Investigational Pharmacist

Pharmacy

If you are a current Duly/SBC/QMG employee, please apply through the Internal Career Site.

At Duly Health and Care, you are supported to do your best work and make a meaningful impact every day. You will be part of a collaborative, physician-led team that works as one and puts patients at the center of everything we do.

With a connected network of providers, care teams, and services across primary and specialty care, surgery centers, imaging, lab, and therapy, you are part of a system designed to deliver high-quality, coordinated care. Together, we create an environment where you can grow, contribute, and help improve the experience and outcomes for every patient we serve.

Benefits:

• Comprehensive medical, dental, and vision benefits that include healthcare navigation assistance.
• Access to a mental health benefit at no cost.
• Employer provided life and disability insurance.
• $5,250 Tuition Reimbursement per year.
• Immediate 401(k) match.
• 40 hours paid volunteer time off.
• A culture committed to community engagement and social impact.
• Up to 12 weeks parental leave at 100% pay and a financial benefit for adoption and surrogacy for non-physician team members once eligibility requirements are met.

Position Highlights:

Full-Time

Monday-Friday 8:30am-5pm

Lisle

We are seeking a highly motivated and detail-oriented Investigational Pharmacist to join our multidisciplinary team within a busy multispecialty clinic. This role will support and manage investigational drug studies, including Phase I-IV clinical trials. The ideal candidate will bring a strong background in pharmacy practice along with a passion for clinical research, regulatory compliance, and patient-centered care.

• Investigational Drug Management:

• Receive, store, prepare, dispense, and dispose of investigational drugs according to protocol, regulatory, and sponsor requirements.

• Maintain accurate drug accountability records and manage inventory.

• Ensure investigational products are handled in accordance with Good Clinical Practice (GCP), Good Manufacturing Practice (GMP), and FDA regulations.

• Clinical Trial Support:

• Collaborate with clinical investigators, research coordinators, and sponsors to ensure timely trial execution.

• Assist in study startup activities including protocol review, feasibility assessments, and site preparation.

• Participate in initiation, monitoring, and close-out visits from sponsors or CROs.

• Develop and maintain ERXs, therapy plans, and treatment plans for the investigational drugs and study treatment regimen.

• Patient Safety and Education:

• Educate clinic staff on study medications, protocols, dosing schedules, and potential adverse effects.

• Compliance & Documentation:

• Ensure all pharmacy-related research activities comply with protocols, FDA regulations, ICH guidelines, and institutional policies.

• Maintain thorough and accurate documentation of all investigational drug activities.

• Cross-functional Collaboration:

• Act as a liaison between the research organization, clinic departments, and external sponsors/CROs.

• Participate in multidisciplinary team meetings to discuss study progress, challenges, and solutions.

• Collaborate with the Research department to enable timely and accurate invoicing for investigational pharmacy services.

• Training & Development:

• Provide training to pharmacy staff and clinical personnel involved in research activities.

• Stay updated on industry best practices, new regulations, and therapeutic developments.

EXPERIENCE

• Education:

• Doctor of Pharmacy (PharmD) or equivalent from an accredited school of pharmacy.

• Licensure:

• Active and unrestricted pharmacist license in Illinois.

• Experience:

• Minimum of 2 years of clinical pharmacy experience, preferably in a research or hospital setting.

• Prior experience in clinical trials or investigational drug services is highly desirable.

• Skills:

• Excellent organizational, communication, and documentation skills.

• Proficiency in pharmacy information systems and clinical trial management systems is a plus.

• Epic

Qualifications:

• Board Certification (e.g., BCOP, BCPS, etc.)
• Certification in Clinical Research (e.g., ACRP or SOCRA)
• Familiarity with multispecialty practice environments and complex therapeutic areas (e.g., oncology, neurology, cardiology)

The compensation for this role includes a base pay range of $107,855-161,784, with the actual pay determined by factors such as skills, experience, education, certifications, geographic location, and internal equity. Additional compensation may be available through shift differentials, bonuses, and other incentives. Base pay is only a portion of the total rewards package.

Artificial Intelligence Disclosure

Artificial Intelligence (AI) tools may be used in some portions of the candidate review process for this position, however, all employment decisions will be made by a person.