Investigational Drug Services (IDS) Pharmacist, On-site

IQVIA

Garland, TXFull-time

Behavioral Health Market Context

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Benefits

The potential base pay range for this role, when annualized, is $57,700.00 - $209,800.00The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time)Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits

Qualifications

  • Current Pharmacy License in Texas or Virginia (required)
  • Strong knowledge of GCP, GMP, USP <797> and <800>, and clinical trial regulations
  • Ability to lift up to 40 lbs and perform duties requiring manual dexterity and extended periods of sitting/standing

Responsibilities

  • The IDS Pharmacist plays a critical role in ensuring protocol integrity, patient safety, and regulatory compliance throughout the conduct of clinical trials
  • Protocol Compliance: Review protocols, amendments, and study-specific documentation; attend site initiation visits; ensure accurate medication screening and documentation
  • Medication Dispensing & Preparation: Verify dosing accuracy, oversee compounding of investigational products (IP), and ensure compliance with USP <797> and <800>
  • IP Management & Accountability: Maintain inventory, manage drug receipt and returns, ensure proper documentation in Vestigo, and support monitoring visits
  • Administrative & Supervisory Duties: Supervise IDS technicians, maintain SOP compliance, support audits, and contribute to staff training and performance evaluations
  • Education & Training: Orient new staff and maintain required certifications and licenses
  • Data & Document Management: Upload and manage protocol documentation and staff credentials in eDOCs and Vestigo
  • This role offers the opportunity to work closely with leading investigators and contribute meaningfully to clinical trials in a supportive and collaborative environment
  • 5 more items(s)


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