Dr. Moise Khayrallah Center for Pharmaceutical and Medical Research (PMRC) is currently looking for a Research Pharmacist reporting to the Principal Investigator. This is a central position that is based on the Byblos campus.
Role Summary
The Research Pharmacist is mainly responsible for the oversight, storage, and dispensing of all investigation drug products during a study, ensuring compliance with GCP and other regulatory requirements. S/he plays a critical role in ensuring the safety, efficacy, and data integrity of bioequivalence studies, which are essential for demonstrating that generic drugs provide the same therapeutic benefits as brand-name counterparts.
Main Duties & Responsibilities
- Oversees, stores, and controls all investigational medicinal products (IMPs) used in the study
- Ensures proper storage conditions and temperature monitoring for test and reference drugs
- Maintains inventory control and accountability records for all study medications
- Ensures accurate dispensing of investigational drugs to study participants following specific protocols
- Ensures proper labeling of immediate packaging according to clinical trial requirements
- Ensures appropriate labeling of storage areas and dispensed drug products
- Maintains complete records of investigational product receipt, storage, dispensing, and return
- Creates and maintains audit trails and logs for all medication-related activities
- Documents drug information sections accurately to ensure proper preparation and administration
- Ensures safe handling and preparation of investigation agents
- Verifies FDA approval and local IRB compliance before dispensing
- Protects participant rights, safety, and well-being through proper medication management
- Ensures proper packaging and shipping methods to maintain drug integrity and quality
- Maintains the quality of drug products throughout the supply chain
- Follows Good Clinical Practice (GCP) guidelines for clinical trial conduct
- Adheres to state and federal regulations for dispensing investigational drugs
- Ensures compliance with regulatory standards from bodies like FDA and EMA
- Acts as backup support for unit staff as needed
- Performs other duties pertinent to this job as assigned by the direct supervisor
Minimum Required Qualifications
- * B.S. in Pharmacy with 3 years of experience OR a PharmD with 1 year of experience with a strong background in pharmacokinetics, pharmaceutical sciences, and clinical bioequivalence studies
- Hands-on experience with Investigational Product storage, dispensing, drug accountability, and blinding/randomization under GCP
- Proficiency in Microsoft Office (Word, Excel, Outlook, and PowerPoint)
- Excellent communication skills, both verbal and written, with a professional and empathetic attitude
- Detail oriented and meticulous in all aspects of work
- Positive attitude and strong interpersonal skills; ability to work well independently as well as in team environment
- Strong organizational and multitasking abilities, with the capacity to prioritize tasks and manage time effectively
- Ability to handle sensitive and confidential information with professionalism and discretion
- Good judgment and decision making, active listening, etc
Work Schedule
The standard work schedule for this position is Monday through Friday. Due to the nature of operations and ongoing studies, flexibility is required, including occasional work outside regular hours, on weekends, or on holidays, as necessary to support study activities and maintain business operations.
Interested candidates should email their CVs with a letter of interest outlining the applicant’s relevant experience to [email protected], specifying the job title in the subject line.
CVs should include the exact month and year while listing the candidate’s professional experience and educational background.Closing date for accepting applications is Thursday, November 26, 2026.
No applications will be accepted after this date, and only shortlisted candidates will be notified.
Candidates must have attained the age of majority and satisfy all legal requirements to lawfully reside and work in Lebanon, in accordance with the applicable laws and regulations of the Republic of Lebanon.
The Lebanese American University is an Equal Opportunity Employer.
