At a Glance
- Tasks: Manage RTSM projects, ensuring timely delivery and quality standards.
- Company: Join a global CRO dedicated to innovative healthcare solutions.
- Benefits: Inclusive culture, career growth, and the chance to make a real impact.
- Other info: Dynamic workplace fostering creativity and collaboration.
- Why this job: Be part of a mission-driven team improving lives through clinical trials.
- Qualifications: Degree or equivalent experience with 1+ years in RTSM and CRO environments.
The predicted salary is between 35000 - 45000 € per year.
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 year 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.
We love knowing that someone is going to have a better life because of the work we do.
RTSM Associate - UK/Europe employer: Worldwide Clinical Trials
At Worldwide Clinical Trials, we pride ourselves on being a dynamic and inclusive employer that empowers our employees to make a meaningful impact in the world of clinical research. Our supportive work culture fosters collaboration and creativity, while our commitment to professional development ensures that every team member has the opportunity to grow and thrive in their career. Join us in our mission to improve lives and experience the unique advantages of working in a global, midsize CRO that values innovation and excellence.
StudySmarter Expert Advice🤫
We think this is how you could land RTSM Associate - UK/Europe
✨Tip Number 1
Network like a pro! Reach out to current or former employees at Worldwide Clinical Trials on LinkedIn. A friendly chat can give you insider info and maybe even a referral, which can really boost your chances.
✨Tip Number 2
Prepare for the interview by knowing your stuff! Research RTSM topics and be ready to discuss how your experience aligns with the role. Show us that you're not just a fit on paper but also in passion and purpose.
✨Tip Number 3
Practice your communication skills! Since this role requires effective client-facing abilities, consider doing mock interviews with friends or using online platforms to refine your pitch and responses.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re genuinely interested in joining our team at Worldwide.
We think you need these skills to ace RTSM Associate - UK/Europe
Some tips for your application 🫡
Tailor Your Application:Make sure to customise your CV and cover letter for the RTSM Associate role. Highlight your relevant experience in project management and any specific RTSM knowledge you have. We want to see how your skills align with our mission!
Showcase Your Communication Skills:Since effective communication is key in this role, use clear and concise language in your application. We love candidates who can express their thoughts well, so don’t hold back on showcasing your written communication prowess!
Highlight Your Team Spirit:We’re all about collaboration here at Worldwide. Make sure to mention any experiences where you’ve worked successfully in a team environment. We want to know how you contribute to a positive team dynamic!
Apply Through Our Website:Don’t forget to submit your application through our careers page! It’s the best way for us to receive your details and ensures you’re considered for the role. We can’t wait to see what you bring to the table!
How to prepare for a job interview at Worldwide Clinical Trials
✨Know Your RTSM Inside Out
Make sure you brush up on your knowledge of RTSM topics, including study design and randomisation methodologies. Being able to discuss these concepts confidently will show that you're not just familiar with the basics but are genuinely interested in the role.
✨Showcase Your Communication Skills
Since this role involves a lot of client-facing interactions, practice articulating your thoughts clearly and concisely. Prepare examples of how you've effectively communicated complex information in previous roles, as this will demonstrate your ability to engage with stakeholders.
✨Demonstrate Problem-Solving Abilities
Think of specific instances where you've successfully troubleshot issues or improved processes. Be ready to share these examples during the interview, as they highlight your initiative and creativity—qualities that Worldwide values highly.
✨Emphasise Team Collaboration
Worldwide is all about teamwork, so be prepared to discuss how you've contributed to team success in the past. Share stories that illustrate your ability to work well with others, adapt to new technologies, and support your colleagues in achieving common goals.
