Pharmacist

DM Clinical Research; New York (NY); On-site; USD 70,000 - 90,000; Full time

Job summary

A clinical research organization is seeking a Pharmacist for the position of Unblinded Clinical Research Coordinator in New Jersey. This role involves dispensing Investigational Products and ensuring compliance with clinical trial regulations. The ideal candidate should have a High School Diploma and relevant clinical experience. Proficiency in Microsoft Office and excellent communication skills are essential, with bilingual (Spanish) skills preferred. Join our team to support crucial research efforts.

Qualifications

• Candidate must possess a High School Diploma or equivalent.
• Previous clinical experience is required.
• Credentials as an LPN or CMA are needed.

Responsibilities

• Dispense and compound Investigational Products.
• Supervise medication records and ensure compliance.
• Maintain proper documentation and inventory management.
• Provide consultative support for drug preparation and dosing.
• Meet with sponsors and regulatory authorities regarding accountability.

Skills

Computer proficiency (Word, Excel, Outlook, Google Docs)

Excellent communication skills

Customer service skills

Outgoing personality

Multitasking ability

Bilingual (Spanish) preferred

Education

High School Diploma or equivalent

Foreign Medical Graduate

Job description

DM Clinical Research is looking for a Pharmacist to fill our Unblinded Clinical Research Coordinator role and join our team in New Jersey. 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.

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.