Associate eCOA Manager - US - Remote

Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way. Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit. Why Worldwide We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us! What the Clinical   System s   Department does at Worldwide   Our Clinical Systems Department plays an essential role for the entire organization by ensuring our systems are developed to study specifications, fully integrated, optimally running, and well-maintained throughout the studies’ lifecycle. The department works closely with industry specific systems such as: IRT, RTSM, EDC, RBQM   Opra ,   ClinSpark ,   eTMF   and CTMS. The department has various roles including client-facing Project Managers, System and Software Designers, and Implementation and Validation specialists. Each of these areas provides mentorship and training. In working with a variety of systems, the department has a proven record of success for promotions and growth internally.   What you will do   Provide project management oversight from maintenance to   eCOA   decommissioning, including oversight and accountability of deliverables and timelines and completion of work to Worldwide SOP standards   Review and   identify   study trends and proactively work with   eCOA   vendor and study team to address study specific requirements   Communicate information on applicable   eCOA   project activities to stakeholders, including internal and sponsor study teams. Serves as the escalation point of contact for all   eCOA   assigned study-related project issues   Overall accountability for coordination and   timely   delivery of   eCOA   project communications including study status reports, meeting agendas and minutes and scheduling project calls   Responsible for overall   eCOA   study design review and approving User Requirements Specification (URS) for post go-live Change in Scope   Prepare,   review   and approve site and support materials as well as helpdesk documentation, when   required   Perform financial review and budget management, including review of Change Orders   What you will bring to the role   Ability to communicate concisely and effectively in both written and spoken English   Proficient client-facing skills   Self-motivated individual who can positively contribute to a team environment   with the a bility to prioritize and handle multiple projects simultaneously   Flexible and able to use sound independent judgment and take initiative to assess information   Able to make effective decisions in a fast-paced, highly dynamic environment   Able to be creative, adapt to   new technologies , concepts and processes, make   improvements   and solve problems Highly organized, detail- and service-oriented   Excellent project management skills   Your experience   Educated to degree level in a relevant discipline or able to demonstrate equivalent experience   Minimum 1 year   of experience working in   eCOA   and clinical trials Minimum 1 year of experience in project management The individual must demonstrate   an ability   to lead, understand policies and procedures, financial and leadership principles, possesses excellent time management and project management skills and communicate effectively.   Demonstrable knowledge of operational aspects   regarding   Phase I-IV clinical research trials     Has knowledge of the Software Development Life Cycle (SDLC) and be familiar with   eCOA   topics, including   eCOA   designs and scales Contract Research Organization (CRO) or pharmaceutical experience   required   Fluency in English (will be   required   to write, speak, and understand English to conduct day-to-day business) The role may require travel domestically and internationally   in order to   attend key meetings. The global nature of the position may also require the incumbent to occasionally manage their time flexibly   in order to   be responsive to stakeholders in different time zones.   At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation. The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates): United States of America - $71,500.00 - $142,500.00 The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it not a guarantee of exact salary. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage. We love knowing that someone is going to have a better life becaus