CrawlJobs Logo

Pharmacy Infectious Diseases Clinical Specialist

baptisthealth.net Logo

Baptist Health

Location Icon

Location:
United States , Boca Raton

Category Icon
Category:

Job Type Icon

Contract Type:
Employment contract

Salary Icon

Salary:

118907.47 - 154579.71 USD / Year

Job Description:

The Pharmacy Clinical Specialist I is expected to take responsibility for establishing and expanding clinical services in area of practice. The development of medication protocols, order sets, and facilitation of medication utilization reviews and performance improvement projects to optimize drug therapy is required. Provides mentorship and is a clinical resource for staff and other health care providers in area of expertise. Provides expertise for clinical activities relating to various programs for the department of pharmacy in order to ensure optimal patient outcomes. Provides drug distributive functions as assigned. Demonstrates ability to work with the patients growth and development based upon population groups, and meet standards of quality as measured by the quality improvement process.

Job Responsibility:

  • Establishing and expanding clinical services in area of practice
  • Development of medication protocols, order sets, and facilitation of medication utilization reviews and performance improvement projects to optimize drug therapy
  • Provides mentorship and is a clinical resource for staff and other health care providers in area of expertise
  • Provides expertise for clinical activities relating to various programs for the department of pharmacy to ensure optimal patient outcomes
  • Provides drug distributive functions as assigned

Requirements:

  • Doctorate
  • Registered Pharmacist
  • Doctorate of Pharmacy (Pharm.D.)
  • If no residency training must have 5 years of practice experience in area of specialty required and Board Certification
  • If no Board Certification must have BPS within one year of hire date
  • PGY1 residency with 2 years practice experience in area of specialty and BPS required
  • PGY2 residency must have BPS within 1 year of hire
  • 5 Years of practice experience in area of specialty required and Board Certification
What we offer:
  • Career growth and development opportunities
  • Comprehensive health and wellness resources
  • Wellness program that can help eliminate medical plan deductible
  • Tuition reimbursement

Additional Information:

Job Posted:
May 15, 2026

Employment Type:
Fulltime
Work Type:
On-site work
Job Link Share:

Looking for more opportunities? Search for other job offers that match your skills and interests.

Briefcase Icon

Similar Jobs for Pharmacy Infectious Diseases Clinical Specialist

Pharmacist 2, Clinical Specialist - Infectious Diseases

As a community, the University of Rochester is defined by a deep commitment to M...
Location
Location
United States of America , Rochester
Salary
Salary:
126258.00 - 163610.00 USD / Year
urmc.rochester.edu Logo
University of Rochester
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Doctor of Pharmacy degree required
  • New York State Pharmacy License upon hire required
  • Board certification in the most relevant specialty area within 2 years required
  • Specialty residence training preferred
  • New resident graduates or clinical specialists in their first 3-5 years of practice preferred
  • Or equivalent combination of education and experience
Job Responsibility
Job Responsibility
  • Provisions comprehensive clinical pharmacy services related to their area of practice to optimize safe, effective and cost-effective drug therapy
  • Participates as a member of an inter-disciplinary patient care team, provision of pharmacotherapeutic and pharmacokinetic consults, patient and provider education, and the development of best practice guidelines and policy related to pharmacotherapy
  • Serves as a leader for the department in their specialty area of practice, organizing appropriate departmental initiatives and providing education and teaching for pharmacy colleagues, providers and trainees at all levels of practice
  • Contributes to the overall objectives of the department as an integrated member of the pharmacy practice team
  • Provides comprehensive clinical pharmacy services for a specialized area of pharmacy practice
  • Works collaboratively with other clinicians and health-care providers to implement and maintain innovative disease or medication management programs and clinical pharmacy services
  • Participates in the development of global medication use management programs within the University, including clinical guidelines, critical pathways, disease management and drug use programs
  • Provides clinical leadership in area of specialty by serving as a mentor, coach and role model for all pharmacists in the department
  • Directs and supervises the work of technicians to ensure appropriate workflow as required
  • Conducts QA, MUE, or other research to document the value and contribution of clinical pharmacy services within area of specialization
  • Fulltime
Read More
Arrow Right

Clinical Pharmacy Specialist - Pediatric Infectious Disease

Provides pharmaceutical care for patients in a specialty clinical area. Supports...
Location
Location
United States , Hollywood
Salary
Salary:
Not provided
mhs.net Logo
Memorial Healthcare System
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Accredited Program: Pharmacy (Required)
  • Pharmacist License (PS LICENSE) - State of Florida (FL)
  • Doctor of Pharmacy or BS in pharmacy from an accredited School of Pharmacy
  • PGY2 residency or PGY1 residency/fellowship plus one (1) year of clinical experience in a specialty area or PGY1 residency/fellowship plus active board certification
  • Alternatively, active board certification plus three (3) years of clinical experience in a specialty area
Job Responsibility
Job Responsibility
  • Provides comprehensive clinical pharmacy services to a specialty patient population, including participation in interdisciplinary team rounds, selection and dosing of medication therapies, therapeutic drug monitoring and adjustment of drug therapies
  • Performs and documents clinical activities/interventions and their outcomes for use in drug therapy quality improvement efforts
  • Improves organizational performance by identifying and implementing clinical and/or safety initiatives
  • Serves as a preceptor and resource to the pharmacists, pharmacy interns and students
  • Reviews literatures, develops and deliver evidence-based drug information and education to multidisciplinary team and patients
  • Reviews, interprets and evaluates medication orders to optimize pharmacotherapy during order verification or entry in the electronic health record
  • Actively participates in the development, implementation and ongoing coordination of pharmacy residency research projects and/or mentors the resident
  • Serves as subject-matter expert for specialty patient population
  • Contributes expertise to multidisciplinary committees/teams in specialty area
What we offer
What we offer
  • $7,500 Sign on Bonus
  • Fulltime
Read More
Arrow Right

Infectious Diseases - Consultant

An exciting opportunity has arisen for a Substantive Consultant in Infectious Di...
Location
Location
United Kingdom
Salary
Salary:
109725.00 - 145478.00 GBP / Year
remediumpartners.com Logo
Remedium Partners
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Primary Medical Qualification (MBBS or equivalent)
  • Full GMC Registration with Licence to Practise
  • GMC Specialist Registration in Infectious Diseases or eligible within 6 months of interview
  • Appropriate Royal College Membership / MRCP or equivalent
  • Minimum 1 year NHS experience
  • Broad clinical experience in Infectious Diseases
  • Ability to independently manage complex referrals and acute infection cases
  • Experience in OPAT, antimicrobial management or inpatient infection services
  • Experience participating in multidisciplinary care pathways
Job Responsibility
Job Responsibility
  • Deliver high-quality Consultant-led Infectious Diseases services across inpatient and outpatient settings
  • Provide expert assessment, diagnosis and management of a broad range of infectious diseases, including complex and acute infections
  • Support and further develop the regional OPAT (Outpatient Parenteral Antimicrobial Therapy) service
  • Manage outpatient clinics including blood-borne virus services, tuberculosis, general infectious diseases, Lyme disease and PUO investigations
  • Work collaboratively with Microbiology, Pharmacy, Public Health, Respiratory Medicine, Cardiology, Oncology and other specialities
  • Participate in antimicrobial stewardship, infection prevention and clinical governance initiatives
  • Contribute to service redesign and development of integrated bedside-to-laboratory infection services
  • Participate in on-call rotas for Acute Medicine, Microbiology, or both, depending on experience and preference
  • Provide teaching, supervision and mentorship to junior doctors, medical students and allied healthcare staff
  • Participate in research, audit, quality improvement and innovation programmes
  • Fulltime
Read More
Arrow Right

Hepatology Account Manager

The Account Manager is pivotal in owning the B2B customer relationship in the la...
Location
Location
United States , Bronx; Hackensack
Salary
Salary:
162750.00 - 271250.00 USD / Year
us.gsk.com Logo
GSK
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's Degree in a relevant field
  • Valid driver's license
  • Account Manager 6: Minimum 5 years of biotech/pharmaceutical experience
  • Account Manager 7: Minimum 3 years of biotech/pharmaceutical experience
  • Travel Required: Up to 50% (based on specific district size)
  • Lift and/or move up to 35 pounds
Job Responsibility
Job Responsibility
  • Build partnerships with large-organized customers, incl. IDNs, Academic Centers, and key decision-makers (e.g. Chief Medical Officers, Pharmacy Directors, Infectious Disease Specialists and P&T Committee members)
  • Achieve and exceed sales targets within the assigned territory by developing, implementing, and executing an integrated business plan for key accounts to maximize sales
  • Identify and engage key influencers, ensuring designated customer interaction expectations are met, with a focus on top target customers
  • Plan and organize activities to achieve call metrics, optimizing coverage and frequency to key customers to maximize access and sales opportunities
  • Deliver comprehensive clinical brand presentations to physicians and other healthcare professionals, driving appropriate product utilization
  • Understand the healthcare delivery system within each assigned customer, including the physician hierarchy, key pharmacy personnel, and clinical nursing staff
  • Develop in-depth product and competitor knowledge, staying informed about local and regional market trends
  • Analyze local trends to identify long and short-term goals, crafting a robust product launch business plan
  • Collaborate with peers in the sales organization to share best practices and strategies
  • Provide feedback on marketing strategy, analyze the effectiveness of sales activities and territory performance, and develop territory plans with the Regional Sales Director, brand team, and other support partners to deliver exceptional customer experience
What we offer
What we offer
  • Competitive base salary
  • Annual bonus based on company performance
  • Flexible working options available for most roles
  • Learning and career development
  • Access to healthcare & wellbeing programmes
  • Employee recognition programmes
  • Health care and other insurance benefits (for employee and family)
  • Retirement benefits
  • Paid holidays
  • Vacation
  • Fulltime
Read More
Arrow Right

Hepatology Account Manager

The Account Manager is pivotal in owning the B2B customer relationship in the la...
Location
Location
United States , Philadelphia
Salary
Salary:
162750.00 - 271250.00 USD / Year
us.gsk.com Logo
GSK
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's Degree in a relevant field
  • Valid driver's license
  • Travel Required: Up to 50%
  • Account Manager 6: Minimum 5 years of biotech/pharmaceutical experience required
  • Account Manager 7: Minimum 3 years of biotech/pharmaceutical experience required
Job Responsibility
Job Responsibility
  • Build partnerships with large-organized customers, incl. IDNs, Academic Centers, and key decision-makers (e.g. Chief Medical Officers, Pharmacy Directors, Infectious Disease Specialists and P&T Committee members)
  • Achieve and exceed sales targets within the assigned territory by developing, implementing, and executing an integrated business plan for key accounts to maximize sales
  • Identify and engage key influencers, ensuring designated customer interaction expectations are met, with a focus on top target customers
  • Plan and organize activities to achieve call metrics, optimizing coverage and frequency to key customers to maximize access and sales opportunities
  • Deliver comprehensive clinical brand presentations to physicians and other healthcare professionals, driving appropriate product utilization
  • Understand the healthcare delivery system within each assigned customer, including the physician hierarchy, key pharmacy personnel, and clinical nursing staff
  • Develop in-depth product and competitor knowledge, staying informed about local and regional market trends
  • Analyze local trends to identify long and short-term goals, crafting a robust product launch business plan
  • Collaborate with peers in the sales organization to share best practices and strategies
  • Provide feedback on marketing strategy, analyze the effectiveness of sales activities and territory performance, and develop territory plans with the Regional Sales Director, brand team, and other support partners to deliver exceptional customer experience
What we offer
What we offer
  • Competitive base salary
  • Annual bonus based on company performance
  • Flexible working options available for most roles
  • Learning and career development
  • Access to healthcare & wellbeing programmes
  • Employee recognition programmes
  • Annual bonus
  • Eligibility to participate in our share based long term incentive program
  • Health care and other insurance benefits (for employee and family)
  • Retirement benefits
  • Fulltime
Read More
Arrow Right

Senior Clinical Research Associate II - FSP

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...
Location
Location
Turkey
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Extensive knowledge of clinical trial methodologies, ICH/GCP, Food and Drug Administration (FDA) and local country regulations
  • Monitoring Experience: Minimum 5 years relevant experience in clinical research site monitoring (preferably 3 years in Oncology)
  • Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
  • Global clinical trial experience
  • Must be fluent in English and in the native language(s) of the country they will work in
  • Significant travel (60-80%) within area is required. May require some international travel and some weekend travel
  • Valid driver’s license and passport required
  • Demonstrated knowledge of clinical research and development processes and ability to gain command of process details
  • Demonstrated knowledge of global and local regulatory requirements
  • Demonstrated understanding of key operational elements of clinical research (e.g., monitoring, data acquisition and cleaning, reporting, etc.)
Job Responsibility
Job Responsibility
  • Oversight of Monitoring Responsibilities and Study Conduct
  • Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and client standards to achieve project goals, timelines and quality
  • Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to database lock, ensuring relevant timelines and quality deliverables are met
  • During study conduct, serve as the primary point of contact for assigned investigator sites. Work in partnership with and/or escalate to the SCP to ensure quality of site delivery
  • Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites
  • Partner with SCP to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients
  • provide protocol training to, and address protocol related questions from the investigator site staff when required, including discussions on known/anticipated operational and clinical trial risks
  • Attend investigator meeting when required (virtual or F2F). Provide enrollment support and ensure progress by responding to site activation and recruitment issues from investigators. Partner with SCP and the study team to define and support recruitment initiatives at site level
  • Conduct onsite, remote/electronic monitoring as needed for study site initiation, routine monitoring and study site closure activities and ensure these are conducted accordance to the SMP, Standard Operating Procedures (SOPs) and commensurate with emerging issues and technologies
  • Monitor site level adverse events (AEs) and serious adverse events (SAEs) and collaborate with the Drug Safety Unit and follow-up with investigators sites, as needed, to bring SAE reports required information to resolution
What we offer
What we offer
  • Flexible work arrangements
  • Career growth and development
  • Supportive and inclusive environment
  • Diverse therapeutic areas and project exposure
  • Advanced Technology
Read More
Arrow Right

Senior Clinical Research Associate

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...
Location
Location
Brazil
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Extensive knowledge of clinical trial methodologies, ICH/GCP, Food and Drug Administration (FDA) and local country regulations
  • Monitoring Experience: Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology)
  • Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
  • Global clinical trial experience
  • Must be fluent in English and in the native language(s) of the country they will work in
  • Significant travel (60-80%) within area is required. May require some international travel and some weekend travel
  • Valid driver’s license and passport required
  • Demonstrated knowledge of clinical research and development processes and ability to gain command of process details
  • Demonstrated knowledge of global and local regulatory requirements
  • Demonstrated understanding of key operational elements of clinical research (e.g., monitoring, data acquisition and cleaning, reporting, etc.)
Job Responsibility
Job Responsibility
  • Oversight of Monitoring Responsibilities and Study Conduct
  • Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and client standards to achieve project goals, timelines and quality
  • Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to database lock, ensuring relevant timelines and quality deliverables are met
  • During study conduct, serve as the primary point of contact for assigned investigator sites. Work in partnership with and/or escalate to the SCP to ensure quality of site delivery
  • Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites
  • Partner with SCP to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients
  • provide protocol training to, and address protocol related questions from the investigator site staff when required, including discussions on known/anticipated operational and clinical trial risks
  • Attend investigator meeting when required (virtual or F2F). Provide enrollment support and ensure progress by responding to site activation and recruitment issues from investigators. Partner with SCP and the study team to define and support recruitment initiatives at site level
  • Conduct onsite, remote/electronic monitoring as needed for study site initiation, routine monitoring and study site closure activities and ensure these are conducted accordance to the SMP, Standard Operating Procedures (SOPs) and commensurate with emerging issues and technologies
  • Monitor site level adverse events (AEs) and serious adverse events (SAEs) and collaborate with the Drug Safety Unit and follow-up with investigators sites, as needed, to bring SAE reports required information to resolution
What we offer
What we offer
  • Flexible work arrangements
  • Career growth and development
  • Supportive and inclusive environment
  • Diverse therapeutic areas and project exposure
  • Advanced Technology
  • Fulltime
Read More
Arrow Right

Senior Clinical Research Associate

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...
Location
Location
Argentina
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Extensive knowledge of clinical trial methodologies, ICH/GCP, Food and Drug Administration (FDA) and local country regulations
  • Monitoring Experience: Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology)
  • Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
  • Global clinical trial experience
  • Must be fluent in English and in the native language(s) of the country they will work in
  • Significant travel (60-80%) within area is required. May require some international travel and some weekend travel
  • Valid driver’s license and passport required
  • Demonstrated knowledge of clinical research and development processes and ability to gain command of process details
  • Demonstrated knowledge of global and local regulatory requirements
  • Demonstrated understanding of key operational elements of clinical research (e.g., monitoring, data acquisition and cleaning, reporting, etc.)
Job Responsibility
Job Responsibility
  • Oversight of Monitoring Responsibilities and Study Conduct
  • Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and client standards to achieve project goals, timelines and quality
  • Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to database lock, ensuring relevant timelines and quality deliverables are met
  • During study conduct, serve as the primary point of contact for assigned investigator sites. Work in partnership with and/or escalate to the SCP to ensure quality of site delivery
  • Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites
  • Partner with SCP to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients
  • provide protocol training to, and address protocol related questions from the investigator site staff when required, including discussions on known/anticipated operational and clinical trial risks
  • Attend investigator meeting when required (virtual or F2F). Provide enrollment support and ensure progress by responding to site activation and recruitment issues from investigators. Partner with SCP and the study team to define and support recruitment initiatives at site level
  • Conduct onsite, remote/electronic monitoring as needed for study site initiation, routine monitoring and study site closure activities and ensure these are conducted accordance to the SMP, Standard Operating Procedures (SOPs) and commensurate with emerging issues and technologies
  • Monitor site level adverse events (AEs) and serious adverse events (SAEs) and collaborate with the Drug Safety Unit and follow-up with investigators sites, as needed, to bring SAE reports required information to resolution
What we offer
What we offer
  • Patient-focused in everything we do
  • Supportive and inclusive environment
  • Career growth and development
  • Flexible work arrangements
  • Diverse therapeutic areas and project exposure
  • Advanced Technology
Read More
Arrow Right