Research Pharmacist - part time

CTI

Plymouth (MI)

Presencial

USD 90 000 - 130 000

Tempo integral

Há 12 dias

Uma candidatura completa num minuto

Currículo e carta de apresentação personalizados, prontos a enviar.

Ultrapassa os filtros ATS

Vantagens oferecidas por esta oferta de emprego

Hybrid work opportunities
Tuition reimbursement
Health benefits
Paid parental leave
Vacations packages

Resumo da oferta

CTI Clinical Trial and Consulting Services is seeking a licensed pharmacist to join our global CRO team. You will review protocols, develop pharmacy procedures, and manage investigational products, ensuring compliance with protocol requirements and regulatory standards.

The ideal candidate holds a BS/MS/PharmD in Pharmacy, active State Board license, and 2+ years of pharmacy practice experience. CTI offers career development, competitive benefits, and a collaborative, high‑quality (hybrid) work

Qualificações

  • Active pharmacy license with the applicable State Board of Pharmacy.
  • Bachelor of Science, Masters, or Doctor of Pharmacy degree.

Responsabilidades

  • Review protocols, pharmacy manuals, and study documents to assess investigational product requirements and feasibility.
  • Develop and implement study-specific pharmacy procedures in accordance with protocol and SOPs.
  • Receive, inspect, store, dispense, and destroy investigational products following regulations.
  • Provide evidence-based drug information to investigators to support patient care.
  • Ensure all pharmacy activities comply with sterile/non-sterile regulations and GCP/ICH/FDA rules.
  • Maintain sterility and environmental controls in the pharmacy area and monitor storage conditions.
  • Maintain inventory, accountability, and documentation throughout the study lifecycle.
  • Assist in development and management of pharmacy policies and SOPs.
  • Prepare for sponsor audits, monitoring visits, and inspections.
  • Collaborate with investigators, sponsors, and site personnel on investigational product activities.

Conhecimentos

Independent work
Electronic documentation systems
Regulatory knowledge
State pharmacy license

Formação académica

Pharmacy degree (BS/MS/PharmD)

Descrição da oferta de emprego

CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the lifecycle of development, from drug concept to commercialization. CTI is headquartered in the Greater Cincinnati, OH region with global operations in collaboration with pharmaceutical, biotechnology, and medical device firms. For more information, visit www.ctifacts.com

What you'll do:
  • Review protocols, pharmacy manuals, and study related documents to assess investigational product requirements and operational feasibility
  • Develop and implement study-specific pharmacy procedures in accordance with protocol requirements and organizational SOP
  • Receive, inspect, document, store, prepare, compound, label, dispense, return, transfer, and destroy investigational products in compliance with protocol requirements and applicable regulations
  • Provide evidence-based drug information to physician investigators to ensure proper management of medical care for subjects
  • Ensure all pharmacy activities are conducted according to applicable sterile and non-sterile compounding regulations
  • Maintain sterility of CTI CRC IDS Pharmacy sterile compounding area in accordance with SOPs, State, and Federal rules and regulations
  • Ensure appropriate environmental controls and storage conditions, including temperature monitoring and documentation for investigational products
  • Ensure pharmacy operations comply with Good Clinical Practice (GCP), International Council for Harmonization (ICH) guidelines, FDA regulations, state pharmacy regulations, and organizational policies
  • Maintain accurate investigational product inventory, accountability, reconciliation, and documentation throughout the study lifecycle
  • Assist in the development and management pharmacy policies and standard operating procedures (SOPs)
  • Maintain drug accountability records and ensure readiness for sponsor audits, monitoring visits, regulatory inspections, and internal quality reviews
  • Collaborate with investigators, research coordinators, sponsors, CRO representatives, and other study personnel regarding investigational product-related activities
  • Request assistance and technical advice from Director, Research Site Operations, Vice President, Research Site Operations, Pharmacist Manager, Principal Investigators and Site Medical Director
  • Behave in a cooperative and constructive manner; follow all company policies, state, local, federal and other applicable laws and guidelines; comply with any and all job-specific requirements
  • Maintain knowledge and expertise across multiple therapeutic areas through clinical and scientific literature review, ongoing awareness of industry practices, and participation in professional activities
  • Perform other duties
What you'll bring:
  • Ability to work independently while collaborating effectively within interdisciplinary teams
  • Proficient in electronic documentation systems
  • Knowledge of State and Federal regulations relating to the storage and dispensing of investigational and marketed drug products
  • Active pharmacy license with the applicable State Board of Pharmacy
  • Bachelor of Science, Masters, or Doctor of Pharmacy degree
  • 2 or more year(s) of experience in a pharmacy practice setting
Why CTI?
  • Advance Your Career – We invest in your professional growth. Through a structured mentoring program, leadership development courses, and access to ongoing education and training opportunities, including tuition reimbursement, you’ll have the tools to achieve your goals. Our dedicated training department supports your successful career at CTI.
  • Be Part of an Award-Winning Team – Join a global team spanning 60 countries, recognized for its award-winning culture that prioritizes people. We support your work-life balance with generous health benefits, vacation packages, hybrid work opportunities, and paid parental leave. Through our CTI Cares program, you’ll have opportunities to give back to your community and the world.
  • Make a Lasting Impact – At CTI, your work directly contributes to advancing medicine. You’ll play a vital role in developing life-changing treatments for patients with chronic and critical illnesses. Together, we move medicine forward, making a difference for those who need it most.

In light of recent increase in hiring scams, if you’re selected to move onto the next phase of our hiring process, a member of our team will reach out to you directly from an@ctifacts.com email address to guide you through our interview process. Please ensure you are applying for jobs directly on our website ( www.ctifacts.com ) or from our verified LinkedIn page.

Please Note
  • We will never communicate with you via Microsoft Teams or text message
  • We will never ask for your bank account information at any point during the recruitment process

Equal Opportunity Employer/Veterans/Disabled

Equal Opportunity Employer This employer is required to notify all applicants of their rights pursuant to federal employment laws.For further information, please review the Know Your Rights notice from the Department of Labor.

Obtém a tua avaliação gratuita e confidencial do currículo.

ou arrasta e larga o ficheiro aqui.

Similar jobs

Ofertas semelhantes que vale a pena comparar

Research Pharmacist - part time
Research Pharmacist - part time

CTI Clinical Trial Services Inc • Plymouth (MI)

Presencial
USD 90 000 - 120 000
Research Pharmacist - part time
Research Pharmacist - part time

CTI Clinical Trial and Consulting Services • Plymouth (MI)

Híbrido
USD 85 000 - 135 000
Hybrid work opportunities
Health benefits
Vacation packages
+1
Regulatory Affairs Study Start Up Specialist (level dependent on experience)
Regulatory Affairs Study Start Up Specialist (level dependent on experience)

CTI Clinical Trial and Consulting Services • Raleigh (NC)

Híbrido
USD 65 000 - 90 000
Health benefits
Vacation packages
Hybrid work from home opportunities
+1
Regulatory Affairs Study Start Up Specialist (level dependent on experience)
Regulatory Affairs Study Start Up Specialist (level dependent on experience)

CTI Clinical Trial and Consulting Services • Covington (KY)

Presencial
USD 60 000 - 90 000
Hybrid work from home
Health benefits
Sr. Clinical Data Manager
Sr. Clinical Data Manager

CTI Clinical Trial and Consulting Services • Covington (KY)

Presencial
USD 85 000 - 125 000
Senior Clinical Project Manager - up to $15K sign-on bonus
Senior Clinical Project Manager - up to $15K sign-on bonus

Consulting, Inc. • Covington (KY)

Teletrabalho
USD 80 000 - 110 000
Career progression support
Generous health benefits
Hybrid work opportunities
Senior Clinical Research Associate (level dependent on experience)
Senior Clinical Research Associate (level dependent on experience)

CTI Clinical Trial and Consulting Services • Covington (KY)

Presencial
USD 70 000 - 95 000
Hybrid work from home
Health benefits
Paid parental leave
+1
Director, Clinical Data Management — Strategic Leader
Director, Clinical Data Management — Strategic Leader

Ctifacts • EUA

Híbrido
USD 140 000 - 190 000
Clinical Project Coordinator
Clinical Project Coordinator

CTI Clinical Trial and Consulting Services • Covington (KY)

Presencial
USD 60 000 - 80 000
Biostatistician II (Clinical Trial Experience Required)
Biostatistician II (Clinical Trial Experience Required)

Ctifacts • Cincinnati (OH)

Teletrabalho
USD 110 000 - 140 000