Real World Evidence Trainee - 12 month Career Starter Program

Real World Evidence Trainee, a member of Country Medical Affairs Team responsible for scientific evidence & data generation plans & activities across therapeutic areas and along product life cycle. RWE Trainee will be responsible for operational and administrative support in developing and implementing the Country Medical Affairs product-related scientific data generation plan & vision.
Job Responsibilities  
Set up and ensure access is provided to the study team to all systems and tools required for the management of the study 
Set up, maintenance and accurate periodic update of study information in the Clinical Trial Management System (CTMS)  
Set up and maintenance of study contact lists 
Set up and maintenance of Issue Action and Decision Log and FAQ log 
Assist with the administration task of the studies  
Drafts and/or assists with the preparation and tracking of trial-related documents, tools and templates  
Support planning and logistics for meetings to include internal and external meetings. 
Actively take part in study meetings and be responsible for the meeting minutes during the call. 
Generate, finalize, and distribute meeting agenda and meeting minutes 
Prepare, contribute to and distribute presentation material for meetings and newsletters 
Management of invoice tracker and support with financial reconciliation 
Maintain the study master file 
Coordinate and distribute study supply as deemed necessary 
Prepare, execute, track, collect, review study documents and ensure their completeness according to external guidelines and AstraZeneca SOPs 

Typical Accountabilities
  
Support execution end to end preparation, delivery and dissemination of the AZ generated evidence 
Conduct activities and interactions consistent with Company values and in compliance with the Code of Conduct and supporting Policies and Standards relevant to your role. Complete all required training on the AZ Code of Conduct and supporting Policies and Standards on time. Report potential issues of non-compliance.  
Ensures appropriate tracking of milestones for AZ studies, compliance with reporting requirements and budget spend 
Ensures and monitor compliance by project team members and third parties by (a) positively reinforcing the Code of Conduct and all relevant AstraZeneca Policies and Standards, (b) ensuring completion of all required training, and (c) immediately addressing and reporting, as appropriate, instances of non-compliance.  
Accountability for GXP areas is expected.  
 
Requirements:
Essential 
University degree / last 1-2 years of studies (preferably in life-science – medicine, pharmacy, other) 
focus on development enthusiasm and passion 
being a kind of “fast-learner” 
attention to details 
willingness to take on new challenges and contribute in the form of your own unique ideas and skills 
analytical thinking  
Desirable 
operational experience in clinical trials 
experience in writing scientific publications 
 

Date Posted
03-lis-2026
Closing Date
30-lis-2026

AstraZeneca embraces diversity and equality of opportunity.  We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.  We believe that the more inclusive we are, the better our work will be.  We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.  We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.