Director, Pharmacy Site Operations Job at InnovAge (Boulder)

Director of Pharmacy, Acute Care Clinical Services

The Director of Pharmacy, Acute Care Clinical Services provides clinical leaders...

Location

United States of America , Rochester

Salary:

158350.00 - 237515.00 USD / Year

University of Rochester

Expiration Date

Until further notice

Requirements

Bachelor’s degree in pharmacy required
Master’s degree preferred
5 years of experience in hospital pharmacy or equivalent combination of education and experience required
Post Graduate residency or fellowship training preferred
3 years of experience in pharmacy management required
Licensed Pharmacist in New York State upon hire required

Job Responsibility

Provides clinical leadership for the Department of Pharmacy at Highland Hospitals and Strong, with a focus on developing, implementing, and integrating system level acute care clinical pharmacy services
Uphold standards set by the department, the institution, and regulatory agencies while establishing and leading high-quality clinical services that support optimal patient outcomes
Active participation in system level formulary management and therapeutic program proposals to promote the cost-effective and appropriate use of medications
Providing drug information services and education for pharmacy and patient care staff
Guiding clinical pharmacy services throughout the hospital system, including participation on multidisciplinary committees
Contribute to the development of system-wide clinical pathways, protocols, education, and quality assurance initiatives
Maintain competencies in both clinical practice and leadership to effectively coach, mentor, train, and support staff
Establish partnerships and collaborations with faculty, clinical and administrative leaders throughout the organization to establish programs and processes aimed at delivering cost-effective and safe drug therapy
In collaboration with system leadership, plan, develop, and implement clinical pharmacy services focused on strategic initiatives and system care delivery models
In collaboration with System and site leadership, develop an effective plan to integrate operational and clinical activities of the pharmacy staff to establish efficient and effective strategies to achieve departmental and system objectives

Fulltime

Director, Regional Head Site Management & Oversight, EMEA

The Director, Regional Head Site Management & Oversight provides strategic leade...

Location

Salary:

Not provided

The Muse

Expiration Date

Until further notice

Requirements

Bachelor's degree or equivalent in life science, nursing, pharmacy, medical laboratory technology
12 years+ relevant clinical research experience within the pharmaceutical industry
Experience in leading and managing a professional team with strong experience in site management, monitoring and overseeing large and/or complex global clinical trials
A solid understanding of the drug development process, and specifically, each step within the clinical trial process
Robust budget forecasting and management experience
Thorough knowledge of ICH guidelines/GCP and its applicability to all stages of the clinical development process
Proven experience in overseeing vendors and CROs
Must have experience as a mentor and coach others through peer-to-peer interactions and to develop reporting personnel to grow in complex clinical project management capabilities
Skilled at independently navigating new or novel indications, study/program approaches, and unique challenges
Must have excellent understanding of all tasks involved in a clinical development program(s) from developing a protocol through to finalizing a clinical study report

Job Responsibility

Responsible for operational oversight of the site, site health and monitoring activities
Support QA audit and inspection planning, and implementation of CAPAs as needed
Identify and proactively mitigate site-level risks impacting recruitment, retention, data quality, or compliance, in partnership with CROs
Provide study support on escalated site issues related to study delivery by coordinating communications and resolution efforts
Support sites in understanding study expectations, timelines, and required deliverables
Be accountable for effective site recruitment planning and delivery, consistent with global and/or country plan and local targets in collaboration with CROs
Responsible for enrollment support and ensure progress by responding to recruitment issues from investigators/CROs
Build and maintain strong, trusted relationships with investigators and site staff - Face of CSL
Serve as the sponsor primary point of contacted for assigned studies
Understand site capabilities, constraints, and strategic priorities to improve site engagement and long-term collaboration

What we offer

Health Insurance
Dental Insurance
Vision Insurance
Life Insurance
Short-Term Disability
Long-Term Disability
FSA
HSA
Mental Health Benefits
Adoption Leave

Fulltime

Director, Pharmacovigilance

This is a unique opportunity to join a growing Pharmacovigilance team. This PV e...

Location

United States , Cambridge

Salary:

210000.00 - 260000.00 USD / Year

Beam Therapeutics

Expiration Date

Until further notice

Requirements

Degree in Pharmacy, Nursing, Epidemiology, Biosciences or equivalent degree with pharmaceutical industry background and proven competence in PV
Healthcare professional degree preferred (Nurse Practitioner, Physician Assistant, RN/BSN, Pharm D, MD, or equivalent)
10+ years’ pharmaceutical industry experience, including a minimum of 5 years’ experience in PV
Knowledge of MedDRA dictionary, clinical trial methodology, medical terminology, and general principles of clinical assessment of AEs
Demonstrated knowledge of global PV regulatory environment with working knowledge of international regulations including but not limited to FDA, EU, GVP, ICH guidelines and regulations pertaining to clinical development and post-marketing safety environments
Working knowledge of industry standard safety databases (ARGUS and ARISg) and other electronic data capture systems
Experience reviewing cumulative safety data with ability to interpret, synthesize and communicate complex clinical /pharmaceutical information and safety data
Experience in the preparation and authoring of pre- and post- aggregate safety reports
Thorough understanding of the drug development process and context applicable to safety surveillance activities
Ability to execute and follow-through to completion and documentation

Job Responsibility

Oversight of day-to-day safety monitoring activities and safety operations of clinical trials for assigned product(s)
Provide PV subject matter expertise on clinical development teams and other cross-functional forums throughout the company
Ensure that safety reports for assigned products are triaged, processed and submitted/distributed as required per global requirements and applicable SOPs
Perform individual case safety report assessments for clinical trial safety reports, including review of Analysis of Similar Events, as applicable
Contribute to the development and review of clinical, regulatory, and scientific documents including clinical study protocols, informed consent forms, study plans, clinical study reports, manuscripts/journal articles, scientific abstracts/posters, case report forms, statistical analysis plans, and/or other documents as needed
Facilitate internal cross-functional Safety Management Committee and/or other safety governance/review meetings
including coordinating materials, data outputs and presentation, agenda and minutes
Work closely with the Medical/Safety Lead to support signal detection activities, which may include: preparing signal assessment, tracking, and validation documents
leading cross functional teams to assess safety signals
preparing action and communication plans to mitigate/manage product risks

Fulltime

Pharmacist Consultant - Long Term Care

We’re building a world of health around every individual — shaping a more connec...

Location

United States , Atlanta

Salary:

106200.00 - 168750.00 USD / Year

CVS Health

Expiration Date

June 29, 2026

Requirements

Candidate should reside in Atlanta or surrounding area
Active pharmacist license in good standing in Georgia
Ability to visit customer facilities located in Georgia
3 years of experience in a clinical pharmacy practice
1 year of long term care pharmacy practice as a consultant pharmacist
Additional pharmacist license in states of Tennessee and Alabama
Immunization certified or willingness to become certified
Certification in geriatrics and/or gerontology preferred
Bachelor of Science Degree in Pharmacy or Doctorate of Pharmacy

Job Responsibility

Ensure facilities remain compliant and aligned with federal regulations
Complete clinical reviews as required by federal and state regulation
Own issue resolution and communicate early warning signs of potential issues
Drive adoption of Omnicare programs and service offerings
Use existing customer relationships to promote and drive organic growth as well as new business
Conduct Executive Reviews and other customer meetings as required
Collaborate with Account Management, Sales and Operations to meet overall site goals and objectives
Perform Medication Regimen Reviews (MRR) as outlined by regulation or contract for facility type and provide written reports of these reviews to applicable facility staff
Spend an appropriate amount of time on each resident's review as defined by their clinical needs
Use OSC2OR software on-site to generate MRR, including therapeutic interchange and Omnicare clinical program-related recommendations and document responses to previous recommendations

What we offer

Paid Time Off
Health/Dental/Vision Insurance
401K with a company match
medical, dental, and vision coverage
paid time off
retirement savings options
wellness programs

Fulltime

Senior Director, Quality Assurance GCP

The Senior Director, Quality Assurance GCP is a key role within Hemab's Quality ...

Location

United States , Boston

Salary:

Not provided

Life Science Talent

Expiration Date

Until further notice

Requirements

Advanced degree in life sciences, pharmacy, or a related field
Minimum 10 years of experience in GCP quality assurance within the pharmaceutical or biotechnology industry, with at least 3–5 years in a senior or leadership role
Demonstrated experience planning and conducting GCP audits across a range of audit types (CRO, site, vendor, systems)
Strong knowledge of ICH E6(R2/R3), EU Clinical Trial Regulation (536/2014), FDA GCP regulations, and related guidance documents
Experience working in an outsourced or virtual operating model, with a solid understanding of sponsor oversight responsibilities
Proven ability to manage regulatory inspections and lead inspection readiness programmes
Experience authoring and approving GCP SOPs and quality documentation
Excellent interpersonal and communication skills, with the ability to influence and partner across functions and with external stakeholders
Self-driven, pragmatic, and comfortable operating in a lean, fast-paced environment

Job Responsibility

Audit Planning and Execution
Quality Events Management
Support to Clinical Trial Teams
Inspection Readiness
Quality Working Group Participation
SOP Authorship and Approval
Building a Fit-for-Purpose Quality Organization

Fulltime

Associate Director, Sterility Assurance

The Associate Director, Sterility Assurance, DP Manufacturing is a senior techni...

Location

United States , Norwood

Salary:

142500.00 - 256500.00 USD / Year

Moderna

Expiration Date

Until further notice

Requirements

Bachelor's degree in Microbiology, Life Sciences, Pharmacy, or related field (Master's or Ph.D. preferred)
8+ years in sterility assurance, quality control, sterile pharmaceutical manufacturing, or aseptic processing roles
Deep expertise in isolator-based manufacturing, EM programs, contamination control, media fills, and aseptic filling operations
Strong expertise in risk assessment facilitation
Direct involvement in regulatory inspections, root cause investigations, and Quality System document ownership
Demonstrated aptitude or ability to learn in order to gain a strong understanding of GxP regulations

Job Responsibility

Lead and maintain the Contamination Control Strategy (CCS) for MTC-E, ensuring alignment with EU Annex 1, FDA aseptic guidance, and internal quality expectations
Ensure practical, risk-based integration of the CCS into isolator operations, cleanroom design, gowning practices, material and personnel flow, environmental controls, and aseptic process execution
Provide sterility assurance expertise for site changes, process improvements, and operational decisions that may impact contamination control
Provide expert sterility assurance guidance on the EM program (strategy, zoning, sampling design, alert/action levels, and trending) and partner with QC to ensure effective monitoring and response aligned with contamination control strategy
Lead or support investigations with potential impact to sterility assurance (e.g., EM excursions, media fill failures, decontamination issues, bioburden or sterility failures), ensuring robust root cause analysis and effective corrective and preventive actions
Present EM performance, contamination control risks, and key trends to site leadership and drive data-based decision-making
Own and author sterility assurance-related Quality System documentation, including change controls, risk assessments, CAPAs, deviations, and other records associated with contamination control, EM, or aseptic practices
Ensure records are scientifically sound, timely, and aligned with site and global quality system requirements
Serve as a key leader in inspection and audit readiness activities, including internal audits, client audits, and regulatory inspections
Act as subject matter expert for CCS, EM, aseptic execution, isolator operations, media fills, and related sterility assurance topics

What we offer

Best-in-class healthcare coverage, plus voluntary benefit programs to support your unique needs
A holistic approach to well-being, with access to fitness, mindfulness, and mental health support
Family planning benefits, including fertility, adoption, and surrogacy support
Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
Savings and investment opportunities to help you plan for the future
Location-specific perks and extras
Eligible for an annual discretionary bonus, other incentive compensation, or equity award

Fulltime

Pharmacy Tech Lead

The Pharmacy Technician Lead is a key member of the pharmacy leadership team, as...

Location

United States , Lakewood

Salary:

23.43 - 35.61 USD / Hour

American Nursing Care

Expiration Date

Until further notice

Requirements

High school diploma or GED equivalent
Registered Pharmacy Tech license within the state of Colorado
4 years pharmacy experience in hospital pharmacy required
Excellent verbal and written communication skills required
2 years lead, supervisory, or management experience preferred

Job Responsibility

Assisting the Director of Pharmacy and pharmacy managers in the planning, management, and supervision of all operational activities related to the pharmacy technician staff
Functions in an advanced practice role as a pharmacy specialist within the pharmacy and on interdisciplinary teams
Coordinate all functions related to technician activities that maintain and improve workflow, safety and efficiency to ensure quality distributive processes and services
Responsible for technician training, competency assessment, disciplinary action, regulatory compliance, scheduling, policy/procedures, oversight, and quality improvement activities
May direct and coordinate technicians across multiple sites

What we offer

Medical
prescription drug
dental
vision plans
life insurance
paid time off
tuition reimbursement
retirement plan benefit(s) including, but not limited to, 401(k), 403(b), and other defined benefits offerings

Fulltime

Director, Value Engineering

Lead the execution of Value Transformation programs as a Practice Leader within ...

Location

United States , San Diego

Salary:

162500.00 - 292400.00 USD / Year

BD

Expiration Date

Until further notice

Requirements

Bachelor’s degree required
Master’s preferred (MBA, MHA, MS)
7+ years in healthcare consulting, operational improvement, or transformation delivery
Experience in matrixed consulting environments with cross-functional delivery teams
Expertise in Lean/Six Sigma and change management methodologies
Clinical literacy across Pharmacy or Nursing preferred
Proven success in benefits realization, KPI management, and delivery standardization
Strong executive influence, communication, and stakeholder engagement skills
Travel Requirement: Up to 65%

Job Responsibility

Translate contractual commitments into executable implementation plans with clear KPIs, baselines, data sources, and validation methods
ensure feasibility and readiness across sites
Lead a multidisciplinary team of Value Engineers (Pharmacy, Nursing, BD Excellence, and Process Improvement) to implement outcomes-focused improvements
Stand up and run implementation governance and a lightweight PMO cadence
Apply SME-driven process improvement rigor
Establish standard work and reusable implementation methodologies
Collaborate with C-suite leaders, department heads, and front-line teams
Oversee benefits validation in partnership with Insights/Analytics and Finance
Drive program management discipline
Provide structured feedback to Value Creation

Fulltime

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Director, Pharmacy Site Operations

Job Description

Job Responsibility

Requirements

What we offer

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