Senior Clinical Research Associate at PSI CRO

São Paulo, São Paulo, Brazil -

Full Time

Start Date

Immediate

Expiry Date

18 Mar, 26

Salary

0.0

Posted On

18 Dec, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research, Training, Mentoring, Monitoring, Oncology, Infectious Diseases, Communication, Collaboration, Problem-Solving, MS Office, Site Management, Feasibility Research, Regulatory Affairs, Presentation Skills, Source Document Verification, Query Resolution

Industry

Pharmaceutical Manufacturing

Description

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 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 develop 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 Portuguese and English Independent on-site monitoring experience in Brazil 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 rapid growing company that puts its people first.

Responsibilities

The Senior Clinical Research Associate will train, mentor, and supervise junior CRAs while conducting monitoring visits and managing site communications. They will also be involved in site identification and support regulatory affairs.