What You'll Do
Oversee interdisciplinary clinical studies in early development phases, ensuring adherence to Good Clinical Practice, regulatory standards, and internal procedures. Serve as the main point of contact between the organization and the client, managing expectations and delivering on contractual commitments across international sites.
Lead project teams to maintain quality, meet timelines, and control budgets. Monitor financial performance, track deliverables, and coordinate activities across multiple partners involved in study execution. Proactively identify risks, implement mitigation strategies, and ensure inspection readiness throughout the study lifecycle.
Develop project plans, lead internal and external meetings, and generate progress reports for stakeholders. Maintain accurate records in relevant systems and ensure completeness of trial master files. Contribute to bid defenses as a proposed project lead and support business growth through strong client engagement.
Requirements
- University degree in life sciences, medicine, pharmacy, nursing, or a related field
- Proven understanding of GCP, ICH guidelines, and applicable regulatory frameworks
- Strong organizational and time management abilities, with a focus on independent work
- Direct experience in therapeutic areas relevant to early-phase research
- Excellent written and verbal communication skills
- Proficiency in adopting new technologies
- Willingness and ability to travel up to 25% when needed
Preferred Qualifications
- Prior experience within a clinical research organization (CRO)
- Background in relevant therapeutic domains
Benefits
- Opportunities for career advancement and professional growth
- Access to technical and therapeutic training programs
- Supportive leadership and team environment
- Recognition from peers and colleagues
- Comprehensive rewards framework
- Inclusive workplace culture that values authenticity
- Collaboration with global experts shaping healthcare innovation
