Cambrian Bio

www.cambrianbio.com

1 Job

27 Employees

About the Company

Cambrian Bio is a clinical-stage drug development company building the medicines that will modernize healthcare in the 21st century. Our focus lies in creating innovative therapeutics designed to treat and ultimately prevent some of today's most debilitating chronic diseases, including platforms targeting the critical metabolic pathways that decline with age such as AMPK activation, mitochondrial function, and mTORC1 inhibition, to extend the period of life spent in good health.

Listed Jobs

Company Name: Cambrian Bio
Job Title: Clinical Trial Associate
Job Description: Job Title: Clinical Trial Associate Role Summary: Provide day‑to‑day operational and administrative support for clinical trial planning, execution, and close‑out across the entire study lifecycle. Work collaboratively with Clinical Operations, CROs, finance, legal, and other cross‑functional teams to ensure timely and compliant trial conduct. Expectations: - Execute trial support tasks with high attention to detail and follow‑through. - Manage multiple concurrent priorities in a dynamic early‑stage biotech environment. - Maintain accurate and organized trial documentation, trackers, and timelines. - Escalate issues promptly and support seamless communication among stakeholders. Key Responsibilities: - Assist with study startup through close‑out activities, including the preparation, organization, and maintenance of essential documentation (TMF/ISF, tracking files). - Coordinate contract and document flow with CROs, vendors, finance, legal, and business operations. - Track contract status, vendor deliverables, and trial milestones; support escalation of issues. - Maintain study trackers, plans, and internal status updates. - Support invoice tracking and reconciliation with finance. - Provide general operational and administrative assistance to ensure efficient trial execution. Required Skills: - Strong organizational and time‑management abilities. - Detail‑oriented, with a proven track record of accurate document handling. - Ability to support multiple concurrent work streams. - Excellent written and verbal communication skills. - Familiarity with GCP‑regulated environments and clinical trial documentation systems. - Proficient in Microsoft Office (Excel, Word, PowerPoint); experience with electronic trial master file (eTMF) systems is a plus. Required Education & Certifications: - Bachelor’s degree in life sciences, health sciences, or a related field. - Minimum 2 + years of experience in clinical operations, clinical trial support, or a related role within biotech, pharma, or a CRO. - Prior experience in an early‑stage biotech company is required. - Understanding of GCP and regulatory documentation standards.