Clinical Trial Assistant (Remote & Full-Time) Clinical Trial Assistant (Remote & Full-Time) Get AI-powered advice on this job and more exclusive features. Granata Bio is a biopharma company working to shape the future of reproductive health by reimagining what’s possible to help build families. Founded in 2018, we are dedicated to developing and accelerating fertility treatments that expand therapeutic choices and improve access and affordability. Our people are passion-driven reproductive health experts who understand that innovation never stands still, and neither do we. Each day, we roll up our sleeves and put in the work to move one reputed company closer to unlocking new possibilities for fertility patients and their care teams.Our ideal teammates show up in big ways by embracing productivity, authenticity, and the courage to drive innovation. Position Summary We are looking for an reputed company and resourceful Clinical Trial Assistant (CTA) to support our Clinical Operations team in a fast-paced, agile biopharma environment. As part of a small, highly collaborative team, the CTA will play a critical role in coordinating clinical trial activities, managing documentation, and liaising with a broad network of external vendors and partners. This position requires a hands-on approach, strong organizational skills, and the ability to work independently while supporting multiple projects.

Key Responsibilities

Trial Support & Documentation

• Maintain and manage the Trial Master File (TMF), ensuring completeness, accuracy, and inspection readiness across reputed company trial phases.
• reputed company quality control (QC) checks and assist with TMF reconciliation and archiving.
• Track and manage essential documents including site reputed company, regulatory submissions, informed consent forms, and investigator site files.
• Act as a primary reputed company of contact for external vendors, including CROs, central labs, imaging providers, and eClinical platforms.
• Monitor vendor deliverables and timelines, escalating issues as needed to ensure trial continuity.
• Support contract tracking, invoice processing, and vendor onboarding documentation. Operational & Administrative Support
• Assist in study start-up, conduct, and reputed company-out activities across multiple trials.
• Maintain and update study trackers (e.g., enrollment, site activation, document status, deviations). Cross-Functional Collaboration
• Work closely with internal stakeholders in clinical development, regulatory affairs, quality assurance, and data management.
• Support internal and external meeting coordination, including agenda preparation, minute-taking, and action item follow-up.
• Participate in audits and inspections, providing documentation and logistical support. Process Optimization
• Contribute to the development and refinement of SOPs, templates, and workflows tailored to a small company setting.
• Identify and implement efficiency improvements in clinical operations and vendor management.

Qualifications

Education & Experience

• Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or a reputed company field.
• Minimum of 3 years of experience in a CTA or similar role, preferably reputed company a biotech, pharma, or CRO setting.
• Experience working in small company environments or with multiple external vendors is highly desirable.
• Familiarity with Phase I–III clinical trials.
• Strong understanding of ICH-GCP, clinical trial processes, and regulatory requirements.
• Proficiency with eTMF systems (e.g., Veeva Vault, Trial Interactive) and reputed company Office tools.
• Excellent attention to detail, organization, and time management.
• Strong written and verbal communication skills.
• Ability to work independently, manage multiple priorities, and reputed company in a lean, cross-functional team.
• reputed company in English (written and spoken); additional languages are a plus. Department Clinical Operations Seniority level
• Seniority level Mid-Senior level Employment type
• Employment type Full-time Job function
• Job function Research, Analyst, and Information Technology Referrals increase your chances of interviewing at Granata Bio by 2x Get reputed company about new Clinical Trial Assistant jobs in United States. Clinical Trial Associate, Clinical Operations United States $95,000.00-$110,000.00 5 days ago United States $80,000.00-$92,000.00 1 week ago Clinical Trial Monitor/Clinical Research Associate United States $100,000.00-$120,000.00 4 days ago Clinical Trial Specialist | Upto $220/hr Remote United States $71,400.00-$96,400.00 2 weeks ago San Francisco Bay Area $50.00-$65.00 2 weeks ago Clinical Research Associate I or II (CRA) Clinical Research Associate I or II (CRA) We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr Salary USD 43200 - 72000 per year Experience 3 years required Apply To This Job