Pharmacovigilance Associate/Senior PV Associate at ICON plc
Job Details:
| Job Title | Pharmacovigilance Associate/Senior PV Associate |
|---|---|
| Company | ICON plc |
| Location | Chennai, India |
| Experience | 1 to 2 Years |
| Salary | Not disclosed |
| Posted on | October 4, 2024 |
| Key Skills | Good communication, time management, flexibility, problem solving |
About ICON plc
ICON plc is a global leader in healthcare intelligence and clinical research, specializing in advancing healthcare by conducting innovative clinical trials. With a strong emphasis on a diverse and inclusive work environment, ICON fosters an atmosphere where employees can thrive and make meaningful contributions to shaping the future of clinical development. If you’re passionate about safety and patient care in the pharmaceutical industry, joining ICON will provide you with opportunities to make a global impact. Pharmacovigilance Associate/Senior PV Associate at ICON plc
Role Overview
As a Pharmacovigilance Associate or Senior PV Associate, you will be at the forefront of ensuring patient safety by closely monitoring, analyzing, and reporting adverse events. Based in Chennai, India, this role is an excellent opportunity for professionals who have experience in pharmacovigilance and want to grow within a reputable global company. Pharmacovigilance Associate/Senior PV Associate at ICON plc
Key Responsibilities
Here are the primary responsibilities of a Pharmacovigilance Associate at ICON:
- Safety Event Processing: You will review and process safety events from various sources, including pre-marketing, post-marketing, medical device, and drug-related data.
- Literature Review: You will analyze both abstracts and full articles to identify relevant safety information for pre- and post-marketed products.
- Data Accuracy: Maintaining accurate data is essential. You’ll generate data listings from safety databases, ensuring precision and compliance.
- Adverse Event Follow-Up: You will conduct follow-up communications (phone or written) regarding adverse events, in accordance with specific client requirements.
- Safety Documentation: Ensuring the accuracy of safety tracking systems, managing project files, and supporting timely documentation are essential tasks in this role.
- Collaboration: You’ll collaborate with investigational sites, sponsors, ICON Medical Monitors, and project managers to address safety issues as they arise.
- Post-Marketing Activities: Support post-marketing safety efforts, including the creation of Pharmacovigilance System Master Files (PSMF), Risk Management Plans (RMP), and Periodic Benefit-Risk Evaluation Reports (PBRER).
- Signal Detection: Assist the Safety Scientist in detecting signals and conducting risk management activities to ensure patient safety.
- Audits & Inspections: You’ll be involved in supporting audits and inspections to ensure compliance with the project’s safety management plan.
Qualifications and Skills
For this position, the ideal candidate will have:
- Experience: At least 1 year of experience in a pharmaceutical or Contract Research Organization (CRO) environment with a focus on pharmacovigilance.
- Education: A background in life sciences or a related field is preferred.
- Skills: Excellent verbal and written communication skills, strong organizational abilities, and attention to detail. Proficiency in English is essential.
- Teamwork: Ability to work both independently and as part of global teams. A collaborative attitude is key to success in this role.
Why Work at ICON?
ICON values its employees and offers a comprehensive benefits package that is designed to support well-being and work-life balance. Benefits include:
- Annual Leave: Generous leave entitlements to ensure you can recharge.
- Health Insurance: Health insurance plans tailored to meet the needs of you and your family.
- Retirement Planning: Access to retirement planning options to help secure your financial future.
- Employee Assistance Program: Global Employee Assistance Program offering 24/7 support for you and your family.
- Additional Perks: Life assurance, flexible optional benefits like discounted gym memberships, health assessments, and travel passes. Pharmacovigilance Associate/Senior PV Associate at ICON plc
Application Link
Grow Your Career with ICON
By joining ICON plc as a Pharmacovigilance Associate, you become part of a dynamic team dedicated to healthcare advancements. This is not just a job—it’s a platform for career development, allowing you to contribute to meaningful projects that directly impact patient safety and health outcomes. ICON’s culture emphasizes continuous learning, global collaboration, and innovative problem-solving, making it an ideal place to develop your professional skills. Pharmacovigilance Associate/Senior PV Associate at ICON plc
Are you ready to be a part of ICON’s global mission? Apply today and make your mark in healthcare research!