This is an exciting opportunity to join ICON
Clinical Research Associate (CRA I, CRA II and/or Sr CRA)
You MUST have minimum 1 year of EXPERIENCE as a CLINICAL RESEARCH ASSOCIATE to be considered.
Would you like to work for ICON, the highest ranked Clinical Research Organization in the best large employers listing Forbes for the third year in 2019?
As a top five Clinical Research Organization in the world, we are looking to strengthen our Clinical Operations team in the US. As a CRA you will work independently and actively handle all necessary activities required for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation. You will be involved in the submission of protocol,
consent documents for ethics/IRB approval and assist in the preparation of regulatory submissions as requested.
You will be supported with manageable sites & protocols, a strong benefits package that includes a comprehensive health plan, retirement plans, competitive pay, vacation, and eligible for the annual performance bonus? Additionally, we have innovative technology and provide excellent training to ensure better outcomes.
You will possess:
- Minimum of 1 year of active independent field monitoring experience- all types of visits.
- Minimum 1 year of Oncology experience as a CRA
- Deep understanding of ICH GCP Compliance.
- Excellent time management and social skills
- Highly motivated with a phenomenal eye for detail.
- Ability to travel 65-75% of the month.
- Bachelor's degree in a life science or related discipline OR RN/LPN with 4 years related experience.
Benefits of working with ICON:
- Comprehensive benefits package including premium salary
- 401K with employer match
- Paid holidays
- Company cell phone and equipment
- Market leading PTO
- Culture of teamwork and collaboration
- People who motivate and face challenges together
- Innovative technology
- Per-Diem as per US Govt guidelines
We care about our people and your passion, as they are the key to our success and provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long-term career. In addition, you will have the opportunity to develop within your role and tackle further responsibilities or develop your skill set within other related departments of ICON.
ICON Plc is an equal opportunity employer. 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
Benefits of Working in ICON :
Other than working with a great team of smart and energetic people, we also offer a very competitive benefits package. This varies from country to country so a dedicated recruiter will discuss this with you at interview stage.
We care about our people as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career.
ICON is an equal opportunity employer, including disability/veteran, and committed to providing a workplace free of discrimination and harassment.
Muestra tus habilidades a la empresa, rellenar el formulario y deja un toque personal en la carta, ayudará el reclutador en la elección del candidato.
Senior Clinical Research Associate At ICON, it's our people that set us , our work is serious business. But that doesn't mean you can't have fun while you do it. With our vision to be the partner of c [...]
Q2 Solutions is a leading clinical trial laboratory services organization with end-to-end laboratory services and secure, enterprise-wide biospecimen and consent management solutions. With a relentles [...]
Clinical Research Associate Senior **Ref #:** 23735 **Employment type:** Permanent - Full-Time **Location:** Buenos Aires, Argentina - homebased **Posted:** 28-Aug-2020 **Description** Clinical Resear [...]
Currently we are hiring in FSP Lilly Argentina a Manager, Clinical Operations to work with a team of CRAs and/or Coordinating CRAs. In this crucial role within IQVIA you will lead and motivate a team [...]