Independently lead clinical projects within budget; may run international trials.
Primary client liaison for proposals and client presentations.
Liaise with project team and sponsors, including C-level stakeholders.
Lead all aspects of a clinical research trial(s).
Manage data management, safety, clinical, medical monitoring and biostatistics.
Prepare status updates with key deliverables and metrics.

🎯 Requirements

Degree in life sciences or related field, or equivalent.
5–7 years industry experience; 4+ years PM in CRO clinical trials.
Experience in Nephrology, Immunology or Autoimmune Disease.
GCP/ICH knowledge and clinical development process.
Willingness to travel domestically and internationally.
MS Office, MS Project, PowerPoint; CTMS, eTMF, EDC, IXRS; English.

🎁 Benefits

High-energy, collaborative team environment.
Opportunities to work on international trials.
Emphasis on work-life balance.

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