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Pharmacovigilance Coordinator

Pharmiweb
2-4 years
preferred by company
10 Jan. 16, 2026
Job Description
Job Type: Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Pharmacovigilance Coordinator – Post Marketing (FSP, Sponsor-Dedicated)

Company: ICON Strategic Solutions
Location: Brazil (Remote / Home-Based)
Employment Type: Full-Time
Experience Level: Mid-Level
Start Date: 14 January 2026
Application Deadline: 13 February 2026
Salary: Competitive (Commensurate with Experience)


About ICON Strategic Solutions

ICON plc is a global leader in healthcare intelligence and clinical research, partnering with biopharmaceutical companies to accelerate the development of innovative medicines. With a strong commitment to inclusion, scientific excellence, and operational quality, ICON empowers professionals to make a meaningful impact on patient safety worldwide.


About the Role

ICON Strategic Solutions is seeking a Pharmacovigilance Coordinator – Post Marketing to support sponsor-dedicated pharmacovigilance activities within a Functional Service Provider (FSP) model. This role is ideal for professionals experienced in drug safety operations who are passionate about patient safety, regulatory compliance, and cross-functional collaboration in a global environment.

You will play a critical role in ensuring timely and accurate safety monitoring, post-marketing surveillance, and regulatory reporting for marketed products, while supporting global pharmacovigilance standards.


Key Responsibilities

Pharmacovigilance Operations

  • Coordinate day-to-day post-marketing pharmacovigilance activities, ensuring accurate and timely adverse event processing

  • Support safety data collection, review, analysis, and submission to global health authorities

  • Ensure compliance with international pharmacovigilance regulations and internal SOPs

Cross-Functional Collaboration

  • Work closely with clinical operations, regulatory affairs, and sponsor teams to streamline safety processes

  • Support inspection readiness and audit activities related to safety reporting

Quality & Compliance

  • Maintain high standards of data quality and documentation accuracy

  • Assist in continuous process improvement initiatives within pharmacovigilance operations

Team Support & Leadership Exposure

  • Contribute to training activities and knowledge sharing within the pharmacovigilance team

  • Support project-level coordination and safety deliverables in a sponsor-dedicated environment


Qualifications & Experience Required

Education

  • Bachelor’s degree in Life Sciences, Pharmacy, Medicine, Nursing, or a related discipline

Experience

  • Minimum 2–4 years of experience in pharmacovigilance, drug safety, or post-marketing surveillance

  • Prior experience in clinical trials and/or post-authorization safety activities is preferred

  • Experience working within CRO, sponsor-dedicated, or FSP models is an advantage

Skills & Competencies

  • Strong knowledge of global pharmacovigilance regulations and guidelines (ICH, GVP, FDA, EMA)

  • Excellent organizational and time-management skills with strong attention to detail

  • Ability to manage multiple priorities in a remote, global work environment

  • Strong written and verbal communication skills

  • Fluency in English (reading, writing, and speaking)


Why Join ICON?

  • Work remotely with a globally recognized clinical research organization

  • Gain exposure to sponsor-dedicated post-marketing pharmacovigilance programs

  • Competitive compensation and country-specific benefits focused on well-being and work-life balance

  • Access to global learning, career development, and internal mobility opportunities

  • Inclusive and diverse workplace committed to equal opportunity and professional growth


ICON is an equal opportunity employer and is committed to creating an inclusive, discrimination-free workplace. All qualified applicants will receive fair consideration regardless of race, religion, gender, age, disability, or any other legally protected status.


Apply now on thepharmadaily.com to advance your career in pharmacovigilance and contribute to global patient safety with ICON Strategic Solutions.