Pharmacovigilance Associate

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

Please note this role requires two days per week on site. The purpose of the ICON Pharmacovigilance Associate is to perform a broad range of activities to manage adverse event collection, processing and reporting activities on behalf of the client Global Patient Safety Team.

Perform tasks within assigned functional area team, building proficiency to meet targets for delivery and client expectations. Demonstrated understanding of the documented processes and conventions applicable to scope of own assigned activities. Growing understanding of the legislative requirements for activities performed.

Delivers quality and compliance in line with documented procedures and expectations, including those in program performance measures. Able to take steps to avoid late reporting and non-compliance. Contribute to investigations for corrective and preventative action plans. Aware of importance of own role and able to define where it fits into the wider department organisation with awareness of up and downstream activities. Aware of the QPPV role and their responsibilities. Supports inspection readiness through own activities and aware of why audits/inspections are conducted. Aware of the departmental Business Continuity Plan and when it may be implemented. Tasks are determined by assigned functional area team and allocated on a rotational basis. All activities are performed in line with the client's documented processes and conventions.

• Receipt, triage, and initial data entry of Individual Case Safety Reports (ICSRs) from different receipt sources in line with documented processes and conventions.
• Expedited and Aggregate Safety Reporting to Ethics Bodies.
• Own partner relationships for collection of adverse event information (including Patient Support Programs (PSP), Market Research, Medical Information, Digital Media, Third Party Organisations (TPOs)).
• Maintain and update EMA master data repositories.

Professional competencies: Communicates clearly and effectively verbally and in written formats in a variety of settings. Demonstrated ability to prioritise workload and complete all deliverables by deadlines set. Escalates issues effectively and proposes potential solutions based on own experiences. Makes informed experienced based decisions, and has awareness of own remit of authority. Builds and maintains relationships within functional area team to work collaboratively. Demonstrated ability to receive and appropriately act upon feedback. Able to provide constructive feedback regarding processes and delivery. Adheres to confidentiality guidelines and expectations with an understanding of how to identify and protect company information.

Minimum Effective communication skills (written and verbal), fluent in English. Proficient in Microsoft Office suite. Knowledge of medical terminology. Excellent organisational and time management skills with proven ability to prioritise and manage multiple deliverables. Detail orientated. Effectively respond to requirements and requests.

Preferred: 1+ years relevant experience in Clinical industry. Knowledge of global regulations with respect to pharmacovigilance. Knowledge of medical coding systems. Ability to work autonomously, influencing without authority, ability to network ideas in corporate environment. Provide and apply constructive feedback to/from colleagues. Ability to learn quickly and adapt to a changing environment. Flexibility to adapt to changing priorities. Demonstrated interpersonal skills. Ability to see the big picture; use logic to solve problems.

Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development. At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.