Oncology Pharmacy Clinical Specialist Job at Baptist Health (Boca Raton)

Clinical Pharmacy Specialist, Palliative Care Clinic

The Clinical Pharmacy Specialist, Palliative Care Clinic is responsible for prov...

Location

United States , Boston

Salary:

124000.00 - 159800.00 USD / Year

Dana-Farber Cancer Institute

Expiration Date

Until further notice

Requirements

Bachelor of Science in Pharmacy or Doctor of Pharmacy degree from an accredited college of Pharmacy
PGY2 residency in area of specialty (preferred) or PGY1 plus 2 years of clinical specialist experience (such as oncology, palliative care, anticoagulation) or 5 years of clinical specialist experience (such as oncology, palliative care, anticoagulation)
Must be licensed to practice pharmacy in the Commonwealth of Massachusetts
Pharmacists must attain board certification in their specialty area within 18 months of employment

Job Responsibility

Practices as a pharmacist in accordance with all federal, state, DFCI and Joint Commission policies, regulations, and standards
Ensures medication orders and/or prescriptions for appropriateness, accuracy and completeness based on patient-specific parameters and clinical data
Provides clinical consultation and evidenced based recommendations for treatment plans, supportive care, dose adjustments and monitoring plans to clinicians regarding pharmacotherapy needs for patients based on literature, clinical practice guidelines and institutional standards
Collaborates as a member of the pharmacy and interdisciplinary team through patient care related meetings including rounds, huddles, and case conferences as applicable
Provides comprehensive education to patients and caregivers receiving oncology related therapy including participation in the oral anticancer education program and review and maintenance of patient education materials
Documents clinical care activities in the EHR and effectively communicate all changes in care plan to the staff involved in patient care
Participates in scholarly and educational activities according to departmental expectations (e.g., in-services, drug use evaluation, resident precepting, clinical research, quality/process improvement, presents continuing education programs, guideline development)
Participates in clinical administrative duties such as pathways, beacon validation and active patient management, formulary request process and presentation to P&T committee(s), evaluate off label/exception review, REMS programs and other departmental or strategic initiatives
Participates in the development of policies, procedures, teaching documents, education and/or monitoring tools, workflow design, and other initiatives that will improve and/or expand the program
Other duties and projects as assigned

Fulltime

New

Oncology Pharmacy Clinical Specialist

The Pharmacy Clinical Specialist I is expected to take responsibility for establ...

Location

United States of America , Boca Raton

Salary:

118907.47 - 159218.11 USD / Year

Baptist Health

Expiration Date

Until further notice

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 to remain in this position
PGY1 residency with 2 years practice experience in area of specialty and BPS required
PGY2 residency must have BPS within 1 year of hire
Minimum Required Experience: 5 Years

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 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

What we offer

Sign-On Bonus: Up to $5,000
Career growth and development opportunities
Comprehensive health and wellness resources
Wellness program that can help employees eliminate their medical plan deductible
Tuition reimbursement

Fulltime

Senior Specialist Clinical Pharmacist - (Acute Care and Oncology)

An exciting opportunity has arisen for a Senior Specialist Clinical Pharmacist w...

Location

United Kingdom , Greater London

Salary:

Not provided

Remedium Partners

Expiration Date

Until further notice

Requirements

MPharm or BSc in Pharmacy
Registration with the GPhC
Minimum 1 year NHS experience
Acute hospital pharmacy experience
Strong clinical knowledge and patient-focused approach
Excellent communication and organisational skills

Job Responsibility

Deliver specialist clinical pharmacy services within Acute Care and Oncology services
Support safe and effective medicines optimisation
Provide expert pharmaceutical advice to multidisciplinary teams
Review and monitor patient medication plans
Support inpatient and outpatient clinical services
Participate in late shifts, on-call, and weekend service provision where required
Work collaboratively with consultants, nursing teams, allied healthcare professionals, and pharmacy colleagues
Contribute to patient-centred treatment planning and medicines governance
Participate in clinical audit, quality improvement initiatives, and medicine safety programmes
Maintain accurate clinical documentation and ensure compliance with professional standards

Fulltime

Clinical Pharmacist Specialist

As our Pharmacist Specialist, you’ll help our doctors and nurses safely prescrib...

Location

United States , Tacoma

Salary:

72.07 - 91.34 USD / Hour

American Nursing Care

Expiration Date

Until further notice

Requirements

Bachelors Of Science Pharmacy, upon hire or
Doctor Of Pharmacy Pharmacy, upon hire and
Residency completion or
3 years of clinical experience
Pharmacist: WA, upon hire and
Basic Life Support - CPR, upon hire and
Advanced Cardiac Life Support, upon hire and
Board Certified Ambulatory, within 36 - months or
Board Certified Cardiology, within 36 - months or
Board Certified Compound Strl, within 36 - months or

Job Responsibility

Meticulously review every prescription in your queue for safety, critically assessing for potential drug interactions, correct dosing, patient allergies, or any irregularities
Authorize prescriptions for the pharmacy technician, performing a final check before dispensing medication to the nursing station
Promote long and short-range planning to respond and integrate within the market, Region, and system
Work collaboratively with pharmacy peers to standardize clinical pharmacy systems when appropriate
Work, as directed by facility pharmacy leadership, on developing, coaching and mentoring pharmacy staff to maximize their scope of practice in the provision of clinical pharmacy services and scholarly activities across the continuum of care
Educate the medical staff regarding cost-effective, quality pharmaceutical care based on evidence based medicine and best practices
Participate in assigned committees relevant to their knowledge, experience and practice area
Assure that clinical pharmacy initiatives are in compliance with regulatory requirements

What we offer

medical, prescription drug, dental, vision plans, life insurance, paid time off (full-time benefit eligible team members may receive a minimum of 14 paid time off days, including holidays annually), tuition reimbursement, retirement plan benefit(s) including, but not limited to, 401(k), 403(b), and other defined benefits offerings

Fulltime

Senior Clinical Research Associate II - FSP

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...

Location

Turkey

Salary:

Not provided

Parexel

Expiration Date

Until further notice

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

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

Flexible work arrangements
Career growth and development
Supportive and inclusive environment
Diverse therapeutic areas and project exposure
Advanced Technology

Cancer Services Pharmacist

Hunter AHP are currently seeking an experienced Band 8a Cancer Services Pharmaci...

Location

United Kingdom , West London

Salary:

33.00 - 36.00 GBP / Hour

Hunter Gatherer AHP

Expiration Date

Until further notice

Requirements

GPhC-registered Pharmacist
BOPA SACT Passport
Minimum 12 months of oncology/SACT experience within an NHS hospital or similar setting
Strong knowledge of chemotherapy protocols, e-prescribing systems, and cancer pathway
Excellent clinical judgment, communication, and teamworking skills

Job Responsibility

Review, verify, and clinically screen chemotherapy prescriptions in line with BOPA standards
Provide specialist advice on systemic anti-cancer treatments to patients and healthcare professionals
Collaborate with multidisciplinary teams to ensure timely delivery of chemotherapy
Participate in audits, governance meetings, and cancer services improvement initiatives
Ensure compliance with local and national guidelines related to cancer therapy

What we offer

Competitive weekly pay
Flexible working arrangements to suit your lifestyle
Dedicated recruitment consultant offering one-to-one support
Opportunities for contract extensions and long-term placements
Access to other locum roles across London and the UK

Senior Clinical Research Associate

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...

Location

Argentina

Salary:

Not provided

Parexel

Expiration Date

Until further notice

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

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

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

Infectious Diseases - Consultant

An exciting opportunity has arisen for a Substantive Consultant in Infectious Di...

Location

United Kingdom

Salary:

109725.00 - 145478.00 GBP / Year

Remedium Partners

Expiration Date

Until further notice

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

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

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Oncology Pharmacy Clinical Specialist

Job Description

Job Responsibility

Requirements

What we offer

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