Buenos Aires, Autonomous City of Buenos Aires, Argentina
80 days ago
Senior Clinical Research Associate (Contractor)

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 a temporary freelance Clinical Research Associate to work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. 

Responsibilities will include:

Training, mentoring and supervising study level responsibilities for Jr. CRAsPreparation, conduct, and reporting of selection, initiation, routine and closeout monitoring visitsDelivering training of investigators, site staff and project teamsWork with complex studies in Infectious Diseases and OncologyPerform CRF review, source document verification and query resolutionBe responsible for site communication and managementBe involved in site identification processContact for clinical investigators, vendors and support services in regard to study progressParticipate in feasibility researchPreparation and delivering of presentations at Investigator’s MeetingsPreparation for and attendance at company’s audits; resolution of audit findingsSupport to Regulatory Affairs in procurement of site regulatory documentsMaintenance of study-specific automated tracking systems

 

QualificationsCollege/University degree in Life Sciences or an equivalent combination of education, training & experienceFull working proficiency in Spanish and EnglishIndependent on-site monitoring experience in ArgentinaExperience in all types of monitoring visits in Phase II and/or IIIAvailability to travelExperience in Oncology or Infectious Diseases is a plusProficiency in MS Office applicationsAbility to plan and work in a dynamic team environmentCommunication, 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.

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