Specialist, Pharmacovigilance
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What you'll do
- Reviews written Adverse Event and Product Quality Complaint reports submitted to the drug manufacturer. Ensures timely and accurate transcription of data into the ConnectiveRx Quality Management System and that reports meet company and manufacturer requirements and standards. Conducts quality checks and ensures reports are submitted to the manufacturer as required.
- Monitors and audits potential sources of safety information under the guidance of the Manager, Pharmacovigilance. Sources may include recorded calls, claims, faxes, text messages, chat logs, and other records. Ensures all safety data identified is captured, recorded, and reported in compliance with company SOPs.
- Assists Pharmacovigilance teammates with tasks such as periodic reconciliation, records inspection, and internal audit activities.
- Supports internal audits and preparation for third-party audits under the supervision of the Manager.
- Performs other duties as assigned.
What they're looking for
- Associate degree or professional diploma in healthcare, pharmacy, or a medical-related field, or four years of equivalent relevant experience.
- Two to four years of experience in a medical, pharmacy, or healthcare environment (preferably in a call center or claims processing).
- Strong reading and verbal comprehension.
- Proficiency in English required; Spanish or other languages are a plus.
- Highly proficient in Microsoft Office applications including Word, PowerPoint, SharePoint, and Excel.
- Ability to clearly and concisely articulate medical and clinical information to manufacturer representatives.
Nice to have
- Medical call center or medical claims experience preferred.
- Quality Control or Quality Assurance experience is a plus.
- Spanish or other languages are a plus.
Summarised by NextRaise from the employer’s description, which follows in full below.
Full description from employer
Overview
Being on medication is tough enough. We want to make getting it the easy part. Getting prescriptions to patients has become increasingly complex. When things get messy along the prescription journey, pharmaceutical manufacturers rely on us to untangle the process and create a clear path—allowing patients to build trusting relationships with their medication brands.
We’re not only committed to taking the pain out of the prescription process, but we’re also devoted to bringing the brightest minds together under one roof. We bring together diverse voices—engineers, pharmacists, customer service veterans, developers, program strategists and more—all with one vision. Each perspective and experience makes ConnectiveRx better than the sum of its parts.
Under direct supervision of the department manager or supervisor, the Specialist, Pharmacovigilance is focused on meeting ConnectiveRx’s obligations for Drug Safety Monitoring and Reporting as required by the pharmaceutical manufacturers we support. The Specialist ensures that ConnectiveRx operates in a constant state of compliance with Pharmacovigilance activities.
Responsibilities
Reviews written Adverse Event and Product Quality Complaint reports submitted to the drug manufacturer. Ensures timely and accurate transcription of data into the ConnectiveRx Quality Management System and that reports meet company and manufacturer requirements and standards. Conducts quality checks and ensures reports are submitted to the manufacturer as required.
Monitors and audits potential sources of safety information under the guidance of the Manager, Pharmacovigilance. Sources may include recorded calls, claims, faxes, text messages, chat logs, and other records. Ensures all safety data identified is captured, recorded, and reported in compliance with company SOPs.
Assists Pharmacovigilance teammates with tasks such as periodic reconciliation, records inspection, and internal audit activities.
Supports internal audits and preparation for third-party audits under the supervision of the Manager.
Performs other duties as assigned.
Qualifications
Education/Degree Requirements
Associate degree or professional diploma in healthcare, pharmacy, or a medical-related field, or four years of equivalent relevant experience.
Experience
Two to four years of experience in a medical, pharmacy, or healthcare environment (preferably in a call center or claims processing).
Medical call center or medical claims experience preferred.
Quality Control or Quality Assurance experience is a plus.
Knowledge
Strong reading and verbal comprehension.
Proficiency in English required; Spanish or other languages are a plus.
Highly proficient in Microsoft Office applications including Word, PowerPoint, SharePoint, and Excel.
Ability to clearly and concisely articulate medical and clinical information to manufacturer representatives.
Skills
Strong problem-solving skills with the ability to resolve issues independently or escalate when needed.
Ability to organize and prioritize work across multiple systems to meet reporting deadlines.
Ability to learn and successfully utilize Quality System software.
Accurate transcription of text or audio information.
Effective communication of ideas and concepts.
Responsive, attentive, patient, respectful, and professional with colleagues, leadership, and manufacturer contacts.
Strong analytical skills, results orientation, and attention to detail.
Competencies
Process Knowledge: Identifies, documents, and monitors key processes needed to achieve business results. Drafts procedures that comply with processes and implements process improvement recommendations.
Decision Quality: Makes appropriate and timely decisions using analysis, knowledge, and judgment, even with incomplete information. Evaluates and prioritizes factors to reach sound solutions.
Service Orientation: Anticipates and addresses customer needs, sometimes before they are voiced. Provides thoughtful, empathetic, prompt, and courteous service to internal and external customers.
Consultation Communication: Provides guidance to stakeholders, offering solutions based on best practices and supporting organizational objectives such as culture change, restructuring, or training.
Travel or Physical Requirements
None
Compliance Requirements
Adhere to all company policies, procedures, and training consistent with ConnectiveRx’s Information Security and Compliance Programs, including SOC1, SOC2, PCI, and HIPAA.
Maintain strict compliance with company and client policies regarding business rules and ethics, as well as all applicable laws and regulations.
Compensation & Benefits: This position offers opportunities for a bonus (or commissions), with total compensation varying based on factors such as location, relevant skills, experience, and capabilities.
Employees at ConnectiveRx can access comprehensive benefits, including medical, dental, vision, life, and disability insurance. The company regularly reviews and updates its health, welfare, and fringe benefit policies to ensure competitive offerings. Employees may also participate in the company’s 401(k) plan, with employer contributions where applicable.
Time-Off & Holidays: ConnectiveRx provides a flexible paid time off (PTO) policy for exempt employees, covering sick days, personal days, and vacations. PTO is determined based on an employee’s first year of service. Employees also receive eight standard company holidays and three floating holidays annually, with prorations applied in the first year.
The company remains committed to providing competitive benefits and reserves the right to modify employee offerings, including PTO, STO, and holiday policies, in accordance with applicable laws and regulations.
Posted Salary Range
USD $19.51 - USD $25.85 /Hr.Company
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