Clinical Research Pharmacist II - Dallas, TX

Fortrea • Dallas, TX

18d • Onsite

About The Position

As one of the largest Clinical Research Organizations in the world, we have four Early Phase Clinical Research Units in the UK and US. We are seeking a Clinical Research Pharmacist II who will play a critical role in supporting clinical trials by ensuring the safe and compliant preparation and dispensing of investigational compounds. This position offers the opportunity to collaborate with sponsors, regulatory bodies, and internal teams while driving process improvements and maintaining the highest standards in pharmaceutical research. This is a full-time, office-based position in Dallas, TX. If you join us, you will work with some of the world´s leading pharmaceutical, biotechnology, and medical device companies in a vital stage of clinical development: establishing the safety, tolerability, and pharmacokinetics of a new drug. Many are drawn to their profession because of its direct impact on patient care. If this is your case, you will not miss that working in Phase 1 trials. Whilst allowing you to practice your clinical skills and knowledge, you´ll be involved with the latest medical technologies and treatments, witnessing their development firsthand. When the drug you work with gets approved, you know you´ll touch many patient´s lives around the world.

Requirements

• Registered Pharmacist or PharmD in applicable state.
• Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
• 5+ years of pharmacy experience.
• 2+ years in clinical research.
• Strong knowledge of GxP standards (GMP, GCP) and regulatory requirements.
• Proficiency in Microsoft Office Suite.
• Strong written and verbal communication skills.

Nice To Haves

• Hospital setting preferred.

Responsibilities

• Serve as a subject matter expert on pharmaceutical aspects of clinical trials.
• Oversee all phases of pharmacy-related study conduct with minimal oversight.
• Develop and maintain SOPs, pharmacy manuals, and compliance processes.
• Liaise with sponsors and regulatory agencies to ensure adherence to GxP standards.
• Support feasibility reviews, cost analysis, and sourcing of pharmacy materials.
• Maintain pharmacy facilities, equipment, and safe working practices.
• Provide technical guidance to clinical teams and assist with training programs.
• All other duties as needed or assigned.

Benefits

• Regular, full-time, or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including but not limited to:
• Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers)
• 401(K)
• Paid time off (PTO)
• Employee recognition awards
• Multiple ERG’s (employee resource groups)

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Ph.D. or professional degree
• Number of Employees: 5,001-10,000 employees