Global Medical Information & Safety Specialist

IQVIA; Barcelona; On-site; EUR 27,000 - 40,000; Full time

Job summary

IQVIA in Spain seeks a Medical Information Specialist to deliver high-quality medical information to healthcare professionals, patients and consumers across multiple channels. You will provide accurate, balanced, non-promotional information and support safety reporting activities.

You will identify adverse events, document product quality complaints, and collaborate with Pharmacovigilance, Quality and cross-functional teams to ensure compliance and continuous improvement.

Qualifications

• Bachelor's degree in Life Sciences, Pharmacy, Nursing, Medicine, or a related field.
• Excellent written and verbal communication in Lithuanian and English; other languages a plus.
• Strong scientific aptitude and ability to communicate medical information.
• Understanding of adverse event reporting and pharmacovigilance principles.
• Ability to manage multiple priorities and collaborate with cross-functional teams.

Responsibilities

• Respond to medical and product-related inquiries via phone, email and other channels.
• Provide accurate, evidence-based medical information on products and therapies.
• Document customer interactions per company procedures.
• Use approved medical information resources and literature to address inquiries.
• Identify and route adverse events and product quality complaints.
• Support safety data intake and documentation in designated systems.
• Collaborate with Medical Information, Pharmacovigilance, Quality and other teams.
• Participate in training, quality initiatives, and continuous improvement.

Skills

Multilingual communication

Attention to detail

Organizational skills

Interpersonal skills

Team collaboration

Pharmacovigilance knowledge

Education

Bachelor's degree in Life Sciences, Pharmacy, Nursing, Medicine, or another relevant scientific discipline

Job description

IQVIA in Spain seeks a Medical Information Specialist to deliver high-quality medical information to healthcare professionals, patients and consumers across multiple channels. You will provide accurate, balanced, non-promotional information and support safety reporting activities.

You will identify adverse events, document product quality complaints, and collaborate with Pharmacovigilance, Quality and cross-functional teams to ensure compliance and continuous improvement.