Senior Specialist - Clinical Trial Coordinator

Work Your Magic with us!

Ready to explore, break barriers, and discover more We know you've got big plans – 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.

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

Your Role

In this role, you will coordinate clinical trial support activities that help teams deliver accurate and compliant study operations. Reporting to the Head of Local-Regional Studies Support Office, you will reconcile Trial Oversight Plans, maintain safety and trial team records, support quality reviews, track budgets and invoices, and coordinate transparency and vendor data. You will work with clinical development colleagues, contributing functions, vendors, contract research organizations and investigators, improve processes and manage your work independently with moderate guidance.

Who You Are

• Bachelor's degree in a scientific field or equivalent experience, with 5 to 8 years in clinical research or Clinical Development.
• Working knowledge of clinical operations, medical and trial terminology, and International Council for Harmonisation Good Clinical Practice.
• Experience coordinating clinical trial records, quality reviews, safety distribution lists, clinical milestone data and vendor information.
• Experience with study budget tracking, invoice processing, goods receipts and accruals using finance or procurement systems.
• Clear written and verbal communication, with confidence working across international, multicultural teams and with vendors, contract research organizations and investigators.
• Organized, accurate and discreet, with strong time management, prioritization, multitasking, problem solving and critical thinking skills.
• Able to take initiative, work independently with moderate guidance, collaborate effectively and support the training or onboarding of new staff.
  
  

Location: Bangalore, India | Office based and hybrid

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety 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!

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!