Clinical Research Pharmacist: Trial Pharmacy Leader

ADP, Inc.; Webster (TX); On-site; USD 104,000 - 135,000; Full time

Job summary

Tranquil Clinical and Research Consulting Services LLC in Webster, TX is seeking a Clinical Research Pharmacist to manage investigational drugs and trial pharmacy activities. You will work with investigators, sponsors, and CROs to ensure protocol compliance and patient safety throughout the trial lifecycle.

The role covers IP receipt/storage, preparation/dispensing, drug accountability, monitoring visits, and study closeout under applicable regulations and GMP/GCP standards.

Qualifications

• PharmD or equivalent required and active pharmacist license.
• Experience with clinical research or trial pharmacy operations preferred.
• Strong knowledge of GCP and regulatory requirements.
• Detail-oriented with excellent documentation.
• Clear written and verbal communication; team collaboration essential.

Responsibilities

• Oversee trial pharmacy operations including receipt, storage, preparation, dispensing and accountability of investigational products.
• Ensure compliance with FDA, GCP, SOPs, and study protocols.
• Support site initiation, monitoring, and closeout activities; participate in audits.
• Provide education to research staff on investigational drugs and workflows.
• Maintain SIAs, records, and documentation; manage deviations and issues.
• Coordinate with investigators, CROs, and Sponsors to ensure protocol adherence.

Skills

Pharmacist license

Clinical research familiarity

GCP knowledge

Attention to detail

Communication skills

Team collaboration

Pharmacy degree

Education

Doctor of Pharmacy (PharmD) or equivalent

Tools

Electronic trial management systems

Pharmacy information systems

Electronic Health Records

Job description

Tranquil Clinical and Research Consulting Services LLC in Webster, TX is seeking a Clinical Research Pharmacist to manage investigational drugs and trial pharmacy activities. You will work with investigators, sponsors, and CROs to ensure protocol compliance and patient safety throughout the trial lifecycle.

The role covers IP receipt/storage, preparation/dispensing, drug accountability, monitoring visits, and study closeout under applicable regulations and GMP/GCP standards.