Applicable Regulations Jobs in Argentina

Job OverviewReview assess and process safety data and information across service lines received from various sources. Distribute reports/data to both internal and external third parties following applicable regulations Standard Operating Procedures (SOPs) and internal guidelines under the guidance a...

Site Activation Coordinator Job OverviewUnder general supervision perform tasks at a country level associated with site activation activities in accordance with applicable local and/or international regulations standard operating procedures (SOPs) project requirements and contractual/budgetary guide...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Clinical Trial Coordinator Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700 clinical trials across 100 cou...

Job Overview:Primary contact with investigative sites during study maintenance and -when assigned- site startup activities with responsibility for collection of the required investigator and regulatory essential documents to ensure EC/IRB/Third body/Regulatory Authority submissions are made within t...

When our values align theres no limit to what we can achieve.At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a deep conviction in...

This role is ideal if youre looking to start your career in pharmacovigilance its not required that you have experience in the field but it will be a plus!Fixed-term role for 6 monthsFull-time position Monday to FridayWork modality: Home-basedMay require working on ARG national holidaysJob OverviewR...

This role is ideal if youre looking to start your career in pharmacovigilance its not required that you have experience in the field but it will be a plus!Fixed-term role for 6 monthsEnglish and Portuguese advanced mandatory will be evaluated with assessment. We wont consider profiles with less than...

Job OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations standard operating procedures (SOPs) project requirements and contractual/budgetary guidelines. May also include maintenance activities.Es...

Job OverviewManage a team of clinical staff working in support of clinical studies to ensure projects are appropriately resourced and employees are trained and meeting project objectives.Essential Functions Manage staff in accordance with organizations policies and applicable regulations. Responsibi...

Clinical Trial Manager Sponsor Dedicated.Clinical Project Management services provide management of a clinical trial (s) in a local level. Services/deliverables include operational oversight of assigned project(s) at country level for end-to-end project management from start-up through to closeout...

is connecting the world to the future of finance. As the most trusted and fastest-growing global crypto company it helps millions of people worldwide safely access cryptocurrency. Since its inception in 2011 has earned the trust of over 90 million wallet holders and more than 40 million verified u...

Senior Site Activation CoordinatorHybrid- ArgentinaMake an impact on patient health!IQVIAs Global Site Activation Team of 2000 employees drives best in class site and customer experience with industry leading outcomes.We keep the patient at the forefront; Always Impatient for the Patient and we exce...

Senior Site Activation CoordinatorHybrid - Buenos Aires ArgentinaMake an impact on patient health!IQVIAs Global Site Activation Team of 2000 employees drives best in class site and customer experience with industry leading outcomes.We keep the patient at the forefront; Always Impatient for the Patie...

Job Overview:Primary contact with investigative sites during study maintenance and -when assigned- site startup activities with responsibility for collection of the required investigator and regulatory essential documents to ensure EC/IRB/Third body/Regulatory Authority submissions are made within t...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJob DescriptionQualifications:EducationandExperience:Bachelors degree in a life science difficulty or related field or a Registered Nursing certification orequivalent and relevant formal academic / vocational qualification.P...

We help the world run betterAt SAP we keep it simple: you bring your best to us and well bring out the best in you. Were builders touching over 20 industries and 80% of global commerce and we need your unique talents to help shape whats next. The work is challenging but it matters. Youll find a pla...

Work ScheduleEnvironmental ConditionsJob DescriptionSummarized Purpose:Performs remote activities on assigned projects in liaison with the CRA and study Clinical Lead. Providessupport with regards to site preparedness logistical support to the monitoring process and assist withassigned tasks for sit...