Senior Clinical Research Associate

PSI CRO; Buenos Aires; A distancia; USD 30.000 - 70.000; Jornada completa

Descripción de la vacante

An established industry player is seeking an experienced Clinical Research Associate (CRA) to mentor and train junior staff while managing complex studies. This home-based role offers an exciting opportunity to advance your career in clinical research, with a focus on training and supporting others. You'll be involved in various responsibilities, including conducting monitoring visits, preparing for audits, and collaborating with clinical investigators. Join a dynamic team committed to developing your skills and providing tailored courses to enhance your career in a rapidly growing company that prioritizes its employees.

Formación

• Full working proficiency in Spanish and English is required.
• Independent on-site monitoring experience in Argentina is essential.

Responsabilidades

• Train, mentor, and supervise junior CRAs on site.
• Conduct and report monitoring visits and site communications.
• Participate in feasibility research and prepare for audits.

Conocimientos

Monitoring Experience

Training and Mentoring

Communication Skills

Problem-Solving Skills

Collaboration Skills

Educación

College/University degree in Life Sciences

Herramientas

MS Office

Descripción del empleo

Company Description

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,500 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Job Description

Home-based position in Argentina
Only CV's in English will be considered

We are looking for an experienced CRA ready to train and coordinate junior CRAs on site. Here you will have the opportunity to develop yourself as a trainer, mentor and leader. We are committed to developing our employees in their careers by providing tailored courses and mentoring.

Responsibilities will include:

• Training, mentoring and supervising study level responsibilities for Jr. CRAs
• Preparation, conduct, and reporting of selection, initiation, routine and closeout monitoring visits
• Delivering training of investigators, site staff and project teams
• Work with complex studies
• Perform CRF review, source document verification and query resolution
• Be responsible for site communication and management
• Be involved in site identification process
• Contact for clinical investigators, vendors and support services in regard to study progress
• Participate in feasibility research
• Preparation and delivering of presentations at Investigator’s Meetings
• Preparation for and attendance at company’s audits; resolution of audit findings
• Support to Regulatory Affairs in procurement of site regulatory documents
• Maintenance of study-specific automated tracking systems

Qualifications

• College/University degree in Life Sciences or an equivalent combination of education, training & experience
• Full working proficiency in Spanish and English
• Independent on-site monitoring experience in Argentina
• Experience in all types of monitoring visits in Phase II and/or III
• Availability to travel
• Experience in Oncology or Infectious Diseases is a plus
• Proficiency in MS Office applications
• Ability to plan and work in a dynamic team environment
• Communication, collaboration, and problem-solving skills

Additional Information

If you like to train and support others on their clinical research steps, and are also looking forward to future Lead Monitor roles, this position may just be the right one for you.
Advance your career in clinical research, coordinating a variety of tasks and learning new things while growing with a rapidly growing company that puts its people first.