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Hearst

Clinical Pharmacist

1w

Hearst

Indianapolis, US · Full-time · $100,000 – $120,000

About this role

Join the healthcare information technology team that's turning drug and medical device data into knowledge used by thousands of hospitals, the majority of U.S. health plans, retail pharmacies, and pharmacy benefit managers. Partnering with information system developers and healthcare institutions, you'll help evolve leading-edge thinking into reality and make a measurable difference in improving human health.

As a Clinical Pharmacist, you will work independently under broad supervision to research source pharmaceutical information, make detailed observations, analyze clinical evidence, and interpret results for possible inclusion within MedKnowledge base content. You will direct and perform data entry tasks, verify team members' data entry, and independently plan and prioritize your work to meet product maintenance standards.

This role is based in Carmel, IN, following a hybrid work model with an expectation to work onsite at least three days per week. You will review daily data change reports, manage internal post-production data audit reports, and bring challenging or controversial clinical issues to the team for discussion.

You will have the opportunity to contribute to process and quality improvement efforts, provide in-services and presentations to group members, and begin fielding customer questions using basic data analytic skills. This position offers a chance to play an essential role in a successful company's continued growth while working with a team that is intelligent, productive, committed, and passionate about making a difference.

Requirements

  • Ability to work independently under broad supervision of a team lead, supervisor, or manager.
  • Experience researching source pharmaceutical information and analyzing clinical evidence.
  • Proficiency in performing and verifying data entry tasks with attention to detail.
  • Ability to independently plan and prioritize work assignments to meet deadlines.
  • Skill in reviewing data change reports and resolving inconsistencies.
  • Basic data analytic skills to identify issues and deliver possible solutions for customer questions.
  • Willingness to bring challenging or controversial clinical issues to the team for discussion.
  • Commitment to contributing to process and quality improvement efforts.

Responsibilities

  • Research source pharmaceutical information, make detailed observations, analyze clinical evidence, and interpret results for possible inclusion within MedKnowledge base content consistent with stated Editorial/DSG policies.
  • Direct and perform data entry tasks and verify data entry performed by other team members.
  • Independently plan and prioritize order of completion for work assigned, ensuring work meets or exceeds stated product maintenance standards.
  • Review timely drug information inheritance through knowledge base drug group rules using daily Apollo reports.
  • Manage and respond to internal post-production data audit reports.
  • Review daily data change reports and take action to resolve any inconsistencies.
  • Develop an understanding of the risks and advantages of key Apollo system forms.
  • Actively contribute to process and quality improvement efforts and provide in-services and presentations to group members.

Benefits

  • Hybrid work model with onsite expectation at least three days per week in Carmel, IN.
  • Opportunity to work with a team that is turning drug and medical device data into knowledge used by thousands of hospitals and healthcare organizations.
  • Role in a successful company with continued growth and a focus on making a measurable difference in improving human health.
  • Chance to provide in-services and presentations and contribute to process improvement efforts.