Medical Information Specialist
Job Summary
Our team members are at the heart of everything we do. At Cencora we are united in our responsibility to create healthier futures and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health come join our innovative company and help us improve the lives of people and animals everywhere. Apply today!
We are looking for a talented German- speaking Medical Information Specialist in Spain. This role can be remote in Spain or if you prefer you can be based from our Madrid office. Its an exciting opportunity to join our global consulting service.
Dont meet the full experience requirement We still encourage you to apply. If you dont yet have the experience we would still be happy to hear from you. We are open to training the right candidate and will consider applicants with an educational background in pharmacy or healthcare who are eager to learn and grow in the role. If you meet the language requirements in German Spanish and English we encourage you to submit your application.
Responsibilities:
-Address Medical Information requests (MIR) from multiple programs and sources using approved response documents.
-Ensure that all the MIR are processed and documented according to Organization and client procedures and project working practice.
-Identify and document adverse events (AE) product complaints and quality issues according to Organization and clients procedures.
- Report AE information to the pharmacovigilance department.
-Collaborate with Organization and clients internal teams including regulatory medical affairs and marketing to provide scientific support as needed.
-Participate in clients product training diseases and therapeutic areas as per project requirement.
-Support project team on any report clarification metrics volumes KPIs and compliance investigations.
-Escalate L2 MIR as per project agreement.
-Support in internal and external audits.
-Perform quality control of MIR to ensure adherence to project requirements and procedures.
-Reconcile medical information reports with adverse events and product quality complaint reports within the agreed timelines.
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Education:
-Bachelors degree in life sciences pharmacy biomedical sciences public health or a related field or equivalent experience required.
-Certification in clinical research or regulatory affairs preferred. Certification in data analytics or scientific data interpretation tools preferred.
Experience:
-Less than 2 years of experience in scientific consulting healthcare life sciences or a related field required.
Skills:
-Required proficiency in Spanish English and German language
Benefit offerings outside the US may vary by country and will be aligned to local market practice. The eligibility and effective date may differ for some benefits and for team members covered under collective bargaining agreements.
Full timeCencora is committed to providing equal employment opportunity without regard to race color religion sex sexual orientation gender identity genetic information national origin age disability veteran status or membership in any other class protected by federal state or local law.
The companys continued success depends on the full and effective utilization of qualified individuals. Therefore harassment is prohibited and all matters related to recruiting training compensation benefits promotions and transfers comply with equal opportunity principles and are non-discriminatory.
Cencora is committed to providing reasonable accommodations to individuals with disabilities during the employment process which are consistent with legal requirements. If you wish to request an accommodation while seeking employment please call 888.692.2272 or email . We will make accommodation determinations on a request-by-request basis. Messages and emails regarding anything other than accommodations requests will not be returned
Required Experience:
IC
About Company
Discover how Cencora delivers innovative cell and gene therapy solutions, enhancing patient access, affordability, and connectivity across treatment journeys.