As a Sponsor-side CTM in a fast-growing start-up, you will have broad responsibility across study start-up, execution, vendor oversight, compliance, and budget management. This is a key role for someone who thrives in a lean environment, takes ownership, and enjoys building structure while delivering high-quality clinical trials.
Key Responsibilities:
– Own end‑to‑end study execution from start‑up to close‑out
– Manage sites, CROs, and specialist vendors
– Ensure compliance with ICH‑GCP and inspection readiness
– Drive timelines, quality, and budgets
– Act as the operational link across internal teams and external partners
Qualifications & Experience:
– Bachelor’s or Master’s degree in Life Sciences, Biomedical Sciences, or a related field.
– Several years of experience in Clinical Operations, preferably with Sponsor-side oversight responsibilities.
– Solid understanding of clinical trial conduct, ICH‑GCP, and regulatory requirements.
– Hands-on experience managing CROs, vendors, sites, and study budgets.
– Experience working in small, growing, or resource-constrained organizations is a strong plus.
Key Competencies:
– Strong ownership mentality and ability to work independently.
– Excellent organizational and project management skills.
– Pragmatic, solution-oriented, and comfortable with ambiguity.
– Strong communication and stakeholder management skills.
– Detail-oriented with a strong focus on quality, compliance, and delivery.
– Able to balance speed, cost, and quality in a start-up setting.