Senior Cra

Domino Data Lab; Buenos Aires; A distancia; USD 40.000 - 80.000; Jornada completa

Descripción de la vacante

A forward-thinking company seeks a Senior Clinical Research Associate (CRA) for a home-based role. This position involves coordinating and monitoring clinical studies, ensuring compliance with ICH GCP guidelines, and producing accurate work under tight deadlines. Ideal candidates will have over 18 months of experience in phase I-III trials and possess excellent communication skills. Join a team that values continuous learning and offers a competitive total reward package, including comprehensive benefits and opportunities for professional development. This is a chance to make a significant impact in the healthcare industry.

Formación

• 18 months+ of monitoring experience as a CRA.
• Knowledge of ICH GCP guidelines and medical data evaluation.

Responsabilidades

• Coordinate activities to set up and monitor clinical studies.
• Assist in preparing regulatory submissions and study documentation.

Conocimientos

Monitoring experience in phase I-III trials

Knowledge of ICH GCP guidelines

Excellent written communication skills

Excellent verbal communication skills

Ability to work under pressure

Willingness to travel

Descripción del empleo

Sr CRA - Home-based role

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 Role

1. Working independently and actively to coordinate activities to set up and monitor a study, completing accurate study status reports and maintaining study documentation.
2. Submission of protocol, consent documents for ethics/IRB approval and assist in preparing regulatory submissions as requested.
3. Participate in preparing and reviewing study documentation and feasibility studies for new proposals as required.
4. Balancing sponsor-generated queries efficiently and responsible for study cost-effectiveness.
5. Depending on level of experience, you may assist in training and mentoring less experienced CRAs and/or lead CRAs working on international projects.

What you need

1. 18 months+ of monitoring experience in phase I-III trials as a CRA.
2. Knowledge of ICH GCP guidelines and expertise to review and evaluate medical data.
3. Excellent written and verbal communication skills in English.
4. Ability to produce accurate work to tight deadlines within a pressurized environment.
5. Willingness to travel at least 60% of the time.

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 includes an excellent base pay, a wide range of variable pay and recognition programs, and best-in-class employee benefits, supportive policies, and wellbeing initiatives 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 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.