45 Results for

Pharmacovigilance Specialist Jobs in the United States

Jobs

Lawrenceville, NJ10 days ago

Responsibilities:Data Analytics and ReportingBuild and continuously improve data analytics through supporting models that provide insights into efficiency, quality, stakeholder feedback, and key performance indicators to drive timely and informed decision making. The PV Analytics and Reporting Specialist, PV Analytics Center of Excellence applies a combination of life sciences strategy, leadership, and reporting/visualization experience to drive successful servicing of information needs across PS.

Foster City, CA11 days ago

$46–$46 Per Hour

Performs routine and non-routine daily case management activities independently and provides direction as needed to junior staff assists junior staff as needed. Actively participates in internal and cross functional teams as a representative of functional group; may lead functional work streams as required.

Worcester, MA11 days ago

Where relevant, oversee or collaborate with specialty sections such as Pediatric & Adolescent Gynecology, Complex Family Planning, and Complex Benign Gynecology/Minimally Invasive Gynecologic Surgery, and other subspecialty divisions including Maternal-Fetal Medicine, Gynecologic Oncology, Reproductive Endocrinology and Infertility, and Urogynecology. The largest division in the Department, including academic specialists in general obstetrics and gynecology, family planning specialists, complex benign gynecology/minimally invasive gynecologic surgery specialists, pediatric and adolescent gynecology specialists, and advanced practice clinicians.

9 days ago

Remote

$72,000–$100,000 Per Year

Assess ICSRs for individual adverse event terms signifying seriousness and expectedness relative to the product label while also referencing guidance documents provided by regulatory authorities on assessing seriousness. At least 2 years’ experience working in Pharmacovigilance, a Contract Research Organization (CRO) or other related scientific area; with specific experience working with Medical Devices, preferred.

9 days ago

Remote

$105,000–$120,000 Per Year

Trenton, NJ30+ days ago

The PV Analytics and Reporting Specialist, PV Analytics Center of Excellence contributes to the ongoing development, implementation, and successful execution of the scientific, operational, and regulatory reporting efforts in line with the overall WWPS needs. The PV Analytics and Reporting Specialist, PV Analytics Center of Excellence applies a combination of life sciences strategy, leadership, and reporting/visualization experience to drive successful servicing of information needs across WWPS.

Boston, MA30+ days ago

Full-time

Responsibilities and DutiesReviews adverse event information received for completeness and consistency, triage of cases and initiates case follow-up activities with internal medical team, other cross-functional team members, and safety vendor, as applicable. At Rhythm we are dedicated to transforming the lives of patients living with rare neuroendocrine diseases by rapidly advancing care and precision medicines that address the root cause.

Puyallup, WA30+ days ago

Full-time
Employee

MultiCare Cancer Institute is a physician-led, multi-specialty group within MultiCare Health System, delivering integrated hematology, oncology, radiation, surgical and supportive care across Washington state. Maintains, coordinates and manipulates provider clinic schedule to accommodate surgical cases, CME, vacation, court appearance, attorney depositions and all other meetings for the provider, using both Epic and MS Outlook programs.

New!

Foster City, CA4 days ago

$44.60–$46.90 Per Hour

Foster City, CA27 days ago

Full-time

Onsite Position - Foster City Job Overview/Summary: As part of a broader PS team, performs operational job responsibilities that ensure compliance of pharmacovigilance activities including the collection, review, evaluation, processing, and submission of adverse event (AE) information received by Gilead PS Actively participates in internal and cross functional teams as a representative of functional group; may lead functional work streams as required Identifies issues and proactively proposes possible solutions to management May assist management in obtaining resolution Provides input into team trainings and may lead trainings May lead functional projects Job Responsibilities: Performs routine and non-routine daily case management activities independently and provides direction as needed to junior staff assists junior staff as needed Leads training and/or on-boarding activities Leads projects of high complexity Participates in cross-functional projects may represent functional area at project meetings May serve as a point of contact to other functions inside and outside of the organization May develop and/or assist with quality review of data for the applicable functional area

Princeton, NJ30+ days ago

Full-time

It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). The position carries full accountability for end-to-end safety case processing, including regulatory submissions, hands-on work within the safety database, and CAPA management and coordination.

Bridgewater, NJ30+ days ago

Responsible for the collection, data entry, routing, follow-up, and timely reporting/submission of safety information related to drug products from a variety of sources (clinical trial, spontaneous, literature), both U.S. and foreign, in compliance with SOPs, US regulations, and international regulations. Ability to make quick assessments to meet strict deadlines.

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Seal Beach, California3 days ago

Responsibilities: Serves as an essential link between Dendreon Medical Affairs and healthcare professionals (HCPs) and non-HCPs (including patients and payors); assisting with the appropriate dissemination of scientific information, while continuously monitoring enquiry trends and metrics and proactively identifying unmet content needs and product trends to the wider Dendreon audience. Recognizes and obtains pertinent patient level data on, and accurately transmits, adverse events or product complaints to appropriate internal pharmacovigilance (PV) department within required timelines (within 24 hours of awareness); maintains a record of all external Medical Information interactions via the IRMS database.

Summit, New Jersey30+ days ago

Contractor

We implement multi-channel patient programs across U.S., and we are looking for an experienced Nurse Specialist to successfully deliver new and existing projects and to bring experience, energy and expertise to the delivery of our patient-centric programs. You will be part of a dedicated Nurse Services team that serves as the frontline of patient engagement, providing support via phone and digital channels, helping patients understand their treatment, overcome barriers, and stay on track with their care plans.

Atlanta, GA30+ days ago

$166,400–$212,000 Per Year

In addition to being the country’s largest national network and the industry’s most comprehensive portfolio of radiopharmaceuticals, we offer best-in-class service with unmatched accuracy and reliability, access to breakthrough radiopharmaceuticals to drive new revenue streams and clinical differentiation and 24/7 access to nuclear pharmacists who routinely consult on patient care and best practices. Centralized nuclear pharmacies specialize in servicing multiple customers within their geographic markets while driving cost control, material efficiencies and broad product access for the direct benefit of their customers.

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Savannah, GA1 day ago

The Parts Sales Specialist assists customers and technicians in securing parts and supplies, aiming to meet monthly sales and profit targets. The role involves maintaining positive customer relationships, ensuring a clean work environment, and entering sales data into inventory systems.

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Albuquerque, NM1 day ago

Responsibilities include assessing claim compensability, documenting activities, managing reserves, ensuring timely benefit payments, and participating in legal proceedings. The Claims Specialist provides expert handling of complex workers' compensation claims, focusing on coverage, investigation, evaluation, negotiation, and litigation management in accordance with laws and policies.

Orange, California30+ days ago

Listed among America’s Best Hospitals by U.S. News & World Report for 23 consecutive years, UCI Medical Center provides tertiary and quaternary care and is home to Orange County’s only National Cancer Institute-designated comprehensive cancer center, high-risk perinatal/neonatal program and American College of Surgeons-verified Level I adult and Level II pediatric trauma center, gold level 1 geriatric emergency department and regional burn center. *Misconduct Disclosure Requirement: As a condition of employment, the final candidate who accepts a conditional offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; received notice of any allegations or are currently the subject of any administrative or disciplinary proceedings involving misconduct; have left a position after receiving notice of allegations or while under investigation in an administrative or disciplinary proceeding involving misconduct; or have filed an appeal of a finding of misconduct with a previous employer.

Flagstaff, Arizona17 days ago

$38,628–$48,285 Per Year

Provide prompt and accurate communications and/or responses to questions regarding gift processing and data entry related inquiries from members of the division, alumni, donors, and other colleges and departments across NAU. Database records maintenance, strong customer service skills, problem solving and analytical skills, ability to work independently or collaboratively on a team, proficiency in Microsoft Office Suite (Excel, Word).

Salina, Kansas12 days ago

$118,000–$170,000

We are seeking an experienced Informatics Pharmacist to support and optimize pharmacy systems, medication safety initiatives, and clinical workflows within a hospital setting. This role is ideal for a clinically driven pharmacist interested in advancing pharmacy technology, automation, and operational efficiency.

Orlando, FL30+ days ago

Assist in the day-to-day operations of the Compliance Department including hotline responses, internal controls, safety reporting/Pharmacovigilance, document control, training, risk management, vendor risk analysis, business continuity, nonconformance, CAPA program, security questionnaires, and trend reporting. + Certified Professional in Project Management Professional (PMP), Certified Healthcare Compliance (CHC), Certified HIPAA Professional (CHP), Certified Information Systems Security Professional (CISSP), Information Systems Manager (CISM), Certified Information Systems Auditor (CISA), or other relevant certifications preferred.

South San Francisco, CA30+ days ago

$209,700–$389,500 Per Year

Serving as lead legal counsel for global development programs involving innovative scientific initiatives with external collaborators including pharmaceutical manufacturers, digital or device developers, academic institutions, research collaborative groups, and government entities; + Proactively identifying and addressing enterprise-wide legal issues, based on an excellent understanding of business strategy and goals, fostering trusted relationships with client groups, advising leaders in the R&D and Medical Affairs organizations, serving as a standing or ad hoc member of business or leadership team(s); and. + Consulting and collaborating with internal and external stakeholders and subject matter experts to support the above activities, our internal legal colleagues (IP, transactional, privacy, and product attorneys) as well as VP-level business leadership, regulatory experts, ethics experts, and legal policy committee members.

New!

Kings County, NY5 days ago

Remote

$80–$87 Per Hour

Navitas Healthcare, LLC" is seeking an experienced and highly organized Program Manager / Certification Specialist to support the development, implementation, and accreditation management of a nationally recognized breast care accreditation program. This role will lead accreditation readiness initiatives, oversee program development activities, coordinate multidisciplinary teams, and manage quality improvement and regulatory compliance efforts within a healthcare environment.

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Bangor, ME1 day ago

They share personal recovery experiences, promote resiliency, collaborate with care teams and caregivers, and connect youth to community resources. The Youth Peer Support Specialist is a full-time position serving the Bangor area, supporting youth aged 18-30 with mental health diagnoses in recovery.

Seattle, WA7 days ago

Nearly 29,000 healthcare professionals, researchers, and educators work in the UW Medicine family of organizations that includes: Harborview Medical Center, UW Medical Center - Montlake, UW Medical Center - Northwest, Valley Medical Center, UW Medicine Primary Care, UW Physicians, UW School of Medicine, and Airlift Northwest. + Independently manage a complex patient caseload, including diagnostic audiometry, immittance testing, otoacoustic emissions, hearing aid evaluations, hearing aid fittings, verification, follow-up care, troubleshooting, and patient education.

New Brunswick, NJ30+ days ago

o Carries out functions of the GxP-ITQA as directed including but not limited to: Review and approval of key computer system Validation Life Cycle (VLC) deliverables; Review and approval of test scripts and defects associated with computer system validation; Oversight of key Software Development Life Cycle (SDLC) process such as incident, problem, change, release, etc. • Project management practices and techniques; • Experience with automated testing practices and tools preferred; • Computer hardware, software including MS Office and MS Project; • External and internal inspections support a plus; • Excellent analytical, interpersonal, and communication skills, including written and verbal communication.

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Port Charlotte, FL2 days ago

The Advanced Clinical Pharmacist will focus on critical care and will coordinate and assist with the development, implementation and maintenance of clinical pharmacy services, including but not limited to trauma/surgical, medical, neuro, and cardiovascular surgery intensive care services lines. Strong knowledge of critical care therapeutics, excellent communication skills, ability to work under pressure, and strong interpersonal skills for team collaboration.

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Danbury, CT6 days ago

$45.93–$85.29 Per Hour

Performs non-invasive procedures including EKG, Holter & TTM hook up, Holter Analysis Scanning, SAECG, and independently performs all forms of Exercise stress testing including Nuclear Cardiology Exercise Stress Testing, including the administration of pharmacology involved in pharmalogical stress testing. Summary: To safely operate cardiac diagnostic equipment, supervise and compile data on patients during cardiac diagnostic procedures to obtain optimal results and data processing for the general purpose of diagnosing heart disease.

Wilmington, North Carolina9 days ago

The Imaging Specialist partners with Clinical Engineering, Imaging Services, vendors, and clinical teams to minimize equipment downtime and support high-quality patient care. What We Offer: The Imaging Specialist is responsible for maintaining, troubleshooting, repairing, and supporting biomedical and diagnostic imaging equipment across the organization.

Irvine, California30+ days ago

$60–$66.92 Per Hour

Develop, review, and update clinical design control documents including providing advice and guidance to product development team on development of technical summaries, clinical risk assessments, product training, instructions for use, design of validation protocols and reports, usability protocols and reports, design and application of FMEAs (Failure Modes and Effects Analysis), for technical and clinical documentation in product development. * Design, review and/or conduct literature searches and complete literature reviews for design concept, product development, protocol preparation, clinical risk assessments and/or clinical evaluation reports.

Helena, MT7 days ago

$38–$50

If you thrive in collaborative environments and want your work to directly impact the quality of care patients receive every day, this role offers the visibility, influence, and purpose you’re looking for. The Staff Pad has partnered with a leading healthcare system in beautiful Helena, Montana to hire an experienced and passionate Patient Safety Specialist.

Tuscaloosa, Alabama30+ days ago

Overview: The Quality Specialist RN performs a variety of functions under the Quality Department Scopes of Work which include but are not limited to: Performance Improvement: Collection, analysis, data reporting and facilitation of performance improvement methodologies for assigned projects. Generates reports and communicates results and activities to administration, medical staff and other internal and external parties to support organizational improvement initiatives.

New Haven, Connecticut11 days ago

Supports Q&S operations by utilizing appropriate benchmarking and performance resources (i.e., Centers for Medicare Services (CMS) and QualityNet, Vizient, Agency for Healthcare Quality (AHRQ), LeapFrog, US News & World Report, and clinical registries) to formulate integrated clinical and operational data analyses in Nursing. Stays abreast of changes that impact Nursing performance in reported measures including, but not limited to Centers for Medicare Services (CMS) and QualityNet, Vizient, Agency for Healthcare Quality (AHRQ), LeapFrog, US News & World Report, and clinical registries.

Schaumburg, IL30+ days ago

Full-time

The job responsibilities of this position may include, but are not limited to: - Own, plan, author, and maintain Post-Market Surveillance documentation, including Post-Market Surveillance (PMSP/PMSR), Periodic Safety Update (PSUR), Post-Market Clinical Follow-Up (PMCFP/PMCF). - Familiarity with relevant international regulatory requirements and guidance documents for medical devices, including MEDDEV 2.7/1 revision 4. - Familiarity applying research methodology and information management.

New!

Port Charlotte, FL1 day ago

$21.64–$31.17 Per Hour

This role involves developing and implementing individualized exercise programs for elderly or frail individuals, monitoring vital signs, and collaborating with healthcare professionals to ensure safe, effective wellness plans. Requirements include a Bachelor’s degree in Exercise Science/Physiology/Kinesiology, CPR certification, valid Florida driver’s license, and experience with older populations preferred.

30+ days ago

$40,000–$50,000

With support from leading healthcare investors, and impactful leaders like you, we'll continue to provide high-quality patient-centered care for the evaluation and management of brain health conditions and deliver exceptional client and family outcomes for years to come. With a heavy focus on clinical quality and safety in all that we do, we've accomplished excellent outcomes for our clients: 92% of clients report an improvement against their cognitive goals in only 3 weeks after working with Isaac Health.

New!

Gardner, Massachusetts6 days ago

$18–$18.36 Per Hour

Organizational ExpectationsBehavioral AttributesThe following behavioral attributes are required: achievement motivation, concern for order, flexibility, initiative, self-confidence, customer service oriented, interpersonal effectiveness, teamwork, analytical thinking and information seeking. Performs frequent or constant patient observations as directed, documents patient location and behavior, and promptly reports/communicates any patient behaviors and safety concerns to the nursing staff to support care planning and risk mitigation.

Gardner, Massachusetts13 days ago

$18–$18.36 Per Hour

New!

Gardner, Massachusetts6 days ago

$18–$18.36 Per Hour

New!

Olympia, WA4 days ago

Providing medical inputs to case processing team + Raising appropriate follow-up queries for relevant information from the reporter/HCP (Health Care Professional) + Review and verify appropriate selection of adverse events from source documents, assign appropriate Medical Dictionary for Regulatory Activities (MedDRA) code, review narrative + Identify and resolve case issues, coordinate with client therapeutic/legal team + Provide guidance to junior physicians on case assessment methodologies **Periodic reports (as applicable)** + Reviewing and/ or authoring of aggregate reports for medical content and consistency in accordance with client requirements and SOPs + Providing medical inputs into, and supporting the preparation of key regulatory documents including but not limited to, Periodic Benefit-Risk Evaluation Reports (PBRERs)/ Periodic Safety Update Reports (PSURs), Signal Evaluation Reports (SERs), Health Authority (HA) response documents, Development Safety Update Reports (DSURs), Clinical Overviews (COs), Addendum to Clinical Overview (ACOs), Health Hazard Evaluation reports (HHEs), etc. **Key Accountabilities:** **General** + Maintaining a good working knowledge of the Adverse event/Safety profile of assigned products, labeling documents, data handling conventions, client's guidelines and procedures, and global drug safety regulations and guidelines + Maintaining an awareness of global regulatory requirements, reporting obligations and organizing workload to ensure compliance with internal and regulatory timelines for adverse event reporting + Communicating and discussing issues related to review process with Line Manager/ Project Leader/Designee + Interacting with internal and external stakeholders for resolving issues + Attending and/ or presenting at client/cross functional meetings along with other stakeholders.

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Wake Forest, NC6 days ago

Communication: Exceptional cross-functional leadership and client-facing presentation skills; ability to articulate the value of a tech-enabled clinical contact center to diverse stakeholders. AI & Innovation: Implement and optimize AI-augmented workflows (e.g., intelligent triage, automated AE capture, generative drafting, and sentiment analysis) to drive efficiency, accuracy, and market competitiveness.

New!

Maple Grove, MA4 days ago

Remote

Conduct signal detection activities to identify potential safety concerns associated with drug products and collaborate with cross-functional teams to mitigate risks. Support regulatory submissions and interactions with health authorities related to drug safety, including responses to safety-related inquiries and requests for information.

San Diego, CA30+ days ago

$280,000–$300,000 Per Year

The Senior Director, Drug Safety Operations will be provide leadership and direction to the Drug Safety operations for adverse event case management, support of study teams and projects, oversight of maintenance of drug safety database, and collaboration to support risk management and pharmacovigilance, vendor oversight activities and ensures compliance and operational excellence for PV related activities. Support the Head of Clinical Safety & Pharmacovigilance in the review and development of written materials including clinical trial protocols, Informed Consent Forms, Case Report Forms, adverse event (AE)/ serious adverse event {SAE) reporting forms, Clinical Study Reports, and Investigator's Brochures (including Reference Safety Information determinations).

Princeton, NJ30+ days ago

Full-time

This individual will also support the clinical R&D team in the oversight of PV service vendors and partners and will need to maintain medical knowledge, as well as current knowledge of drug safety and pharmacovigilance regulations, pharmacovigilance practices, safety surveillance and risk-management practices. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs).

New!

Olympia, WA5 days ago

$142,400–$224,100 Per Year

Inspection Preparation and Management:** The CQOM is responsible for maintaining current regulatory inspection knowledge as it relates to Good Clinical Practice (GCP) inspections by regulatory agencies worldwide, especially those conducted by key authorities such as the USA Food and Drug Administration, European Medicines Agency, UK Medicines and Healthcare products Regulatory Agency, as well as other established and emerging authorities. + Develops the strategy for management/support for GCP inspections of Company products to ensure that all phases of Regulatory Health Authority inspections (i.e. inspection preparation, management and follow up) are handled consistently, professionally and proactively and result in outcomes that demonstrate the Company's dedication to regulatory compliance.

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Pharmacovigilance Specialist Jobs in the United States

Pharmacovigilance (PV) Analytics and Reporting Specialist ECLARO

Drug Safety Public Health Specialist - II Careers Integrated Resources Inc

Division Chief-Academic Specialists in General Obstetrics & Gynecology, UMass Memorial Medical Group UMass Memorial Health

Pharmacovigilance Specialist-Registered Nurse Safetycall International

Pharmacovigilance Specialist-Pharmacist Safetycall International

C08 - MEDICAL AND REGULATORY AFFAIRS / PHARMACOVIG - PHARMACOVIGILANCE SPECIALIST TechDigital Corporation

Pharmacovigilance (PV) Specialist Rhythm Pharmaceuticals

Scheduling Coordinator Specialist Clinic MultiCare Health System

Drug Safety Public Health Specialist - II Iconma

Drug Safety Public Health Specialist - II* LanceSoft Inc

PV Operations Specialist Systimmune

Drug Safety Specialist III OQSIE

Medical Information Specialist Dendreon Corporation

Nurse Specialist - Patient Support Programs Atlantis Health

Sr. Consultant, Nuclear Product Sales Specialist Cardinal Health

Parts Sales Specialist MHC Kenworth

Claims Specialist New Mexico Mutual

Clinical Excellence Specialist - F/T - Days University of California, Irvine

Data Entry Specialist Northern Arizona University

Perm - Pharmacist - Informatics Specialist MedlinkHealth Anesthesia

SOC2 Audit Specialist - (Heathcare/Pharma) AssistRx

Senior Counsel Specialist, Assistant General Counsel- R&D Law Group Genentech

Program Manager / NAPBC Certification Specialist - 100% Remote NavitasPartners

Youth Peer Support Specialist Northern Light Health

Audiologist Specialist 3 University of Washington

Validation - IT Quality Compliance Specialist/Analyst TechDigital Corporation

Pharmacy Clinical Specialist Pharmacist HCA Healthcare

RN Nurse Specialist Per Diem- Stress Testing department- Danbury, CT Northwell Health

Imaging Specialist Novant Health

Sr Specialist, Clinical Development Roth Staffing Companies

Patient Safety & Quality Specialist (RN) The Staff Pad

Quality Specialist - RN - Quality Management DCH Health System

Service Line Lead Quality and Safety Specialist - Women's Health Yale New Haven Health

Senior Post-Market Surveillance Specialist BISCO, Inc.

PACE Exercise Specialist-PACE Program-Port Charlotte CHAPTERS HEALTH SYSTEM

Healthcare Contact Center Specialist (Sales experience required) Isaac Health

Safety Specialist, Mental Health Unit, 32-Hours, Evening, 3:00 pm - 11:30 pm, Every other weekend/holiday Heywood Hospital

Safety Specialist, ER, Per Diem, Variable shifts, Availability for all days and all shifts Heywood Hospital

Safety Specialist, Watkins 2, 24-Hours, Evenings, 3:00 PM-11:30 PM, Every other weekend/holiday Heywood Hospital

Senior Physician, Patient Safety (Senior Drug Safety Physician) Parexel

Senior Director, Medical Patient Support Services Syneos - Commercial - Prod

Drug Safety Pharmaceutical Consultants Pharmavise Corporation

Senior Director, Drug Safety Operations Arrowhead Pharmaceuticals

Drug Safety Physician Systimmune

Clinical Quality Operations Manager, Oncology Merck

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