Title: Clinical Trial Coordinator

Type of role: Contract to hire

Team: Global Clinical Operations

Work location: Home-based and virtual, travel as needed

Reports to: Senior Director, Clinical Development

About Comanche Biopharma

We are a preclinical biopharmaceutical company developing novel siRNA compounds for the treatment of preeclampsia. Our purpose is to lower the risks of pregnancy and prematurity worldwide by safely sustaining natural pregnancy and allowing for fetal maturation.

We envision a world where all pregnant women have access to safe and effective therapies that are evidence-based, cost-effective and sustainable. Our mission is to prevent or treat preeclampsia at its root cause.

Comanche Biopharma is named in honor and appreciation of the Numunuu people’s innovative utilization of the horse. Their recognition and adoption of the horse as a disruptive technology along with improvements made in quality, processes, and structures opened entirely new markets and reshaped nations. We believe the drug industry should be inspired by this example of purposeful innovation and take the opportunity to re-examine its approach to drug discovery, redesign its development processes for cost efficient high quality trials, radically change its distribution of new drugs, and redefine how value to society is measured. Comanche Biopharma is committed to the ethical representation of all people of color and economic status in our clinical development programs. We prioritize ensuring access to our drugs by those who need them most.

General description of the role

The Clinical Trial Coordinator (CTC) plays a key role in supporting the day-to-day execution of clinical trials, ensuring adherence to regulatory requirements and study protocols. Serving as a liaison with study sites, the CTC provides essential administrative and logistical support, including coordinating documentation, contracts and budget submissions in addition to overseeing trial operations. This role works closely with clinical leads to anticipate study needs, support site initiation, resolve operational challenges, and keep projects on track. The ideal CTC brings a proactive mindset, contributes innovative ideas, and streamlines team workflows and communication.

Responsibilities

• Support day- to – day operations of interventional clinical trials, ensuring timelines and deliverables are met
• Act as a site liaison, coordinating effectively between study sites, internal teams, and vendors,
• Assist with document management, including version control, filing, and maintaining study trackers using Google Workspace tools
• Troubleshoot and resolve site-level and operational issues proactively and efficiently
• Help with startup activities including site initiation, regulatory document collection, and logistics coordination
• Work closely with clinical leads to anticipate trial needs and implement organizational systems
• Participate in internal meetings and provide operational support to ensure the trial remains on schedule and compliant
• Bring forward innovative ideas and systems to improve team workflows and communication

Skills and capabilities

• Ability to travel to Boston 2-3 times a year for meetings
• Strong organizational skills
• Ability to manage multiple tasks and priorities simultaneously
• Confidence using Google Suite tools and navigating digital workspaces, especially for version control and collaboration
• Effective communicator
• Proactive and problem-solving mindset

Work qualifications

• 2+ years of women’s health experience
• 2+ years Interventional women’s health
• Preferred experience in labor and delivery, obstetrics, midwifery, fetal or neonatal medicines or similar fields

Education qualifications

• Bachelor’s degree preferred, but not required