This job has expired

Drug Safety Associate

Employer
ICON GSS - EMEA
Location
United Kingdom
Salary
Competitive
Start date
21 Nov 2022
Closing date
29 Nov 2022

View more

Discipline
R & D , Pharmacology
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)
You need to sign in or create an account to save a job.

Job Details

Role: Drug Safety Associate

Location: Berkshire

Fully sponsor dedicated

ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations. With our patients at the center 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.

The purpose of the ICON Drug Safety Associate is to manage adverse event collection, processing and reporting activities, dedicated to a global pharmaceuticals client.

Delivery
  • 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.


Quality and compliance
  • 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 sponsor's documented processes and conventions. The following are considered core team tasks for each work stream; additional responsibilities may be assigned across the groups as appropriate and at the discretion of ICON and sponsor management.

Safety Management:
  • Handling and data entry of Individual Case Safety Reports (ICSRs) from different receipt sources and therapeutic areas.
  • Expedited Safety Reporting to Regulatory Authorities (EMA, MHRA, HPRA).
  • Provide operational support to Country Affiliates.


UK Affiliate, Operations Team:
  • 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
  • Displays integrity


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
  • 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.

Eductional requirements
  • Bachelor’s degree (or higher) in a healthcare-related or life science field
  • Demonstrated equivalent experience


Benefits of Working in ICON:

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, color, 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.

Company

ICON is the leading provider of Functional Service Provision (FSP) globally. Our team of operational, functional and therapeutic specialists offer a range of FSP models that can be customised to deliver the most efficient operating model for your organisation. We bring a suite of capabilities, expertise and technology to augment your operations, increase R&D efficiencies and improve site engagement to access patient populations and deliver timelines and milestones. We have deployed FSP solutions across all major functions from clinical monitoring and project management through data management, statistical programming and beyond.

 

ICON FSP experience

  • 90+ FSP partnerships
  • 13,000+ Employees
  • 90+ Countries

 

Functional areas

Our offering includes a range of globally scalable FSP solutions that are customised to provide support where and when you need it. We have significant experience in providing bespoke FSP solutions, particularly in:

  • Study start-up
  • Project Management
  • Clinical monitoring
  • Pharmacovigilance / Safety
  • Clinical Supplies Management
  • Data management

Biostatistics and programming

Contracts management

  • Investigator payments
  • Clinical vendor management & category management
  • Medical writing
  • Medical affairs
  • Regulatory affairs
  • Regulatory publishing
Find Us
Website
Location
500 South Oak Way
Green Park
Reading
Berkshire
RG2 6AD
GB
You need to sign in or create an account to save a job.

Get job alerts

Create a job alert and receive personalised job recommendations straight to your inbox.

Create alert