{"id":705648,"url":"https://alion.io/job/agomab-senior-clinical-trial-associate","title":"Senior Clinical Trial Associate","company":{"id":670680,"name":"Agomab Therapeutics","domain":"agomab.com","url":"https://alion.io/company/agomab","size_band":"51-200","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Pinpoint","truth_index":null},"role":"Biotech","role_family":"Biotech","seniority":"senior","employment_type":"full_time","work_mode":"hybrid","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"explicit","locations":["Antwerp, Belgium"],"countries":["BE"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":68000,"max_usd":141000,"period":"year","method":"global_role_cell_scaled_by_country","sample_n":543},"experience_years_min":5,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"Good Clinical Practice","optional":false},{"name":"Microsoft Office","optional":false},{"name":"SharePoint","optional":false}],"status":"live","first_seen_at":"2026-09-10T03:51:41Z","employer_posted_date":"2026-10-20","last_verified_at":"2026-11-04T14:00:22Z","board_verified":true,"closed_at":null,"days_open":55,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":55},"description":"The Senior Clinical Trial Associate (CTA) is providing high-quality administrative and operational support to the Clinical Operations Team. In this role, you will report to the Head of Clinical Operations. You will play a critical part in ensuring the efficient, compliant, and timely execution of our clinical trials. The CTA is responsible for maintaining study documentation, supporting trial logistics, and ensuring inspection readiness while working closely with Clinical Trial Managers (CTMs), vendors, and study teams. The role requires strong organizational skills, attention to detail, and the ability to manage multiple priorities in a fast-paced biotech environment.\n\nAll activities are conducted in compliance with ICH-GCP, company SOPs, and applicable regulatory requirements.\nKey Responsibilities\nThe key accountabilities and responsibilities of the Senior Clinical Trial Associate include:\nAssist the CTM in the preparation, distribution and maintenance of study related documents;\nManage the Trial Master File (TMF) to ensure completeness, accuracy and compliance with internal procedures and regulatory standards, in collaboration with the CTM;\nEnsure inspection readiness of the TMF at all times and archiving of the TMF at study completion;\nFacilitate communication with trial sites, vendors and internal team members;\nMaintain study trackers, reports and documentation systems and distribute information to stakeholders in collaboration with the CTM;\nCoordinate and schedule meetings, teleconferences, and logistics for the clinical study teams;\nManage the request of clinical trial insurances with the insurance broker and reports on the activity to the CTM;\nSupport study-specific clinical sample tracking and logistics;\nAssist with vendor coordination and follow-up activities;\nAssist in the organization of meetings, trainings and other clinical operations events;\nAdhere to company policies, SOPs and guidelines;\nSupport quality control of documentation and operational processes and contribute to continuous improvement of clinical operations workflows.\nSkills, Knowledge and Expertise\n Who are you?\n\nBachelor’s degree in an administrative, scientific, or business-related field, or equivalent experience.\n5+ years of experience supporting clinical trial operations in biotech, pharma, or CRO environments.\nWorking knowledge of ICH-GCP and clinical trial documentation requirements.\nExperience in coordination, tracking, and document management.\nProficiency in Microsoft Office (Word, Excel, PowerPoint, SharePoint) and general digital tools.\nExcellent written and verbal communication skills in English.\nHigh attention to detail and strong follow-up skills.\nAbility to manage multiple priorities in a dynamic environment.\nHighly organized and self-driven, strong time management and prioritization skills, and collaborative team player with a proactive problem-solving mindset\nBenefits\nBenefits\n\nThe opportunity to develop pioneering science in a young biotech company;\nChallenging and innovative work environment as part of a driven team;\n Flexibility and ownership, based in Antwerp, Belgium, with remote working options tailored to individual needs;\nCompetitive salary and benefits;\nAn agile and fast paced 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