Medical Information Specialist

AmerisourceBergen

España

On-site

EUR 28,000 - 42,000

Full time

7 days ago
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Benefits offered by this job

Full time
Affiliated Companies: PharmaLex Spain

Job summary

AmerisourceBergen in Spain seeks a German-speaking Medical Information Specialist to handle MIR requests from multiple programs, documenting responses per procedures and collaborating with regulatory and medical affairs teams. The role offers remote work within Spain or based at the Madrid office.

A life sciences background and fluency in German, Spanish, and English are highly valued. The position emphasizes accuracy, cross-functional collaboration, and compliance with project requirements,

Qualifications

  • Bachelor's degree in life sciences, pharmacy, biomedical sciences, public health, or related field.

Responsibilities

  • Address Medical Information requests (MIR) from multiple programs and sources using approved response documents.
  • Ensure MIR are processed and documented according to procedures and project working practices.
  • Identify and document adverse events (AE), product complaints, and quality issues per procedures.
  • Report AE information to pharmacovigilance.
  • Collaborate with internal teams (regulatory, medical affairs, marketing) to provide scientific support.
  • Participate in client product training and therapeutic area education as required.
  • Support project team with reports, metrics, volumes, KPIs and investigations.
  • Escalate MIR (L2) as per project agreement.
  • Support in internal and external audits.
  • Perform quality control of MIR to ensure adherence to requirements.

Skills

Spanish
German
English

Education

Bachelor's degree in life sciences

Job description

Job Details

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. It's an exciting opportunity to join our global consulting service. If you don't 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 ,

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 client's internal teams, including regulatory, medical affairs and marketing to provide scientific support as needed.
  • Participate in client's 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.
Education

Education: Bachelor's degree in life sciences, pharmacy, biomedical sciences, public health, or a related field, or equivalent experience required.

Certifications

Certification in clinical research or regulatory affairs preferred.

Certification in data analytics or scientific data interpretation tools preferred.

Experience

Experience: Less than 2 years of experience in scientific consulting, healthcare, life sciences, or a related field required.

Skills

Skills: Required proficiency in Spanish, English and German language.

What Cencora offers
  • 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 time
  • Affiliated Companies: PharmaLex Spain S.L.U.
Equal Employment Opportunity

Cencora 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 company's 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.

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