Cielianna L. Email & Phone Number

Hackensack, New Jersey, United States

Union, New Jersey, United States

Mississauga, On

• Coordinate internal and external resources for flawless execution of each study from start-up to close-out• Establish and maintain relationships with sites, sponsors, & third party vendors; act as liaison between groups as primary point of contact• Develop project timelines and budget, and essential documents such as protocol, informed consent form, and clinical trial application• Create detailed project plans to track and maintain steady progress in line with budget and… Show more • Coordinate internal and external resources for flawless execution of each study from start-up to close-out• Establish and maintain relationships with sites, sponsors, & third party vendors; act as liaison between groups as primary point of contact• Develop project timelines and budget, and essential documents such as protocol, informed consent form, and clinical trial application• Create detailed project plans to track and maintain steady progress in line with budget and timelines• Perform site monitoring and management activities including site visits and report writing• Lead weekly meetings with cross-functional project teams, including kick-off meeting at start-up and data review and lessons learned at close-out• Create, maintain, and distribute regular study status reports to internal and external stakeholders• Contribute to the development of department and company-wide Standard Operating Procedures (SOPs) Show less

Mississauga, On

• Establish and maintain tracking systems and tools and report study metrics to sponsors• Prepare, track, and distribute pertinent project documents and status reports to sites, vendors, and sponsors• Lead study start-up activities, including site identification and feasibility• Initiate meeting topics and agendas, create study specific references, and record detailed minutes• Review Informed Consent Forms and Confidentiality Agreements for content and clarity• Prepare study… Show more • Establish and maintain tracking systems and tools and report study metrics to sponsors• Prepare, track, and distribute pertinent project documents and status reports to sites, vendors, and sponsors• Lead study start-up activities, including site identification and feasibility• Initiate meeting topics and agendas, create study specific references, and record detailed minutes• Review Informed Consent Forms and Confidentiality Agreements for content and clarity• Prepare study documents and complete submissions to Ethics and Regulatory boards in Canada and USA• Manage clinical documentation and ensure Trial Master File is accurate and inspection-ready at all times Show less

Mississauga, On

• Manage and maintain Trial Master File according to DIA reference model throughout project lifecycle• Contribute to the development of study documents for Ethics and Regulatory submissions• Assist with design, planning, and implementation of clinical trials• Assist with preparation for regulatory and/or sponsor audits• Report AEs and SAEs to ethics and regulatory boards

Mississauga, On

• Recruit qualified candidates for all clinical trials and schedule visits within allotted projected timelines• Enter relevant patient and clinical information into study database and case report forms• Create study statistic spreadsheets to analyze data of study statistics, increasing candidate recruitment• Monitor, analyze, and maintain recruitment database, increasing trial productivity • Consolidate multiple trials and studies, resulting in an efficient and increased… Show more • Recruit qualified candidates for all clinical trials and schedule visits within allotted projected timelines• Enter relevant patient and clinical information into study database and case report forms• Create study statistic spreadsheets to analyze data of study statistics, increasing candidate recruitment• Monitor, analyze, and maintain recruitment database, increasing trial productivity • Consolidate multiple trials and studies, resulting in an efficient and increased candidate recruitment Show less

Newark, Nj

Newark, Nj

Received full athletic scholarship, 4 year starterVoted captain senior year by fellow teammatesOrganized a group of 20+ girls in practice and game environmentHeld weekly meetings with the coaching staff to discuss team developmentHead of team Leadership Council

Newark, Nj

Performed multiple hours of service to the school, community, and nation, working on projects such as park and beach cleanups, building homes with Habitat for Humanity, and working at food banks.Organized weekly fellowship events for the brotherhood.Held weekly meetings with a committee to plan various fellowship events

Master Of Science (M.S.), Bioengineering And Biomedical Engineering

Activities and Societies: Alpha Phi Omega

Bachelor Of Science (B.S.), Bioengineering And Biomedical Engineering

Activities and Societies: Women's Soccer, Alpha Phi Omega