We are seeking a detail-oriented and analytical professional to join our team as a Medical Information Specialist. In this role, you will be responsible for addressing medical information requests from multiple programs using approved response documents.
Key Responsibilities:
* Process and document medical information requests according to company procedures and project working practices.
* Identify and document adverse events, product complaints, and quality issues according to company procedures.
* Report AE information to the pharmacovigilance department.
* Collaborate with internal teams for scientific support as needed.
* Participate in product training and provide support on report clarification, metrics, volumes, KPIs, and compliance investigations.
* Evaluate L2 medical information requests according to project agreement.
* Support internal and external audits.
* Perform quality control of medical information requests to ensure adherence to project requirements.
Requirements and Qualifications:
* Bachelor's degree in a relevant field.
* Basic knowledge of pharmaceutical industry regulations.
* Excellent computer skills and proficiency in MS Office.
The ideal candidate will possess excellent communication and organizational skills, with the ability to work independently and collaboratively as part of a team. They will also have strong analytical and problem-solving skills, with attention to detail and the ability to multitask.