RTSM Associate - UK

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.

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.

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.
• Perform QC checks of manual database edits and other tasks.

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.
• 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.

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.