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CRA II

Employer
ICON Strategic Solutions
Location
Israel, Homeworking
Salary
Competitive
Start date
21 Mar 2023
Closing date
19 Apr 2023

View more

Discipline
Clinical Research, Clinical Operations
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details

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.

The Clinical Research Associate (CRA) acts as site manager between site staff and Pharmaceutical Company, working within local Affiliate supporting one or more clinical trial(s) in a development programme. CRA is responsible for tangible trial operational targets (KPIs) and ensuring the highest possible data quality in clinical trial(s). The position is home-based in Israel, reports to CRA Team Manager and will require travelling up to 60% of the time.

  • The primary point of contact between site staff and Client
  • Leadership of site management for the selection and initiation of sites as well as conduct and closing activities of the appointed studies in compliance with local regulations, ICH-GCP, Client procedures and protocol requirements to ensure data quality and study subject protection
  • Managing the site to meet patient recruitment rate and target
  • Delivery of results that have direct impact on the successful completion of the clinical programme
  • Communication about progress and critical issues that may impair trial progress to Regional Trial Manager (RTM)

  • Bachelor or master degree in Life Sciences or equivalent
  • Experience as CRA in the pharmaceutical industry or Clinical Research Organisation (CRO), min. 1 years
  • Ability to build and maintain relationships with sites
  • High focus on delivery and quality
  • Excellent communication and negotiation skills
  • High degree of trustworthines s
  • Adequate English verbal and writing skills, e.g. enabling understanding of the protocol and study documents as well as writing monitoring reports
  • IT proficiency
  • Proven decision making and problem solving capabilities
  • Ability to manage multiple priorities
  • Team oriented personality with high degree of flexibility
  • Ability and willingness to adjust quickly to new situations in a continuously developing environment
  • Act as an ambassador of the company
  • Flexibility is very important due to the large number of minor and major tasks coming from different customers


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

As the largest global provider of Functional Service Provision (FSP) with over 90 partnerships and 14,000+ employees, we have deployed FSP solutions across all major functions, from clinical monitoring and project management through data management, statistical programming, and beyond.

ICON Strategic Solutions teams are embedded in our clients' businesses, working as a dedicated resource within some of the world’s leading Pharmaceutical & Biotech companies. You will play a key role in helping to deliver cutting-edge research, working on novel therapies that deliver real impact.

Why choose a career with ICON Strategic Solutions?

Meaningful Work: You’ll contribute to cutting-edge projects that have a real impact on global healthcare. Your work will play a pivotal role in shaping the future of medicine and improving patient lives.

Collaborative Environment: We foster a collaborative and inclusive work culture that thrives on teamwork, diversity, and knowledge sharing. You'll have the opportunity to collaborate with industry-leading experts, learning from their experiences and growing both professionally and personally.

Innovative Technologies: At ICON Strategic Solutions, we embrace the latest technologies and tools to enhance our capabilities. You'll have access to state-of-the-art software and resources, empowering you to deliver high-quality results efficiently.

Career Growth: We value our employees and invest in their professional development. You'll have access to comprehensive training programs, mentorship opportunities, and a clear career progression path. We believe in recognizing and rewarding exceptional performance, providing ample scope for advancement within the organization.

Global Reach: Joining ICON Strategic Solutions means being part of a truly global company. With service capabilities in 92 countries, you'll have the chance to collaborate with colleagues from diverse backgrounds and gain exposure to projects with a global reach.

Company info
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