Oncology Research Informatics Pharmacist (Sign-On Bonus)

Beth Israel Lahey Health, Inc.

Boston, Northern (MA, KY)

Hybrid

USD 124,000 - 167,000

Full time

14 days+
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Benefits offered by this job

Sign-on bonus

Job summary

Beth Israel Deaconess Medical Center in Boston, MA is seeking a Research Informatics Pharmacist specializing in oncology to support investigational therapies within Epic. You will design, build, and maintain investigational medication records in Willow and treatment plans in Beacon, ensuring accuracy and regulatory compliance.

Collaborating with investigators, research nurses, and clinical trials staff, you will supervise adult research chemotherapy treatment plans, review protocols, and

Qualifications

  • Bachelor's degree in Pharmacy required.
  • Doctorate of Pharmacy (PharmD) preferred.
  • Licensed Registered Pharmacist in Massachusetts required.
  • 3–5 years related work experience.
  • Experience with Epic in an informatics and/or patient care setting.

Responsibilities

  • Designs, builds, and maintains investigational medication records in Willow and treatment plans in Beacon.
  • Reviews protocols and ensures study conduct complies with applicable regulations.
  • Coordinates QA, data analysis, and protocol amendments for investigational plans.
  • Collaborates with multidisciplinary teams to implement quality improvements in clinical trials.
  • Provides training and education to staff on new adult research chemotherapy treatment plans.

Skills

Epic Informatics
Data analysis
Jira
Confluence
SharePoint
MS Office
Communication

Education

Bachelor's degree in Pharmacy
Doctorate of Pharmacy (PharmD) preferred

Tools

Willow
Beacon
Epic
Jira
Confluence
SharePoint

Job description

Beth Israel Deaconess Medical Center in Boston, MA is seeking a Research Informatics Pharmacist specializing in oncology to support investigational therapies within Epic. You will design, build, and maintain investigational medication records in Willow and treatment plans in Beacon, ensuring accuracy and regulatory compliance.

Collaborating with investigators, research nurses, and clinical trials staff, you will supervise adult research chemotherapy treatment plans, review protocols, and

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