Our Own It culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.
Thats our vision. Were driven by it. And we need talented people who share it.
If youre as driven as we are, join us. Youll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and youll be helping shape an industry.
Role:
Recognize, exemplify and adhere to ICON's values, which center on our commitment to People, Clients and Performance
- Ability to work on study teams that are often virtual, multi-cultural, and multi-disciplinary
- Serves as the primary contact for sites and investigators participating in studies
- Conducts and completes remote site management activities, with support as needed, according to applicable SOPs and the Site Management Plan
Our success depends on the quality of our people. Thats why weve made it a priority to build a culture that rewards high performance and nurtures talent.
- Participates in QA audits as needed
- Reviews drug storage and drug accountability procedures (as applicable), in accordance with applicable SOPs
- Assists with timely preparation and submission of regulatory documents for IRB/IEC submissions according to local requirements, with support, as needed
- Assumes additional responsibilities as detailed and documented by PM or delegate, RS Lead or Line Management
- Assists in development of site and patient enrolment strategies with project team; works to motivate sites to meet enrolment timelines
- Demonstrates ability to implement the study monitoring plans/metrics as appropriate and agreed upon
- Compliant and current with departmental and corporate policies and procedures
- A Clinical Trial Assistant / In-House CRA / Remote Site Monitor with experience including off site monitoring experience
- A CRA who no longer wants to travel
- A Study Coordinator or Study Nurse with good experience facilitating monitoring visits, collecting data, dealing with queries and running studies per ICH GCP guidelines who is interested in working for a CRO
- Scientific knowledge background an advantage
- Strong understanding of Regulatory requirements for South Africa and Local Submissions
- Team player with strong leadership & communication skills
- Fluent English and local language
- Ability to multi-task and prioritize to meet metrics and timelines
- Attention to detail and quality focus
- Ability to problem solve with sites and answer protocol questions
- Meets and embodies ICON Core Values
Our success depends on the quality of our people. Thats why weve made it a priority to build a culture that rewards high performance and nurtures talent.
We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans and related benefits such as life assurance so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, youll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.
ICON 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 through the form below.
