RTSM Associate - UK - 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 Systems 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 for amendments, including oversight and accountability of deliverables and timelines and completion of work to Worldwide SOP standards Communicates information on applicable RTSM project activities to stakeholders, including internal and sponsor study teams Serves as the escalation point of contact during RTSM study maintenance Troubleshooting RTSM issues and drives through to resolution Prepare, review and approve site and support materials as well as helpdesk documentation, when required Perform QC checks of manual database edits and other tasks where required What you will bring to the role Ability to communicate concisely and effectively in both written and spoken English Proficient client-facing skills Proficient in the use of common office software Self-motivated individual who can positively contribute to a team environment High attention to detail with the ability 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 Your experience Educated to degree level in a relevant discipline or able to demonstrate equivalent experience Minimum 1 years prior RTSM experience Minimum of 2 years experience within CRO /pharma environment Contract Research Organization (CRO) or Pharmaceutical experience required Familiar with RTSM topics, including RTSM study design, randomization methodologies, and just-in-time drug supply Understanding of clinical trials, blinding, patient safety, data integrity and associated regulations Proven ability to manage delivery of RTSM solutions deployed in clinical trials We love knowing that someone is going to have a better life because of the work we do. To view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn. Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law. This is who we are. We’re a team of clinicians, scientists, and researchers who want to make healthcare better. We were founded on an unwavering commitment to authentic, personalized attention. And today, as CROs consolidate and the industry changes rapidly, that personalized attention is more important than ever. We all came to this industry for different reasons, from different walks of life. If you ask any one of us why we’re here, you’ll get a different answer. And that’s what makes us special. Not finding the right fit? 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