Experienced Clinical Safety Coordinator
hace 2 semanas
Our Latin American activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Safety Coordinator to join our team This position plays a key role in the pharmacovigilance process at Medpace. Working in a team to accomplish tasks and projects that are instrumental to the company's success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.
Responsibilities- Oversight of submission of safety reports in the appropriate format to Competent Authorities/Ethics Committees in compliance with regulatory timelines;
- Regular interaction with other internal departments globally and locally, such as Clinical Operations, Data Management, and Regulatory Submissions;
- Draft study specific safety documents as required;
- Work in a global team to distribute safety reports globally.
- Bachelor's degree in life science area is required;
- Demonstrate fundamental knowledge of Good Clinical Practice (GCP) guidelines and medical terminology;
- Knowledge of Electronic Data Capture (EDC) systems and other clinical databases;
- Experience safety reporting to regulatory authorities in Spanish speaking LATAM countries;
- Drug safety experience;
- Knowledge of applicable safety reporting guidelines;
- Strong attention to detail;
- 3 years of experience of working within drug safety;
- Fluency in Spanish & English.
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral, and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.
Why Medpace?People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
Medpace Perks
- Flexible work environment
- Competitive compensation and benefits package
- Competitive PTO packages
- Structured career paths with opportunities for professional growth
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
Awards
- Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023, and 2024
- Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility.
What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
EO/AA Employer M/F/Disability/Vets
#J-18808-Ljbffr-
Clinical Safety Coordinator Specialist
hace 4 minutos
Buenos Aires, Buenos Aires C.F., Argentina Medpace, Inc. A tiempo completoJob OverviewWe are seeking a full-time Clinical Safety Coordinator to support our growing Latin American activities. This role plays a key part in the pharmacovigilance process at Medpace.Key ResponsibilitiesSubmission of safety reports to regulatory authorities in compliance with timelines;Interaction with internal departments globally, including Clinical...
-
Safety Reporting Expert
hace 4 minutos
Buenos Aires, Buenos Aires C.F., Argentina Medpace, Inc. A tiempo completoJob ProfileWe seek an experienced Clinical Safety Coordinator to join our team in Latin America. This role involves working closely with internal stakeholders, ensuring compliance with regulatory requirements, and developing safety documents for studies.Main TasksPreparing and submitting safety reports;Collaborating with cross-functional teams;Ensuring...
-
Clinical Research Coordinator
hace 6 días
Buenos Aires, Buenos Aires C.F., Argentina IQVIA A tiempo completoCompany OverviewIQVIA is a leading provider of healthcare consulting and technology solutions. We are dedicated to helping our clients navigate the complexities of clinical research and improve patient outcomes.Job DescriptionClinical Research CoordinatorWe are seeking an experienced Clinical Research Coordinator to join our team in Quilmes centro, Provincia...
-
Medical Safety Analyst
hace 4 minutos
Buenos Aires, Buenos Aires C.F., Argentina Medpace, Inc. A tiempo completoRole DescriptionThis position requires a skilled Clinical Safety Coordinator to support our expanding presence in Latin America. You will be responsible for ensuring compliance with regulatory requirements, collaborating with internal teams, and developing safety documents for studies.Key QualificationsBachelor's degree in a life science area;Familiarity...
-
Global Clinical Trials Coordinator
hace 4 días
Buenos Aires, Buenos Aires C.F., Argentina Innovaderm Research Inc. A tiempo completoAbout the RoleInnovaderm Research Inc. is seeking an experienced Global Clinical Trials Coordinator to join our team.The successful candidate will have a strong background in clinical trial coordination, with experience in managing multiple clinical trials simultaneously. This role is perfect for a highly organized and detail-oriented individual who is...
-
Clinical Payments Coordinator
hace 2 días
Buenos Aires, Buenos Aires C.F., Argentina Cielo Talent A tiempo completoAbout the Role: As a Clinical Payments Coordinator, you will contribute to the success of our Payment Office by ensuring accuracy and timeliness of site payments. You will work closely with internal and external teams to resolve issues and authorize study setups.
-
Clinical Research Coordinator
hace 4 días
Buenos Aires, Buenos Aires C.F., Argentina Psi Cro Ag A tiempo completoJob DescriptionWe are Psi Cro Ag, a dynamic and global company that brings together passionate individuals to work on the frontline of medical science. We care about our staff, clients, partners, and the quality of work we do.The Clinical Research Coordinator will be the key support to clinical research projects, streamlining communication, maintaining...
-
Medical Research Coordinator
hace 2 días
Buenos Aires, Buenos Aires C.F., Argentina Cabify A tiempo completoCabify is seeking a highly motivated and organized Medical Research Coordinator to join our diverse and dynamic team. As a Medical Research Coordinator, you will be responsible for coordinating and conducting clinical trials, ensuring that all trials are conducted with the highest level of integrity and adhere to regulatory requirements.Job...
-
Global Clinical Logistics Coordinator
hace 6 días
Buenos Aires, Buenos Aires C.F., Argentina Ventura TRAVEL A tiempo completoJob Description:The Global Clinical Logistics Coordinator will be responsible for managing global clinical supplies for multiple projects simultaneously. This includes coordinating and managing complex studies, handling client consultations, and serving as the primary point of contact between clients, project teams, vendors, and study...
-
Clinical Research Project Coordinator
hace 4 días
Buenos Aires, Buenos Aires C.F., Argentina Milestone One A tiempo completoAbout Psi CroPsi Cro is an international clinical research organization dedicated to supporting various projects worldwide.Job SummaryWe are seeking a highly skilled Clinical Research Project Coordinator to join our team in site management. As the main point of contact between site personnel and CRA, you will be responsible for ensuring seamless...
-
Clinical Trials Coordinator
hace 4 días
Buenos Aires, Buenos Aires C.F., Argentina Mondelēz International A tiempo completoWe are seeking a Clinical Trials Coordinator to join our team. As a key member of our regulatory compliance team, you will be responsible for coordinating clinical trials and ensuring compliance with regulatory requirements. You will work closely with divisional teams to provide consultative and tactical support, serving as a liaison for all individuals...
-
Clinical Trials Coordinator
hace 5 días
Buenos Aires, Buenos Aires C.F., Argentina ThermoFisher Scientific A tiempo completoAbout the RoleThis is an exciting opportunity to join Thermo Fisher Scientific as a Clinical Trials Coordinator. In this role, you will be responsible for coordinating and delivering multiple complex projects from initiation through delivery.The successful candidate will have a minimum of 2 years of experience in innovative project management, with expertise...
-
Clinical Trials Coordinator
hace 5 días
Buenos Aires, Buenos Aires C.F., Argentina IQVIA LLC A tiempo completoA successful Pharmacovigilance Specialist will possess excellent analytical, communication, and problem-solving skills to navigate complex regulatory requirements and ensure seamless collaboration with cross-functional teams.ResponsibilitiesAccurately process and analyze safety data to identify potential trends or patterns.Collaborate with healthcare...
-
Global Clinical Supply Chain Coordinator
hace 7 días
Buenos Aires, Buenos Aires C.F., Argentina Virtualmind A tiempo completoJob Summary:We are seeking an experienced Senior Project Manager for Clinical Research to lead our Global Clinical Supplies team. In this role, you will be responsible for overseeing the entire clinical supplies lifecycle, including purchasing, global inventory management, distribution, and destruction. You will also manage complex studies requiring primary...
-
Advertising Operations Coordinator
hace 6 días
Buenos Aires, Buenos Aires C.F., Argentina Syneos Health Clinical A tiempo completoSyneos Health Clinical is seeking an Advertising Operations Coordinator to support our digital marketing efforts. In this role, you will be responsible for setting up, optimizing, and growing search and social media advertising campaigns.Responsibilities:Set up and manage advertising campaigns across various platformsMonitor campaign performance and make...
-
Senior Project Manager for Clinical Research
hace 7 días
Buenos Aires, Buenos Aires C.F., Argentina Virtualmind A tiempo completoOverview:We are seeking a highly skilled Global Clinical Supply Chain Coordinator to join our team. In this role, you will be responsible for coordinating global clinical supplies lifecycle for assigned projects, including managing complex studies requiring primary and/or secondary packaging and labeling design, drug projections, distribution, returns,...
-
Clinical Development Expert
hace 6 días
Buenos Aires, Buenos Aires C.F., Argentina Psi Cro A tiempo completoJob OverviewPSI Cro seeks a seasoned Medical Monitor to provide critical medical input to global clinical studies. This role involves advising clients, project teams, and regulatory agencies on medical matters while ensuring the safety and well-being of study participants.Key Responsibilities:Collaborate with internal departments in preparing clinical...
-
Clinical Research Associate
hace 3 días
Buenos Aires, Buenos Aires C.F., Argentina Allergan A tiempo completoAs a Clinical Research Associate at Allergan, you will play a crucial role in advancing our pipeline by striving for excellence in clinical research. You will leverage new advanced capabilities to drive industry leading performance and partner with study teams, AbbVie internal R&D stakeholders, investigators, and site staff for meaningful and effective...
-
Site Clinical Trials Manager
hace 3 días
Buenos Aires, Buenos Aires C.F., Argentina Allergan A tiempo completoWe are seeking a highly skilled and motivated Clinical Research Associate to join our team at Allergan. As a Clinical Research Associate, you will be responsible for advancing our pipeline by striving for excellence in clinical research and leveraging new advanced capabilities to drive industry leading performance.Responsibilities:You will partner with study...
-
Oncology Clinical Advisor
hace 4 días
Buenos Aires, Buenos Aires C.F., Argentina Psi Cro A tiempo completoWe're seeking a skilled Oncology Clinical Advisor to join our team at PSI Cro. In this role, you'll provide medical input to global clinical studies and advise teams and business partners on key matters.Main Tasks:Collaborate with internal departments to prepare clinical development plans, protocols, investigator brochures, and other documents.Review and...