H-1B Visa Pharmacy Manager Jobs

Job Summary

The IDS Pharmacy Manager must be knowledgeable in standard pharmacy practices, including USP<797> and USP<800>, in addition to research and oncology care practices. The IDS Pharmacy Manager advocates for patient safety and protocol integrity, adheres to patient care standards, and communicates effectively to ensure effective conduct of clinical trials and quality patient care. The IDS Pharmacy Manager is responsible for evaluating, hiring, and training new staff.

Essential Duties and Responsibilities

Essential and other important responsibilities and duties may include but are not limited to the following:

Protocol Compliance:

• Reviews potential future protocols for feasibility and attends weekly protocol review meetings.
• Attends site initiation visits.
• Participates in quality control checks for study-specific forms, both for new studies and for protocol updates.
• Creates IDS specific training documents for staff for new protocols using the IDS template.
• Reviews all investigational protocols, amendments, and clarification letters. Updates concomitant medication screening note, medication diary/diaries and/or other study-specific forms, Varian Regimens, and Vestigo (electronic drug accountability program) as required.
• Creates IDS specific training documents for staff as required for protocol updates/IP manual updates, etc.
• Participates in providing timely, informative, and accurate communication with the interdisciplinary team to ensure protocol compliance and timeliness of protocol-related procedures.
• Performs concomitant medication screens on all patients who are undergoing screening for clinical trial enrollment. Answers concomitant medication questions for research staff and patients throughout trial enrollment.
• Ensures evidence-based symptom management is provided to patients as permitted by the protocol.

Medication Dispensing and Preparation for Conventional and Investigational Products (IP):

• Reviews all orders for accuracy of dose and dose calculations.
• Reviews patient-specific factors to determine eligibility for treatment, including, but not limited to laboratory values, required protocol assessments (ECHO/MUGA, disease assessments, ophthalmology exam, pulmonary function, etc.), consent/reconsent and toxicity resolution.
• Develops compounding tools for all IV investigational agents and trains technicians on mixing process for all IP and conventional agents, if required.
• Checks all IV and PO doses prepared by the IDS Pharmacy technician.
• Have an excellent working knowledge of good clinical practice (GCP), good manufacturing practice (GMP) and all procedures, legislation or national guidelines relating to aseptic preparation (USP<797>) and dispensing of hazardous medication (USP<800>) and clinical trials.
• Assist in the provision of a high-quality investigational drug service, including provision of pharmaceutical care.
• Ensure that IDS services are flexible and responsive to research staff and that the services meet patient requirements/needs.
• Provides drug information to physicians, nurses, and other health care professionals.

Management of Investigational Product and Drug Accountability:

• Maintains responsibility for the management of the inventory for protocols, including ordering, receiving, and returning IP, as required.
• Ensure that correct procedures for receipt of IP and storage of IP are followed.
• Maintain appropriate and accurate records for all protocols, including drug accountability, drug receipt, temperature monitoring, expiration/retest dating and staff training, etc.
• Ensure that procedures for the return and disposal of IP are current and being followed.
• For oral IP: review patient medication diaries and IP returns for accuracy and completeness in conjunction with the treatment room nurses and research coordinators. Document this review and return it in Vestigo. Ensure medication diary is scanned and uploaded into eDOCs.
• Monitors IDS activities, daily, to ensure adherence to protocols, standard operating procedures, IDS Workflows and dispensing procedures.
• Ensure that products used in clinical trials are managed according to standard operating procedures (SOPs), Good Clinical Practice (GCP), Good Manufacturing Practice (GMP) and any other applicable regulations.
• Assist with monitoring visits and answering any monitor queries.

Administrative and Supervisory Responsibilities:

• Provides direct supervision and training to IDS pharmacists.
• Provides direct supervision and training to IDS pharmacy technicians for preparation of medications for dispensing, including compounding of IV and hazardous medications and oral IP doses.
• Complies with NEXT Oncology SOPs and Workflows ensures all IDS staff are appropriately trained and in compliance with SOPs.
• Contributes to the development, integration and monitoring of written procedures and workflows covering all aspects of the IDS.
• Oversees monthly conventional inventory, investigates inventory discrepancies/issues, and performs adjustments, as required.
• Provides technical and procedural guidance.
• Monitors IDS activities, daily, to ensure adherence to proper inventory record maintenance.
• Provides coverage for other IDS employees when they are out due to illness or scheduled PTO, including compounding duties.
• Collects and documents workload measurement statistics, provides other data, as required.
• Supervises and provides direction to all IDS staff.
• Contributes to the development of corrective and preventive action plans for unanticipated problems, deviations, violations, and issues of noncompliance.
• Performs annual review for both IDS pharmacists and provides input to performance appraisals of IDS pharmacy technicians.
• Assists the VP of Investigational Drug Services in preparation and review of documentation for audits.

Education Responsibilities:

• Orients IDS staff, pharmacy residents and pharmacy students to the IDS role with respect to protocols, as required.
• Maintain continuing education requirements to maintain Pharmacy and Preceptor License, any certifications and protocol compliance training, i.e. GCP/PHRS.
• Maintains sterile compounding and hazardous compounding certification.

Data and Document Management and Information Technology:

• Assist in the scanning, review and uploading of protocol documentation into eDOCs.
• Upload resume, license(s), certification(s) and training documents for IDS employees into eDOCs.
• Vestigo will be utilized as our IP and protocol management software. All IDS staff will become knowledgeable in the use of this program.

Required Education and Experience:

• Current Pharmacy License (required) in the state the NEXT Oncology position is located.
• Current Pharmacy Preceptor License (preferred) in the state the NEXT Oncology position is located.
• Current IV Certification (required)
• Current Chemotherapy Certification (required)

Why Join Us?

At NEXT Oncology (an Avacare Business), you’ll be part of a mission-driven team that values collaboration, precision, and patient safety. Our team is known for its supportive culture, strong communication, and commitment to excellence in clinical research.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law.

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Compensation

The potential base pay range for this role, when annualized, is $88,200.00 - $220,300.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

LOCATION

Houston, United States of America

Job Type

Full time

Work Arrangement

Office-based

You’ll work primarily from one of our office locations, collaborating closely with colleagues in a dynamic, team-oriented environment. This setting offers access to on-site resources, real-time interaction and opportunities to build strong relationships through in-person work.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.