.Diverse Minds.
Go further with bold new opportunities: Collaborate in an inclusive environment, a place full of bold new opportunities.
We're looking for people who are open and respectful, ambitious and driven.
Who we are: Passion, determination, and resilience is in our DNA.
That's why we always step up, never afraid to learn from our failures.
What we do: We work independently or in partnerships to deliver the next wave of science and address unmet medical needs.
Why we love it: You will be valued.
Not only for your unique contribution, skills, and background, but because we recognize people are our greatest asset.
Here we are dedicated to being a Great Place to Work.
We have an exciting opportunity as a Global Development Scientist to join our team within Late Respiratory and Immunology (R&I) Clinical Development.
This role can be based in Barcelona (Spain), Durham (US), Gaithersburg (US), Gothenburg (SE), or Warsaw (Poland).
If your passion is science and you want to be part of a team that makes a bigger impact on patients' lives, then there's no better place to be.
The role: As a Global Development Scientist, you will provide scientific and clinical input to all aspects of late-stage product development.
This includes but is not limited to the design, delivery, and interpretation of pivotal clinical trials and studies that further characterize the overall benefit, risk, and value of products in the Respiratory and Immunology Therapeutic Area (TA) in late-stage development.
You will ensure that the safety evaluation process for clinical trials is seamless and complete.
In this role, you will seek input from the appropriate functional specialists and coordinate activities in support of clinical studies and programs.
Your objectives will be set by the Group Director in agreement with the Global Clinical Head(s).
You will work in close collaboration with the study team physician and other partners with all aspects of scientific input, clinical data quality, and safety evaluation.
What you'll do: Provide scientific contribution in the innovative design, execution, and interpretation of clinical trials in one or more late-stage (Ph2b - Ph3) clinical programs.
Participate in activities that ensure quality, consistency, and integration of clinical study-related deliverables and ensure safety evaluation process within the clinical team.
Provide expert scientific input and collaborate with colleagues in other functions including Patient Safety, Regulatory Affairs, Clinical Operations, and early development groups.
Provide scientific analysis and interpretation of data from ongoing studies and in the literature.
Support and contribute to medical monitoring of trials (safety and efficacy).
Develop and review protocols, informed consent, and investigator's brochure.
Assist in planning for and participate in investigator meetings.
Ensure scientific input to TA standards.
Essential for the role: Science degree (e.G