Senior Clinical Trial Assistant

JOB TITLE : (Sr.) Clinical Trial Assistant, Clinical Operations

LOCATION : Seaport, Boston, MA (Hybrid) DATE PREPARED : August 14, 2025

JOB SUMMARY :

Aveo Oncology is looking for an experienced Clinical Operations professional. The Clinical Trial Assistant will report to the Vice President or Associate Director, Clinical Operations. The role is primarily responsible for supporting close interactive oversight to ensure exceptional execution of AVEO Oncology clinical studies. The Clinical Trial Associate will also be accountable for participating in departmental efficiency initiatives in support of department excellence.

The Clinical Trial Assistant will support monitoring clinical studies across geographic regions, in adherence to Good Clinical Practices (GCPs), appropriate Standard Operating Procedures (SOPs), regulatory authority guidance and directives such as Food and Drug Administration (FDA), and International Conference on Harmonization (ICH) guidelines.

The Clinical Trial Assistant will support ensuring quality data for all clinical trials. The Clinical Trial Assistant will support the interactions with CROs and other 3rd party vendors to ensure study milestones and deliverables are achieved according to agreed quality standards and timelines so that data is suitable for regulatory submissions and publications. The Clinical Trial Assistant will also support metrics-based assessments to measure departmental and 3

rd

party performance on a quarterly basis to meet corporate goals. The Clinical Trial Assistant will also assist with troubleshooting routine site inquiries.

Outside interfaces may include other Aveo Oncology business groups and subsidiaries in the US and abroad, governmental, academic, community and industry organizations.

The Clinical Trial Assistant will not have assigned direct reports.

Good written and verbal communication skills and attention to detail are required and are equally important. The ideal candidate for this role is an individual who is excited to take on new challenges in a dynamic environment. To be successful, the candidate is committed to collaboration and a data driven approach to align with the team's brand and culture.

PRINCIPAL DUTIES :

Study Management and Leadership

Collaborate closely with Clinical Team in support of study execution

Support planning and logistics for internal and external meetings and preparation of agendas, meetings, and meeting minutes

Support oversight of site compliance with study protocol

Support and maintain metrics-based tools to assess departmental and 3

rd

party performance on a quarterly basis to meet corporate goals

Support adherence to internal procedures for study planning, study conduct, close out and reporting

Support all inspection readiness and quality initiatives for assigned studies

Maintains and reviews various study-related tracking systems to determine and report status of clinical trial documents (i.e., distribution, status, retrieval of such documents as protocol, IB, etc.)

Support Clinical Project Manager and Clinical Research Associate for meeting minutes as requested

Support study team in tasks such as presentations, mailings to sites, assembly and distribution of Investigator Site Files, newsletters and handling of study documents, copying and filing, correspondence. The CTA will maintain site contact lists, trackers, etc.

Support the Clinical Project Manager for review of invoices.

Generate mass mailings upon request of the Clinical Project Manager.

Perform administrative tasks to support team members with clinical trial execution as needed.

CRO, 3rd Party Vendor Management and Oversight for assigned studies

Support tracking of operational study timelines and monitor operational performance metrics through the life of the study, support issue resolution

Support Biosample tracking from sites to central lab sample management to central analytical lab.

Assist in the creation and review of informed consents, case report forms, study operations manuals, monitoring tools, and other study-related materials

Support site level progress ensuring timely data collection, source document verification, and query resolution

Develop and maintain audit-ready clinical trial documentation in the TMF : Manage and track regulatory / IRB / EC documentation, IND Safety Letter distribution, Confidentiality Disclosure Agreements, and other clinical trial documents

Contact clinical sites and / or CROs to complete study files and regulatory document collections to ensure TMF documents are filed in TMF in a timely manner

Ensure timely safety reporting at assigned investigative sites

Assist in the process of executing clinical trial and vendor agreements

Assist with study document filing

Knowledge Management / People Management

In support of goals, the Clinical Trial Assistant will :

Assist in updating SOPs

Support GCP and operational systems training

REQUIRED QUALIFICATIONS / EXPERIENCE (BASIC QUALIFICATIONS) :

Bachelor's Degree in a Life Sciences

Minimum of 3 years experience in clinical operations methods and processes in industry setting required

At least 2 years oncology monitoring experience preferred

Strong understanding of ICH, GCP, and relevant regulatory requirements

Good communication skills and proficiency with Microsoft Outlook, Excel, Word and PowerPoint

Familiarity with setting up and maintaining trial master files and performing file audits preferred

Proactive and able to work independently

Ability to prioritize and multi-task with attention to detail

Strong organizational skills

About AVEO

AVEO is a commercial-stage, oncology-focused biopharmaceutical company committed to delivering medicines that provide a better life for patients with cancer. AVEO currently markets FOTIVDA (tivozanib) in the U.S. for the treatment of adult patients with relapsed or refractory renal cell carcinoma (RCC) following two or more prior systemic therapies. AVEO continues to develop FOTIVDA in immuno-oncology combinations in RCC and other indications, and has several other investigational programs in clinical development. AVEO is committed to creating an environment of diversity, equity and inclusion to diversify representation within the Company.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.