About You
At Excelya, taking audacious steps is encouraged , so we’re looking for individuals who are ready to grow with us and share our values. •
Experience:
One or more years as a Data Manager or equivalent combination of education, training and experience •
Skills:
· Knowledge and understanding of ICH GCP and other relevant ICH, EU or FDA guidelines to maintain regulatory compliance · Understanding of recommended CDM best practices and associated documentation · Experience in clinical trial databases and applications, clinical data flow, data review, and eCase Report Form design. · Understanding of clinical trials and study lifecycle (start-up, maintenance & closeout) · Proficient in computer technology used in an office environment (Word, Excel, PowerPoint, MS Project, etc). · Ability to maintain high level of professionalism, ethics and compliance at all times. · Effective verbal and written communication skills •
Education:
- Bachelor’s degree qualification in a Scientific discipline is preferred • Languages: Fluency in English About the Job Join Excelya, where Audacity, Care, and Energy define who we are and how we work.
- We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.
- This role is an exciting opportunity to contribute to a dynamic, ambitious team in Data Management.
- You will play a critical part in driving innovation and making an impact in the clinical research space, while enjoying a stimulating professional environment that encourages personal and intellectual growth.
- The Clinical Data Manager is responsible for performing Data Management tasks per client work orders to high regulatory standards and Excelya Group SOPs. Main Responsibilities · Deeply acknowledges and strictly follows Excelya and Client’s SOPs, guidelines and appropriate local and international legislation. · CDMI works under the supervision of more senior staff (Manager or Senior CDM). · Responsible for data cleaning, data review, discrepancy management and data reconciliation activities on the studies assigned to him/her. · Work closely with the Lead Data Manager responsible for the study. · Generate study metrics and status reports within and across several studies. · Participate to study documentation archiving. · May participates in EDC database build and testing through go live. · Completes Excelya administrative tasks as required e.g., timesheets, CV and training updates. · May undertake other tasks as they may be assigned from the supervisor that will concern any of the Excelya Group companies Why Join Us?
- At Excelya, we combine passion for science with enthusiasm for teamwork to redefine excellence in healthcare.
- Here’s what makes us unique.
- We are a young, ambitious health company representing 900 Excelyates, driven to become Europe’s leading mid-size CRO with the best employee experience .
- Our one-stop provider service model - offering full-service, functional service provider, and consulting - enables you to evolve through diverse projects.
- Working alongside preeminent experts, you will help improve scientific, operational, and human knowledge to enhance the patient's journey.
- Excelling with Care At Excelya, Care lies at the heart of what we do.
- We provide equal opportunities for all and foster a diverse, equitable, and inclusive workplace where humility and boldness work hand in hand.
- Everyone has a space to feel valued, thrive, and collaborate with purpose.
- Your challenges become our shared mission.
- Together, we transform bold ideas into reality, the Excelya way.
- Watch our testimonial video to hear directly from our Excelyates about why Excelya is more than just a workplace—it’s a community built on values.
- Apply today, become an Excelyate!
