If you are looking to jump-start your career in drug development / clinical trials in a full-time, salaried position, that not only allows you to learn and grow on the job, but also includes a complimentary, highly acclaimed and tailored course curriculum, you should read on!

This is an entry level position designed to thoroughly train you to develop into an independent Clinical Research Associate . Our global Monitoring Excellence Academy (MEA) program consists of multiple theoretical and practical components, such as foundations trainings, observational training visits and blended instructional content.

For the duration of your MEA training, you will be a part of our Munich-based team of specialized Clinical Trial Coordinators, working directly with one of our most important sponsors and advancing the development of innovative medications for a variety of therapies and gaining practical experience with various business processes around clinical trials at the same time.

Typical day to day Coordinator tasks include:

• Prepare, update, record, collate, distribute, archive and dispose of documents (electronic and physical files)
  
• Be responsible for document processing to electronic Trial Master File (eTMF)
  
• Be involved in validation activities
  
• Distribute and track safety reports (SUSARs)
  
• Be responsible for site invoice requests and invoice processing
  

Aside from our MEA training program, we offer you:

• work as part of a diverse and stable team
  
• in-depth Onboarding, including personal support from your mentor
  
• flexible working hours, capped overtime and compensatory time off in lieu
  
• a permanent employment contract
  
• travel time = work time
  
• highly competitive compensation packages includingChristmas and vacation allowances
  
• regular, merit-based salary adjustments
  
• significant employer contributions to an attractive pension scheme
  
• excellent training and career development opportunities
  
• strong support from Line Management and more than 20'000 colleagues worldwide
  
• the world's most renowned pharmaceutical companies as our satisfied, repeat customers for many years
  

Your profile:

• degree in a relevant field such as life sciences, (veterinary) medicine, pharmacology, biology, chemistry, health care, health management, nursing etc.
  
• in lieu of the above, a completed vocational education or professional experience (e.g. as study nurse, study coordinator) in a relevant field
  
• first professional experience in clinical research / drug development
  
• basic understanding of biology and biological processes
  
• familiarity with and/or practical application of ICH guidelines and GCP
  
• proficient user of IT applications such as MS Office and possibly even clinical software - e.g. study databases, eTMF (Veeva Vault)
  
• solid organizational and project management skills with a keen attention to detail and a high sense of accountability
  
• excellent communication skills in business fluent German and English - verbal and written - and strong interpersonal skills are a must
  

Labcorp is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.

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