Clinical Trial Associate

Company DescriptionFounded in 2025, Amandala Neuro is a rapidly-growing biotech startup spun out ahead of the strategic combination of Beckley Psytech and Atai Life Sciences (now AtaiBeckley) to enable focused development of ELE-101 (an IV dosage form of psilocin, the active metabolite of psilocybin), with a pipeline of follow-up candidates to address poorly-controlled neuropsychiatric conditions.We are dedicated to helping patients suffering from neurological and psychiatric disorders by developing a pipeline of short-acting psychedelic compounds. Our vision is for clinically validated psychedelic medicines to be integrated into medical practice in order to help patients in need around the world suffering with these profoundly debilitating conditions.Role DescriptionWe are seeking a detail-oriented Clinical Trial Associate with a minimum of one year of clinical research experience to support sponsor oversight of Phase 1 and 2 programs. This role will play a critical part in maintaining Trial Master File quality, ensuring documentation integrity, and coordinating communications across CROs and internal stakeholders in a growing, biotech environment. The role reports to the Director of Clinical Operations.Key ResponsibilitiesSupport sponsor oversight of Phase 1 and 2 clinical trials conducted through CRO partnersOversight of CRO managed eTMFs, to ensure maintenance, contemporaneous and complete Trial Master File (eTMF)Perform reviews of the TMF for quality, accuracy, and regulatory complianceCoordinate document flow between CROs, sites, vendors, and internal teamsMaintain tracking logs (regulatory, safety, enrollment, milestones)Support preparation for regulatory inspections and auditsAssist in study start-up activities, including essential document collectionDocument meeting minutes and maintain action item trackersSupport controlled document management and version control processesQualificationsExperience with managing and maintaining Informed Consent and Trial Master File (TMF) documentationKnowledge of clinical trial processes, including Clinical Trials and Clinical OperationsResearch skills, including the ability to analyze, interpret, and summarize dataStrong attention to detail and organizational skillsAbility to collaborate effectively in a remote team environmentFamiliarity with regulatory requirements and Good Clinical Practice (GCP) guidelines including ICH-GCP R3Bachelor’s degree in life sciences, healthcare, or a related fieldMinimum 1 year experience in a clinical research roleRequirements added by the job posterBachelor's Degree

Created: 2026-05-02