
1001 - 5000 employees
Founded 1996
đĽ Healthcare
đź Consulting
đŚ Logistics
Healthcare ⢠Consulting ⢠Logistics
PSI CRO AG is a global contract research organization (CRO) that specializes in conducting clinical trials. The company focuses on delivering pivotal Phase 2 and 3 clinical trials across various therapeutic areas, including Inflammatory Bowel Diseases, Oncology, Hematology, Infectious Diseases, Multiple Sclerosis, and Rare Diseases. PSI utilizes a proprietary technology platform for clinical trial planning and financial tracking to ensure trials are conducted on time and within budget. The company is recognized for its expertise, quality, compatibility, and reliability, having been awarded the CRO Leadership Awards for multiple consecutive years.
đĽ 1 minute ago
đŚđˇ Argentina â Remote
â° Full Time
đ Senior
đ´ Lead
đ§Ş Clinical Research
đť Ghost score 10%
đŁď¸đŞđ¸ Spanish Required
Where this job comes from
Posted on PSI CRO AG's careers page, not through a job board
First seen by Remote Rocketship 1 minute ago

1001 - 5000 employees
Founded 1996
đĽ Healthcare
đź Consulting
đŚ Logistics
Healthcare ⢠Consulting ⢠Logistics
PSI CRO AG is a global contract research organization (CRO) that specializes in conducting clinical trials. The company focuses on delivering pivotal Phase 2 and 3 clinical trials across various therapeutic areas, including Inflammatory Bowel Diseases, Oncology, Hematology, Infectious Diseases, Multiple Sclerosis, and Rare Diseases. PSI utilizes a proprietary technology platform for clinical trial planning and financial tracking to ensure trials are conducted on time and within budget. The company is recognized for its expertise, quality, compatibility, and reliability, having been awarded the CRO Leadership Awards for multiple consecutive years.
⢠Act as the primary point of contact for trial-specific medical and safety-related questions ⢠Provide input for responses to regulatory authorities and Institutional Review Boards/Independent Ethics Committees ⢠Monitor trial participant safety ⢠Participate in participant recruitment boost and retention activities ⢠Present medical matters at kick-off and investigator meetings ⢠Train trial teams in the therapeutic area and protocol medical aspects ⢠Develop and review trial-specific documents within medical monitoring scope ⢠Manage ongoing trial risks related to medical monitoring ⢠Perform ongoing medical review of operational clinical trial databases ⢠Review protocol deviations, RAE reports, SAE narratives, safety queries, and IND/SUSAR Safety Reports ⢠Participate in trial-related committees, including independent data monitoring and adjudication committees ⢠Support Pharmacovigilance, Medical Data Review, and Data Management with safety and database reconciliation ⢠Review clinical study reports, including safety narratives and tables, figures, and listings ⢠Provide medical expertise on an as-needed basis ⢠Prepare for and participate in trial audits and follow up on audit findings ⢠Participate in feasibility assessments of potential and ongoing trials in the country/region ⢠Participate in bid defense meetings and client interactions ⢠Act as a medical expert and provide therapeutic expertise to other PSI departments
⢠Medical Doctor degree required ⢠Experience as a practicing Gastroenterologist (minimum of 10 years) ⢠Clinical Research experience preferred ⢠Full working proficiency in English and Spanish ⢠Proficiency with MS Office applications ⢠Communication, presentation and analytical skills ⢠Problem-solving, team and detail-oriented ⢠Ability to work from home in Argentina
⢠Employees can work remotely ⢠Full-time employment ⢠Opportunity to join an international group of medical professionals ⢠Career development on the frontline of medical science ⢠Opportunity to use medical expertise to help bring new medications to patients
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