Pharmacovigilance Analyst (R1109479)

Job Description

IQVIATM is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.

Pharmacovigilance (PV) Analyst - (PRIMARY INTELLIGENCE)

IQVIA has been delivering primary market research (PMR) services to the healthcare industry for over 15 years. Since 2014, IQVIA consolidated its go-to-market and delivery approach for its PMR services and formed an independent practice – Primary Intelligence. PI focuses on providing clients with a holistic solution to its research needs, by combining its primary research practices along with IQVIA’s extensive data assets PI can gives unique insights into the life sciences industry. We provide our services in 50+ countries, in 20+ languages and have a global community of 500+ expert PMR professionals as part of our PI organization within IQVIA.

You’ll be truly part of a global community, have opportunity to work with a diverse range of cultures and hone your skills on global client projects. You’ll gain exposure to various primary research techniques and patented methodologies, state-of-the-art tool sets, pioneering data assets across numerous therapy areas and be part of one of the vibrant and fast growing IQVIA businesses.

Our hub in Prague is looking for a Pharmacovigilance (PV) Analyst. The PV Analyst will report to the PV Manager and acts as a link between Project Manager, Legal, field/Quality Control teams and the end client to ensure that IQVIA fulfils regulatory and contractual pharmacovigilance requirements.

Responsibilities will include:

• Negotiating contractual terms with clients
• Identifying PV risks including off-label uses of client products
• Liaising with client contacts and internal colleagues to manage training and reporting requirements
• Monitoring and reporting safety data
• Conducting quality checks and source data verification
• Providing guidance to colleagues on PV matters
• Reconciliation preparation
• CAPA creation and follow-up
• Handling client queries and follow-up of cases

Desired Skills and Experience

• Native or fluent English is essential
• Good communication skills appropriate to a global working environment and communication with senior internal and client personnel
• Familiarity with PV requirements and PMR is a distinct advantage
• Familiarity with Quality Management Systems and CAPA management
• Experience in contract negotiations
• Works willingly and effectively with others in and across the organization to accomplish project goals
• Disciplined, self-motivated and able to operate effectively as part of a team
• Ability to work to deadlines, as well as constant prioritisation of work
• Effective time management skills
• Ability to multi-task is vital
• Good time management and organizational skills
• A strong motivation to thrive in a client-focused, international team environment
• Willingness to be flexible in working hours
• Eligible to work in Czech Republic without visa sponsorship

In addition to the skills and experience above, candidates interested in joining IQVIA will have:

• Bachelor’s degree with min. 1 - 3 years of experience
• A strong commitment to high quality work and an interest in rapid learning and skill development.

Join Us

Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.

Forge a career with greater purpose, make an impact, and never stop learning.