Principal Investigator - #2142761

Overview

We are seeking a qualified and experienced Principal Investigator (PI) to join our clinical research team. The ideal candidate will be a licensed physician with commercial clinical trial experience across multiple therapeutic indications and seeking or holding an Approbatin license. This is a key leadership role in the conduct of clinical trials at our clinet's site, ensuring participant safety and data integrity.

Key Responsibilities

• Serve as the Principal Investigator for industry-sponsored clinical trials across various therapeutic areas
• Oversee the clinical and operational conduct of studies in compliance with the protocol, GCP, ICH guidelines, and all applicable regulatory requirements.
• Supervise and medically evaluate study participants, assess adverse events, and provide clinical oversight of the study team.
• Collaborate with sponsors, CROs, and internal staff to support site feasibility, study start-up, patient recruitment, and successful execution of clinical trials.
• Ensure proper documentation of source data, electronic case report forms (eCRFs), and all essential trial documents.
• Maintain accurate and up-to-date training and licensing records, including qualifications required for an Approbation license.
• Participate in monitoring visits, audits, and inspections as needed.
  
  

Qualifications

• Medical degree (MD or equivalent) with active, unrestricted medical license.
• Eligible for or currently holding an Approbation license
• Minimum of 2 years of experience as a PI or Sub-Investigator in commercial (industry-sponsored) clinical trials.
• Demonstrated experience working across multiple therapeutic indications.
• Has experiencebudget manamgement for the site and can think creatively to boost revenue for the site.
• Strong knowledge of ICH-GCP and local/international regulatory requirements.
• Excellent leadership, communication, and organizational skills.
  
  

Preferred Skills

• Experience with site initiation, patient recruitment strategies, and clinical operations.
• Familiarity with electronic data capture (EDC) systems and regulatory document platforms.
• Bilingual or multilingual abilities are a plus, especially in [insert relevant languages].
  
  

We Offer

• Competitive compensation
• Supportive research team and infrastructure
• Opportunities for professional development and training
• Involvement in cutting-edge clinical research with top sponsors