Job Description Take your career to the next level and be involved in study startup processes in Argentina.You will provide direct operational support to project teams and ensure that PSI clinical projects start smoothly and on time. Hybrid work You will: Oversee and coordinate the processes critical for clinical trial sites activation Communicate with project teams, investigative sites, review bodies, vendors, and clients regarding startup matters till the moment of site activation Support site identification and selection process Collect, review, and submit documents for ethics and regulatory review and approval Prepare packages of site documents for drug release to clinical sites Develop and negotiate site contracts and budgets Monitor startup metrics and timelines Coordinate initiatives for startup process improvement, analyze best practices and challenges Qualifications College/University degree or an equivalent combination of education, training and experience Minimum 3 years of industry experience in clinical research with practical startup experience in the Country/ Region Excellent knowledge of ICH GCP, local laws and applicable regulations in the region Full working proficiency in English and Spanish Communication and organizational skills Ability to negotiate and build relationships at all levels Experience in mentoring and leadership is preferred Additional Information What we offer: We value your time so the recruitment process is as quick as 3 on-line meetings We'll prepare you to do your job at highest quality level with our extensive onboarding and mentorship program You'll have permanent work agreement at a stable, privately owned company We care about our employees - aside from competitive salary, you'll have good work-life balance and attractive benefits We're constantly growing which means opportunities for personal and professional growth Please note: only CVs in English will be considered