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Clinical Trials Pharmacist
2 months ago
Mass General Brigham is seeking a highly skilled Clinical Trials Pharmacist to join our team in Everett, Massachusetts.
This is a unique opportunity to work in a dynamic environment where you will be responsible for coordinating, collaborating, and providing expertise in support of drug clinical trials.
Key Responsibilities- Review new protocols and amendments for drug safety and feasibility.
- Review protocol documents and draft dispense instructions.
- Act as a liaison for principal investigators, the research office, sponsors, pharmacy, and the Institutional Review Board (IRB).
- Ensure medication orders comply with approved protocols.
- Dispense research medication to subjects enrolled in clinical trials.
- Review patient medications for appropriateness and potential drug interactions.
- Triage and participate in sponsor monitoring visits and audits.
- Manage investigational drug inventory for studies.
- Oversee the safe handling and preparation of investigational medications.
- Provide drug information to other healthcare professionals.
- Review new drug protocols as IRB ancillary reviewer.
- Promote a culture of safety and adhere to established practices and policies.
- Participate in the training and mentorship of new employees, students, and residents.
- Act as a liaison between CTP and compounding, as well as other areas within the department of pharmacy.
- Assist with special projects assigned by the manager.
- Ensure adequate communication is maintained between staff for continuity of service.
- Participate in and identify quality improvement projects.
- Oversee technician activities and perform quality control checks.
- Attend and participate in Institutional Review Board (IRB) meetings.
- Complete reports, including Safety Reports and Notes to File.
- Comply with state and federal laws pertinent to pharmacy and investigational drug use.
- Massachusetts Pharmacist License in good standing.
- Hospital Pharmacy Experience.
- Research pharmacy experience is preferred.
- Non-sterile and Sterile compounding experience is preferred.
- Human Subject Research Protection (HSRP) certification is preferred.
- Good Clinical Practice (GCP) certification is preferred.
- Excellent verbal and written communication skills.
- Proficient computer-related skills, including Microsoft Office.
- Fluency in English.
- Excellent interpersonal and communication skills.
- Ability to recognize emergency situations and respond appropriately.
- Excellent comprehension of written policies and procedures.
- Ability to make appropriate decisions and develop follow-up actions.
- Attention to detail and organizational ability.
- Ability to work well on a team as well as independently.
- Ability to plan, organize, and prioritize.
- Ability to motivate and develop others.
- General understanding of compounding testing requirements.
- Ability to meet deadlines.
- Competent in math skills, including proportions, ratios, and conversions.
- Excellent telephone skills.
- Ability to monitor and assure security of narcotics and controlled substances in accordance with hospital policy and Federal and State Law.
