Join Our Team
Empowering Global Healthcare Through Expertise & Innovation
At Pharmaleaf, we partner with leading life sciences and pharmaceutical organizations worldwide. Our passionate team tackles complex regulatory, clinical, and safety challenges to advance global health. Explore open positions below and take the next step in your career.
Pharmacovigilance Specialist
Process expedited ICSR adverse event reports, perform drug safety signal detection, and manage global compliance reporting (FDA/EMA).
Maintaining 100% compliance with strict 15-day expedited reporting deadlines across multi-region clinical trials.
Clinical Research Associate (CRA)
Monitor investigative sites to verify patient safety, protocol compliance, data integrity, and GCP compliance for multi-center Phase II-IV trials.
Eliminating site monitoring backlogs while maintaining rigorous ICH-GCP protocol adherence.
Regulatory Affairs Manager
Lead global regulatory filings (IND, NDA, MAA), eCTD compilation, and act as primary liaison with FDA, EMA, and Health Canada.
Streamlining multi-jurisdictional dossier submissions to accelerate global drug approval timelines.
Senior Medical Writer
Author high-quality Clinical Study Reports (CSRs), protocols, investigator brochures, and safety narrative summaries for submission packages.
Transforming complex bio-statistical data into clear, regulatory-compliant documentation.
Biostatistician & Data Lead
Develop Statistical Analysis Plans (SAP), oversee CDISC SDTM/ADaM mapping, and perform SAS/R statistical programming for clinical trials.
Ensuring flawless CDISC data compliance and rapid statistical summary generation for regulatory reviews.
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General Inquiries
info@pharmaleaf.comCareer Inquiries
info@examplecareer.comPhone (US)
1 (415) 555-0199 6775