Pharmacist

Integrated Resources INC

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New Haven, CT, us on site Until 8/21/2026 H-1B sponsor history First posted February 23, 2026 Last posted February 23, 2026
Job description

A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Location: New Haven, CT

Duration: 1 year+

The Pharmacist provides operational pharmacy support, under the direction of the Head of Pharmacy, at a clinical development stage biopharmaceutical company. The Pharmacist will also support preparation of investigational doses for volunteers, meeting regulatory requirements for preparation of dose formulations under Good Clinical Practices (GCP) and in accordance with current pharmacy compounding best practices, including but not limited to, USP <797>, <795>, where applicable.

RESPONSIBILITIES: 

• Reviewing and/or executing extemporaneous dispensing records, dosage and administration Instructions, core protocol elements, protocol, informed consent documents, Clinical Supplies Request

• Drafting pharmacy budget for each study

• Completing daily setup work in support of dose preparation activities• Entering randomization data into electronic data capture management system

• Performing dummy run work to support verification of dose preparation

• Quality assurance role on dose preparations

• Pharmacy lead assignment on protocols

• Performing study closeout activities

• Maintaining accurate investigational drug inventories and supplies according to established policies and procedures

• Maintaining accurate control, accountability and distribution of controlled substances

• Dispensing investigational drugs to support clinical investigations

• Blinding of drug supplies

• Compounding and dispensing of oral, topical and parenteral dosage forms and matching placebo formulations

• Maintaining clinical supplies and compounding equipment

• Processing equipment/building repair requests


QUALIFICATIONS AND SKILLS NEEDED:

• Qualifications needed are PharmD degree, CT State licensed pharmacist, at least 3 years of pharmacy practice experience in a setting preparing both sterile and non-sterile dosage forms, and completion of an accredited post-PharmD residency and/or fellowship. Math required.

• Expertise in IV admixture per USP <797> required. 

• The successful candidate is expected to be competent in investigational drug management including protocol support activities; product development and formulation; investigational drug information development; and, control, storage, use, handling and accountability of investigational agents including controlled substances. 

• Must be detail-oriented and possess strong organizational skills and the ability to prioritize multiple tasks/projects.


Feel free to forward my email to your friends/colleagues who might be available.............!!!


Thank You. :)



call me at 732-429-1636 if you are interested and available...!!!!

About this role

Summary

Support clinical development with pharmacy operations, dose preparation, and investigational drug management.

Job title

Pharmacist

Experience level

3+ years

Industry

healthcare

Location requirements

On-site in New Haven, CT, no remote work allowed.

Salary

Not specified

Visa sponsorship

H-1B sponsor history

Management role

No

Skills & keywords

Required skills

PharmDCT licensed pharmacistpharmacy practiceUSP <797>investigational drug management

Preferred skills

residencyfellowshipIV admixtureprotocol support

Specializations

sterile dosage formsnon-sterile dosage formsinvestigational drugscompoundingdrug management
Locations

Structured locations inferred from the posting.

New Haven, CT, USA

On-site City