Clinical Pharmacist – Research & Compliance

The University of Texas Southwestern Medical Center; Dallas (TX); Híbrido; USD 120.000 - 150.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Healthcare benefits

Paid time off

Retirement programs

Tuition reimbursement

Parental leave

Descripción de la vacante

UT Southwestern Medical Center is seeking a pharmacist to initiate, monitor, and audit investigational drug studies approved by the IRB, ensuring compliance with federal, state, FDA and other regulations. The role serves as a liaison for principal investigators, sponsors, the IRB, and pharmacy, maintaining accurate records and pharmacotherapy documentation.

The position emphasizes collaboration with clinical teams, patient safety, and cost-effective medication management within a

Formación

• Education: BS or PharmD degree;
• 1 year pharmacy experience;
• Eligible for licensure by Texas State Board of Pharmacy;
• Texas license within 30 days of hire;
• ACPE-IV sterile compounding certification upon hire;
• BLS certification upon hire;
• ACLS certification within 180 days for inpatient positions.

Responsabilidades

• Performs duties per policies, procedures, and regulatory standards.
• Manages medication orders, reviews profiles, and considers charges.
• Evaluates drug therapies for safety and efficacy; documents interventions.
• Provides supervision of technicians and validates medications for distribution.
• Audits controlled substances in compliance with laws and policies.
• Contributes to clinical programs and ongoing staff training.
• Supports P&T initiatives and clinical monitoring within pharmacotherapy.

Conocimientos

English proficiency

Educación

BS or PharmD degree

Texas pharmacist license eligible; license within 30 days

ACPE-IV Sterile Compounding certification

BLS certification

ACLS (Advanced Cardiac Life Support) within 180 days

Descripción del empleo

UT Southwestern Medical Center is seeking a pharmacist to initiate, monitor, and audit investigational drug studies approved by the IRB, ensuring compliance with federal, state, FDA and other regulations. The role serves as a liaison for principal investigators, sponsors, the IRB, and pharmacy, maintaining accurate records and pharmacotherapy documentation.

The position emphasizes collaboration with clinical teams, patient safety, and cost-effective medication management within a