Clinical Research Associate (CRA) - Maternity leave covers
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Ørestad
Clinical Development Centre Denmark (CDC DK)
Ørestad, Denmark
This role is unordinary because it places you at the forefront of groundbreaking clinical research in primarily but not exclusively diabetes and obesity, areas where rapid innovation can directly transform patients’ lives. You’ll not only monitor trials but actively contribute to therapies with the potential to reshape global health outcomes.
Apply today!
We currently have three maternity leave cover positions available: two running for a 7-month period until October 1st, and one lasting until the end of 2026.
Your new role
In this exciting role you will manage clinical trial sites at every stage of the clinical trial process to a high quality in accordance with the company’s policies and procedures, relevant legislation and ICH GCP requirements whilst maintaining the standards of the Way. You will collaborate closely with clinical investigative site teams to deliver our clinical trials according to target. You will be accountable for data integrity, quality, patient safety and protection, regulatory compliance for all assigned sites, compliance to protocols, adherence to Good Clinical Practice, Clinical Trial Legislation, and local ethics requirements, as well as standard operating procedures (SOPs) .
In addition, you will be:
Travel will be required approximately 30% of the time including some overnight stays depending on the clinical site’s location.
Your skills and qualifications
You are a very collaborative team player who is proactive and ready to help in challenging situations. Preferably you got a previous experience of monitoring trials in accordance with ICH GCP methodology as well as healthcare industry knowledge or customer service-based employment.
Moreover, you have the following requirements:
Your new department
Your new department is Clinical Development Centre Denmark (CDC DK). There are currently 19 CRAs across different therapeutic areas who form a strong CRA Team.
We are part of a regional team of 8 countries and work closely with global Trial Managers and Global Trial Portfolio in Head Quarter.
Our department has a very open and honest culture with a fantastic team spirit. We work hard but always find time to have fun together.
Working at
At , we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing, and sales – we’re all working to move the needle on patient care.
What we offer
In addition to a unique and supportive culture, offers strong learning and development opportunities tailored to your career and life stage. Our benefits reflect our commitment to empowering employees to reach their full potential while achieving work-life balance.
Deadline
Please, apply before 6 January 2026
You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV.
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
At we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds, and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
Ørestad, Denmark
This role is unordinary because it places you at the forefront of groundbreaking clinical research in primarily but not exclusively diabetes and obesity, areas where rapid innovation can directly transform patients’ lives. You’ll not only monitor trials but actively contribute to therapies with the potential to reshape global health outcomes.
Apply today!
We currently have three maternity leave cover positions available: two running for a 7-month period until October 1st, and one lasting until the end of 2026.
Your new role
In this exciting role you will manage clinical trial sites at every stage of the clinical trial process to a high quality in accordance with the company’s policies and procedures, relevant legislation and ICH GCP requirements whilst maintaining the standards of the Way. You will collaborate closely with clinical investigative site teams to deliver our clinical trials according to target. You will be accountable for data integrity, quality, patient safety and protection, regulatory compliance for all assigned sites, compliance to protocols, adherence to Good Clinical Practice, Clinical Trial Legislation, and local ethics requirements, as well as standard operating procedures (SOPs) .
In addition, you will be:
- The main line of communication with Investigator site teams
- Conducting and documenting monitoring visits in accordance with the Monitoring Plan and Risk Indicator Reports, using risk-based quality principles
- Driving activities with sites to achieve recruitment and retention targets
- Managing of protocol compliance, IMP handling and data entry requirements at site
Travel will be required approximately 30% of the time including some overnight stays depending on the clinical site’s location.
Your skills and qualifications
You are a very collaborative team player who is proactive and ready to help in challenging situations. Preferably you got a previous experience of monitoring trials in accordance with ICH GCP methodology as well as healthcare industry knowledge or customer service-based employment.
Moreover, you have the following requirements:
- Bachelor's Degree level, life science or nursing qualification or other relevant experience and an excellent understanding of clinical trial procedures – ICH GCP, regulatory issues, SOPs
- GCP Certification
- Knowledge of drug development process
- Good working knowledge of electronic clinical trials systems – Veeva Vault, EDC, IWRS, electronic TMF
- Excellent level of Danish and English
Your new department
Your new department is Clinical Development Centre Denmark (CDC DK). There are currently 19 CRAs across different therapeutic areas who form a strong CRA Team.
We are part of a regional team of 8 countries and work closely with global Trial Managers and Global Trial Portfolio in Head Quarter.
Our department has a very open and honest culture with a fantastic team spirit. We work hard but always find time to have fun together.
Working at
At , we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing, and sales – we’re all working to move the needle on patient care.
What we offer
In addition to a unique and supportive culture, offers strong learning and development opportunities tailored to your career and life stage. Our benefits reflect our commitment to empowering employees to reach their full potential while achieving work-life balance.
Deadline
Please, apply before 6 January 2026
You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV.
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
At we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds, and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
Information og data
Denne ledige stilling har jobtypen "Forretningsudvikler", og befinder sig i kategorien "Kommunikation, marketing, salg".
Arbejdsstedet er beliggende i Ørestad.
Jobbet er oprettet på vores service den 10.12.2025, men kan have været deaktiveret og genaktiveret igen.
- Forretningsudvikler
- Ørestad
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