I have been working in clinical research for over 20 years in a variety of positions including coordinator, CRA, project manager, CRA manager and site liaison specialist. I have been fortunate to work with a variety of companies focusing on a variety of therapeutic areas including vaccines and oncology. I am moving into contract work effective immediately. I enjoy a site facing role and travel to research sites.

• Establish productive working relationships with clinical partners at major healthcare organizations and community research centers• Assist in the identification and assessment of potential Strategic Master Site partners to align with the clinical development strategy• Administer and review Master Site feasibility questionnaires• Conduct Strategic Master Site clinical site evaluation and pre-study visits of potential investigators to evaluate the capability of the site to successfully conduct clinical studies• Collaborate with the Strategic Partnerships team to develop and manage Strategic Master Site advisory groups, produce site communications, and coordinate ongoing engagement with Master Strategic Site partners• Represent EQRx professionally when engaging with internal and external partners• Produce thorough, accurate and timely reports of project activities• Liaise with in-house teams to facilitate and problem solve site/CRO issues

• Established productive working relationships with clinical partners at major healthcare organizations to support EQRx’s goal of bringing innovative medicines to patients at a fraction of the price• Assisted in the identification and assessment of potential Strategic Master Site partners to align with the clinical development strategy• Administered and reviewed Master Site feasibility questionnaires, managed the collection of essential regulatory documents, and coordinated remote technology integrations• Conducted Strategic Master Site clinical site evaluation and pre-study visits of potential investigators to evaluate the capability of the site to successfully manage and conduct clinical studies• Collaborated with the Strategic Partnerships team to develop and manage Strategic Master Site advisory groups, produce site communications, and coordinate ongoing engagement with Master Strategic Site partners• Represented EQRx professionally when engaging with internal and external partners• Produced thorough, accurate and timely reports of project activities

• Provided strong leadership to a team of 24 FTE and FSP CRAs to meet project timelines and expectations• Reviewed CVs, interviewed CRA and CRA manager candidates• Developed training plans and assured training compliance for all direct reports, including guiding professional development, completing performance reviews and implementing performance improvement plans as necessary• Participated in clinical operations quality or process initiatives, including patient engagement• Responsible for execution of the site management and monitoring function of clinical trials• Performed on-site quality control visits for the CRA team• Assumed monitoring duties as needed to assist the study teams

• Clinical Trial Lead for Phase III influenza vaccine trial with enrollment of 32,000 subjects over a two-year period• Liaison for CRO partnership for clinical operations management, while performing quality control audits and evaluating CRA, physician, and study site performance• Administered vaccine trials to ensure superior quality of work and maximize sites productivity in line with ICH GCP guidelines and Sanofi Pasteur SOPs• Assisted with formulation and execution of site relationship initiative to streamline communication and management of clinical trials between sponsor and site• Spearheaded qualification, initiation, monitoring and close out visits by coordinating with the project team

Responsible for timely monitoring of research sites including quality oversight