At a Glance
- Tasks: Lead innovative clinical projects and drive new developments in assessment technologies.
- Company: Join a global CRO dedicated to improving lives through pioneering clinical research.
- Benefits: Remote work, diverse environment, and opportunities for professional growth.
- Other info: Collaborative culture that values creativity and inclusivity.
- Why this job: Make a real impact on patient outcomes while working with a passionate team.
- Qualifications: Master’s degree in life sciences and 10 years of clinical trial experience required.
The predicted salary is between 80000 - 100000 £ 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.
Why Worldwide: we believe everyone plays an important role in making a world of difference for patients and their caregivers. We prioritize a diverse and inclusive environment that promotes 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.
What The Clinical Assessment Technologies Department Does: At Worldwide Clinical Assessment Technologies (CAT) is a team of highly experienced clinicians and operations experts whose purpose is to improve clinical outcomes data by reducing data variability associated with lack of training, inconsistent approaches to scale administration and scoring, placebo response, and incorrect source. The CAT team has conducted more than 75 international Phase I to Phase IV trials and has trained over 7,000 raters.
Responsibilities:
- Engages with senior management to establish strategic department initiatives and objectives.
- Drive new QMD developments, including authoring and reviewing QMD documents and guidance documents.
- Active participant in the identification and development of new service arms, and in the improvement of existing service arms.
- Drive business development activities for CAT, including proposals input, participation in capabilities and bid defense activities.
- Identify clinical needs for upcoming and current projects, track and review with CAT Clinical Staff and CAT Leadership.
- Accountable for the development of assessment training content and plans by ensuring the training curriculum and materials (including training videos) meet protocol, copyright holder, author, and sponsor requirements.
What You Will Bring To The Role:
- Strong organizational skills, detail- and service-oriented, with excellent management skills.
- Strong understanding of best business practices with respect to rater training, methodologies, and corporate discipline.
- Personality focused on meeting timelines consistently and being able to effectively work under pressure.
- Excels in writing and verbal communication skills in order to clearly and concisely present information.
- Ability to handle multiple tasks and many administrative details in a fast-paced and constantly changing environment.
- Clear ability to proactively identify and escalate potential project issues to appropriate CAT and Worldwide staff.
- Strong proficiency in all MS-Office applications including Microsoft Word, Excel, Teams, and PowerPoint.
Your Experience:
- Minimum of earned Master’s Degree in life sciences or equivalent.
- At least 10 years clinical trial experience with clinical assessments, independently organizing and conducting projects, and presenting at Investigators’ Meetings or similar presentations as expert clinicians.
- Preferred at least 4 years of experience managing team members or providing direct clinical mentorship.
- Strong applied knowledge of pivotal efficacy measure administration conventions that can be used in the administration and review of such instruments and communicated to train assessors.
- Knowledge of operational aspects regarding Phase I-IV clinical research trials and experience working with a Contract Research Organization/Rater Training Organization.
- Excellent collaborative skills and ability to work cross-functionally to drive projects and initiatives.
- Strong ability to apply knowledge and utilize available resources to develop new ideas and improve existing processes.
- Excellent knowledge of SOPs, ICH/GCP/regulatory guidelines.
- Competent working with data and numbers.
- Willingness to travel.
We love knowing that someone is going to have a better life because of the work we do.
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.
Director of Clinical Projects, Clinical Assessment Technologies - Europe - Remote in England employer: Worldwide Clinical Trials
At Worldwide Clinical Trials, we are not just a global CRO; we are a community of innovators dedicated to improving lives through our pioneering work in clinical research. Our remote work culture fosters collaboration and creativity, allowing you to thrive while making a meaningful impact on patient outcomes. With a commitment to diversity and inclusion, we offer exceptional growth opportunities and a supportive environment where your contributions are valued and recognised.
We think you need these skills to ace Director of Clinical Projects, Clinical Assessment Technologies - Europe - Remote in England
Some tips for your application 🫡
Show Your Passion:When writing your application, let your passion for improving lives shine through. We want to see how your values align with our mission at Worldwide Clinical Trials.
Tailor Your CV:Make sure to customise your CV to highlight relevant experience in clinical trials and project management. We love seeing how your unique background fits into our innovative team!
Be Clear and Concise:Use clear and concise language in your application. We appreciate strong communication skills, so make sure your writing reflects that by getting straight to the point.
Apply Through Our Website:Don’t forget to apply through our careers page! It’s the best way for us to receive your application and ensures you’re considered for this exciting opportunity.
How to prepare for a job interview at Worldwide Clinical Trials
✨Know Your Stuff
Make sure you have a solid understanding of clinical trial processes and the specific methodologies used in clinical assessments. Brush up on your knowledge of ICH/GCP guidelines and be ready to discuss how you've applied these in your previous roles.
✨Showcase Your Leadership Skills
As a Director, you'll need to demonstrate your ability to manage teams effectively. Prepare examples of how you've mentored team members or led projects, highlighting your collaborative approach and how you’ve driven initiatives to success.
✨Be Ready for Scenario Questions
Expect questions that assess your problem-solving skills in real-world scenarios. Think about past challenges you've faced in clinical projects and how you navigated them. This will show your ability to handle pressure and meet timelines.
✨Communicate Clearly
Your writing and verbal communication skills are crucial for this role. Practice articulating complex information clearly and concisely. You might even want to prepare a brief presentation on a relevant topic to showcase your communication prowess during the interview.