Clinical Trial Site Pharmacist: Impactful Research Role

Bethany-Medical; High Point (NC); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Competitive Yearly Compensation

Medical/Dental/Vision

Generous PTO

Company Paid Holidays

Company-matched 401K Plan

Job summary

Bethany Medical is seeking a Clinical Trial Site Pharmacist to support investigational drug management in High Point, NC. You will ensure proper storage, handling, dispensing, and documentation for clinical trials in collaboration with investigators, coordinators, and sponsors.

The role emphasizes GCP and FDA compliance, meticulous record-keeping, and clear communication with study teams and monitors. This site offers competitive compensation and comprehensive benefits within standard business

Qualifications

• Licensed Pharmacist in good standing.
• Experience in clinical, hospital, or outpatient pharmacy settings.
• Strong knowledge of medication management, safety practices, and regulatory compliance.
• Experience with investigational drug services or clinical trials preferred but not required.
• Strong attention to detail and documentation accuracy.
• Ability to collaborate with investigators, sponsors, and multidisciplinary teams.
• Excellent organizational, communication, and problem-solving skills.

Responsibilities

• Manage investigational drug products per study protocols and regulatory standards.
• Maintain accountability logs, dispensing records, and pharmacy documentation.
• Ensure proper storage, temperature monitoring, and security of investigational products.
• Prepare and dispense investigational medications per protocol and orders.
• Verify dosing requirements and preparation instructions.
• Provide medication-related consultation to investigators and study staff.

Skills

Licensed Pharmacist

Clinical Trials

Regulatory Compliance

Documentation

Team Collaboration

Communication Skills

Job description

Bethany Medical is seeking a Clinical Trial Site Pharmacist to support investigational drug management in High Point, NC. You will ensure proper storage, handling, dispensing, and documentation for clinical trials in collaboration with investigators, coordinators, and sponsors.

The role emphasizes GCP and FDA compliance, meticulous record-keeping, and clear communication with study teams and monitors. This site offers competitive compensation and comprehensive benefits within standard business