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:

As a Senior Associate/Specialist Document Coordinator, you will support the Global Medical Writing Team to deliver its portfolio effectively and efficiently. This role involves managing the quality review of clinical and regulatory documents Conducting quality review of clinical and regulatory documents, including Protocols, Clinical Study Reports, Briefing Books, Investigator Brochures, Clinical Summary documents, PBRER, DSUR, and RMP.

 

Who You Are:

 

Minimum Requirements:

 

A graduate or postgraduate degree in a relevant field such as BPharm, MPharm, BDS (Dental), BSc, MSc, MD, or PhD, or an equivalent combination of job experience.Excellent written and spoken English, including medical terminology.2-5 years of experience in the pharmaceutical industry with relevant scientific and regulatory knowledge.Knowledge of ICH/Good Clinical Practices, CTD guidance, and GVP guidance.

 

Preferred Requirements:

 

Conducting quality review of clinical and regulatory documents, including Protocols, Clinical Study Reports, Briefing Books, Investigator Brochures, Clinical Summary documents, PBRER, DSUR, and RMP.Participating in meetings related to medical writing, quality control, and compliance activities.Collaborating cross-functionally to continuously improve medical writing processes.Familiarity with the AMA style guide.A flexible attitude with respect to work assignments and new learning; readily adapt to changes.Experience working within a team in a collaborative and supportive role.

 

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!