â weâre able to create a place where everyone feels like they belong. Job Responsibilities May lead multi-country... clinical trials. Produces site-specific contracts from country clinical trial agreement (CTA) template. Reviews and owns site...
A leading clinical research company in Buenos Aires seeks a Lead Data Manager to oversee data management activities...
Job Overview The Leader of the Centralized Monitoring team, partner with the project and clinical lead to achieve the...: Leader of the Centralized Monitoring team, partner with the project and clinical lead to perform oversight on clinical...
, timeliness and completeness. Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator... face to face meetings. Participates, and may, with supervision, lead, global clinical monitoring/project staff meetings...
, timeliness and completeness. Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator... face to face meetings. Participates, and may, with supervision, lead, global clinical monitoring/project staff meetings...
, timeliness and completeness. Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator... face to face meetings. Participates, and may, with supervision, lead, global clinical monitoring/project staff meetings...
, and operational oversight for clinical trial business operations and feasibility management at the country/regional level. Ensures... clinical development and business opportunities.Lead country and regional feasibility assessments, ensuring alignment...
of the ISF with the Trial Master File (TMF). Ensures the investigator/physician site is aware of the requirement of archiving..., with supervision, lead, integral clinical monitoring/project staff meetings (inclusive of Sponsor representation, as applicable...
, timeliness and completeness. Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator... face to face meetings. Participates, and may, with supervision, lead, global clinical monitoring/project staff meetings...
funnel by driving a strategic roadmap and experiments — from landing page experience through trial and onboarding. This role... experiences - Lead the Funnel Design and Engineering squad to rapidly ship and iterate on improvements - Work closely...
documents repository. Lead SPVG Regulatory Intelligence's Impact Assessment for assigned RI Item, coordinate input... trial process across Phases II-IV and post-marketing safety requirements, ICH GCP, GVP and regulations related to Safety...
-specific CDS documents in the Trial Master File (TMF) are of high quality and are filed contemporaneously to support downstream... Lead, Clinical Data Sciences, Clinical Data Sciences. Supports Study and Asset Teams across Research and Development. EEO...
and completeness. Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator/physician site is aware..., with supervision, lead, general clinical monitoring/project staff meetings (inclusive of Sponsor representation, as applicable...
of the ISF with the Trial Master File (TMF). Ensures the investigator/physician site is aware of the requirement of archiving..., with supervision, lead, general clinical monitoring/project staff meetings (inclusive of Sponsor representation, as applicable...
, timeliness and completeness. Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator... face to face meetings. Participates, and may, with supervision, lead, global clinical monitoring/project staff meetings...
, timeliness and completeness. Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator... face to face meetings. Participates, and may, with supervision, lead, global clinical monitoring/project staff meetings...
and local vendors, including FSP services. Implement outsourcing strategies aligned with global trial oversight deliverables.... Execute vendor management strategy locally, covering operational delivery, quality, contracts, and financial oversight. Lead...
documents repository. - Lead SPVG Regulatory Intelligence’s Impact Assessment for assigned RI Item, coordinate input... understanding of clinical trial process across Phases II-IV and post-marketing safety requirements, ICH GCP, GVP and regulations...
, timeliness and completeness. Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator... face to face meetings. Participates, and may, with supervision, lead, global clinical monitoring/project staff meetings...
-specific CDS documents in the Trial Master File (TMF) are of high quality and are filed contemporaneously to support downstream... OR ENVIRONMENT REQUIREMENTS Ability to travel ~5%. ORGANIZATIONAL RELATIONSHIPS Reporting relationship to Senior Manager, Asset Lead...