Pharmacist

DM Clinical Research; Jersey City (NJ); On-site; USD 80,000 - 100,000; Full time

Job summary

A clinical research organization is seeking a Pharmacist for the Unblinded Clinical Research Coordinator role in Jersey City. The successful candidate will be responsible for dispensing investigational products as part of clinical trials, ensuring compliance with study protocols, and managing medication inventory. Candidates should have a high school diploma, clinical experience, and strong communication skills. Proficiency in computer software such as Word, Excel, and Google Docs is also required. Bilingual candidates are preferred. This position offers the chance to work in a fast-paced and rewarding environment.

Qualifications

• High school diploma or equivalent required.
• Clinical experience preferred.
• LPN or CMA credentials required.

Responsibilities

• Compound and dispense prescribed investigational products.
• Supervise and maintain records of medications.
• Ensure compliance with study-specific blinding plans.
• Provide consultative support about drug preparation and dosing.
• Manage inventory, ensuring expired items are removed.

Skills

Computer proficiency

Excellent communication skills

Customer service skills

Outgoing personality

Attention to detail

Multitasking

Bilingual (Spanish)

Education

High School Diploma or equivalent

Foreign Medical Graduate

Tools

Word

Excel

Outlook

Google Docs

Job description

DM Clinical Research is looking for a Pharmacist to fill our Unblinded Clinical Research Coordinator role and join our team. This individual will be responsible for dispensing Investigational Products (IP) as part of clinical research trials.

Duties & Responsibilities:

• Compound and dispense prescribed IP.
• Supervise and maintain records of all medications.
• Ensure compliance with study‑specific blinding plans.
• Provide consultative support regarding the preparation and dosing of drugs.
• Maintain documentation of IP accountability: receipt, dispensing, return to sponsor/destruction.
• Interpret clinic schedule and protocol into a resource that can be used to identify the date/time to compound/prepare and dispense IP for clinical trials.
• Understand and apply all applicable site procedures.
• Ensure receipt and proper storage of IP and bioretention samples.
• Manage inventory, ensuring that expired items are removed from the inventory prior to expiration, and purchasing, and delivery processes for the pharmacy.
• Review protocols and provide input on clinical and pharmacy supply needs.
• Meet with sponsors, monitors, auditors, and regulatory authorities to review drug accountability and other study‑specific information.
• Temperature reporting.
• Any other duties/tasks assigned by the manager, computer proficiency, especially Word, Excel, Outlook, and Google Docs.

Knowledge & Experience:

Education:

• High School Diploma or equivalent required
• Foreign Medical Graduate is a plus

Experience:

• Clinical Experience

Credentials:

• LPN (Licensed Professional Nurse) or CMA (Certified Medical Assistant)

Knowledge and Skills:

• Computer proficiency, especially Word, Excel, Outlook, and Google Docs.
• Excellent communication and customer service skills.
• Outgoing personality; Well‑organized with attention to detail.
• Must be able to multitask.
• Bilingual (Spanish) preferred but not required