PharmD Jobs at Azurity Pharmaceuticals | Apply Now for Medical Information Manager Role
Are you looking for a career in medical affairs where your expertise can make a meaningful impact on patients’ lives? Azurity Pharmaceuticals, a leader in specialty pharmaceuticals, is hiring a Manager, Medical Information in Hyderabad. In this role, you will support healthcare providers with accurate medical knowledge, contribute to scientific communications, and collaborate with cross-functional teams to ensure the highest standards of quality and compliance.
About the Company
Azurity Pharmaceuticals is a specialty pharmaceutical company committed to delivering innovative, high-quality medications that meet the needs of underserved patients. With a broad product portfolio spanning cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan markets, Azurity has improved the lives of millions of patients worldwide. As part of our Medical Affairs team, the Manager, Medical Information will leverage therapeutic expertise to oversee communications on Azurity products, handle medical information requests from healthcare providers (HCPs), and contribute to cross-functional collaboration.
Job Details
- Job Post: Manager, Medical Information
- Location: Hyderabad, India
- Experience: Minimum of 1+ years of experience in Medical Affairs/Medical Information.
Qualifications:
-
Advanced degree in health sciences (PharmD, PhD preferred). Master’s or Bachelor’s in health sciences (RN, RPh, PA, NP, etc.) may also be considered.
- Postdoctoral training/fellowship in medical/drug information or residency in clinical practice/pharmaceutical industry setting preferred.
Key Responsibilities:
- Provide accurate clinical and technical product knowledge in response to inquiries from healthcare professionals and stakeholders.
- Ensure timely, accurate, and compliant responses to unsolicited medical information requests from HCPs, payers, and healthcare organizations.
- Support and guide the Medical Information Call Center, including escalated cases, staff training, and ongoing coaching.
- Develop and maintain a product knowledge database, including standard response letters (SRLs) and FAQs, ensuring the highest level of scientific accuracy.
- Review and analyze reports and metrics to identify insights, trends, and knowledge gaps.
- Collaborate with internal teams (Clinical Development, Commercial, Market Access, Legal, Regulatory) to ensure accuracy and balance in scientific communication.
- Review new data proactively and update medical information resources accordingly.
- Support the Promotional Material Review Committee (PMRC) and Scientific Review Committee (SRC) to ensure compliant and accurate information.
- Assist with coordinating, escalating, and reviewing legal contracts related to Medical Affairs activities.
- Perform other Medical Information-related functions as needed.
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