team environment.
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