
Medical Information Specialist
Posted 4 days ago

Posted 4 days ago
This is a fully remote position, open to applicants in Spain.
• Respond to Medical Information requests (MIR) from various programs and sources utilizing authorized response documents.
• Ensure all MIR are managed and recorded in accordance with organizational and client protocols as well as project working practices.
• Identify and log adverse events (AE), product complaints, and quality concerns.
• Relay adverse event details to the pharmacovigilance department.
• Collaborate with internal teams, including regulatory, medical affairs, and marketing, to offer scientific support.
• Engage in client product training, disease understanding, and therapeutic areas as needed for the project.
• Assist the project team with report clarification, metrics, volume tracking, KPIs, and compliance investigations.
• Escalate Level 2 MIR in line with project agreements.
• Aid in internal and external audit processes.
• Conduct quality control of MIR to guarantee compliance with project specifications and protocols.
• Reconcile medical information reports with adverse event and product quality complaint reports within agreed-upon timelines.
• A bachelor's degree in life sciences, pharmacy, biomedical sciences, public health, or a related field, or equivalent experience is required.
• Fewer than 2 years of experience in scientific consulting, healthcare, life sciences, or a related field is necessary.
• Proficiency in Spanish, English, and German is required.
• Certification in clinical research or regulatory affairs is preferred.
• Certification in data analytics or tools for interpreting scientific data is preferred.
• Benefit offerings outside the US may differ by country and will align with local market practices.
• Commitment to equal employment opportunities and non-discriminatory practices in recruiting, training, compensation, benefits, promotions, and transfers.
• Provision of reasonable accommodations during the employment process.
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