Clinical Research Associate

Psi CRO; São Paulo; Vor Ort; BRL 329.000 - 493.000; Vollzeit

Zusammenfassung

Psi CRO in Mexico is seeking a skilled Clinical Research Associate to join a growing team and develop into a senior, trainer, mentor, and leader.

You will conduct and report monitoring visits, train investigators and site staff, work with complex studies, and support regulatory activities. The position offers opportunities for career development and travel.

Qualifikationen

• Bachelor's degree in Life Sciences.
• At least 2 years in patient care or clinical environment.
• Full working proficiency in English.
• Willingness to travel.

Aufgaben

• Coordinate monitoring visits and report findings.
• Deliver investigator and site staff training.
• Support site qualification and feasibility activities.
• Assist in audits and regulatory document procurement.

Kenntnisse

Communication skills

Teamwork

English proficiency

Problem-solving

Training/mentoring ability

Ausbildung

Bachelor's degree in Life Sciences

Tools

MS Office

CTMS

Jobbeschreibung

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

Only CV's in English will be considered

We are looking for a CRA to join our team in Mexico. Here you will have the opportunity to develop yourself as a senior, trainer, mentor and leader. We are committed to develop our employees in their careers by providing tailored courses and mentoring.

Responsibilities will include:

• 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;
• At least2 yearsexperience in patient careand/or health care or clinical environment
• Full working proficiency in English
• Experience in Clinical Research is a plus
• Availability to travel
• 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 rapid growing company that puts its people first.