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DOCS Clinical Research Associate (CRA) *Home based in United States

Clinical Research Associate (CRA) *Home based

Ref #: 27044

Employment type: Permanent - Full-Time

Location: Buenos Aires

Description

Description:

  • Participates in site feasibility and/or pre-trial site assessment visits, providing recommendation from local area about site/investigator selection in collaboration with the trial team

•* Acts as primary local company contact for assigned sites for specific trials.

•* Attends/participates in investigator meetings as needed.

•* Responsible for executing activities within site initiation and start-up, site monitoring, site management and site/study close-out according to internal SOPs/WIs/IFUs and policies.

•* Ensures site staff is trained and the corresponding training records are complete and accurate at any time point during all trial phases.

•* Contributes to site level recruitment strategy and contingency planning and implementation in partnership with other functional areas to achieve clinical research target.

  • Ensures site study supplies (such as Non-IP, lab kits, etc.) are adequate for trial conduct.

•* Ensures that all AEs/SAEs/PQCs are reported within the required reporting timelines and documented as appropriate. For AEs/SAEs, ensures that they are consistent with all data collected and with the information in the source documents.

•* Maintains complete, accurate and timely data and essential documents in systems utilized for trial management (e.g. CTMS, eTMF/IF, Trial Master Source and Sharepoints).

Profile:

•* A minimum of a BA/BS degree is required. A degree in a health or science related field is preferred.

•* Must have experience in Clinical Research or equivalent qualification

•* Usually 0-2 years’ experience monitoring on site

•* Specific therapeutic area experience may be required depending on the position.

•* Strong working knowledge of ICH-GCP, company standard operating procedures, local laws and regulations, assigned protocols and associated protocol specific procedures including monitoring guidelines.

•* Strong IT skills in appropriate software and company systems. Willingness to travel with occasional overnight stay away from home.

•* Proficient in speaking and writing the country language and English.

•* Good written and oral communication skills.

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DOCS is an equal opportunity employer - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment.

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