Ready to explore, break barriers, and discover more? We know you’ve got big plans – and so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That’s why we are always looking for curious minds that see themselves imagining the unimaginable with us.
Your Role:
As a Clinical Trial Feasibility Specialist, you will be part of the innovative and diverse Operational Design Center (ODC), supporting study and Global Product Teams. Reporting to the Head, Operational Design Center, you will conduct data mining of internal and external databases to develop robust operational strategies for global clinical trials. Your research and analysis will include disease background, current and projected future standards of care, competitive landscape, enrollment benchmarking, and enrollment modeling. You will use site databases and local cross-functional input for study-level operational planning and potential site identification. You will support consistency of deliverables and development of best practices within and beyond the ODC.
Join a strong and diverse team with a variety of professional and personal backgrounds that collaborates transparently with a focus on delivering impact. The ODC is known for its innovation efforts, continuously looking for ways to be more efficient and effective. The work of the ODC informs key decisions made by study teams and senior leaders.
Who You Are:
- Bachelor’s degree in a scientific or business area
- 3+ years of clinical trial feasibility experience supporting data-driven decision making
- Familiarity with relevant operational and feasibility data, applications, and systems used in the pharmaceutical industry
- Excellent analytical and problem-solving skills
- Solid organizational skills, high-quality focus, and result orientation
- Advanced Excel and PowerPoint skills
- Proactively addresses and manages risks and issue escalation
- Ability to work on multiple projects simultaneously
- Experience working with diverse cross-functional and international teams
- Exceptional interpersonal skills, including the ability to communicate clearly and actively contribute to team meetings
- Fluency in English
Responsibilities:
- Research scientific/clinical information, including disease background, current standards of care, and how the proposed intervention fits into the current and projected future treatment landscape.
- Conduct data mining of internal and external databases for developing robust operational strategies for global clinical trials.
- Use site intelligence and local cross-functional input for study-level operational planning and potential site list identification.
- Support consistency of deliverables and development of best practices.
- Identify, analyze, and describe the competing clinical trial landscape to assess trial feasibility.
- Maintain detailed records of work and create and maintain internal libraries and databases.
- Collate results of various analyses into comprehensive reports with tables, graphs, and cited references.
- Participate in intra- and inter-departmental meetings.
- Support the development and evolution of ODC data and analytic capabilities to advance clinical trial operational planning and data-driven decision making.
What We Offer:
We are curious minds from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
