Clinical Affairs Specialist

About the RoleWe are seeking a highly skilled Medical Education Specialist to join our Clinical Affairs team at Edwards Lifesciences. As part of this role, you will play a critical part in generating and disseminating evidence-based clinical practices that impact patient lives and advance the quality of care.

**About the Role:**Citi is seeking a Compliance Regulatory Affairs Specialist to support the design, development, delivery and maintenance of best-in-class Compliance programs, policies and practices for ICRM.**Responsibilities:**

About the RoleWe are seeking a highly skilled Regulatory Affairs Analyst to join our team in Sao Paulo, Brazil.The ideal candidate will have a strong understanding of international and local regulations on Clinical Trials, as well as excellent communication skills.Key ResponsibilitiesDevelop Informed Consent Forms and regulatory dossiers for initial...

Job Title: Senior Clinical Research SpecialistAbout the Company:ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.We are currently seeking a Clinical...

**Company Overview**We are Aspen Medical, a leading healthcare provider dedicated to delivering high-quality medical services in remote and challenging environments. Our team of experts works tirelessly to provide life-saving care to those in need.**Job Description**We are seeking an experienced Clinical Care Specialist to join our team. As a Clinical Care...

Job DescriptionWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Sewell Lincoln. This role will be responsible for coordinating and submitting new drug / medical devices applications to regulatory agencies in Brazil.Key Responsibilities:Plan, conduct and coordinate JJV regulatory activities for Brazil, ensuring compliance with...

Job DescriptionWe are seeking a skilled Clinical Trial Operations Specialist to lead our country-level operations in this exciting role. As a key member of our team, you will be responsible for providing local management services for clinical trials and medical affairs data generation activities.Responsibilities:Oversight of assigned projects at the country...

About ICON">ICON is a world-leading healthcare intelligence and clinical research organization. We foster an inclusive environment that drives innovation and excellence.We are committed to shaping the future of clinical development through our diverse and dynamic team.Job Summary">We are seeking a Clinical Research Associate II Specialist to join our team....

Company Overview:">Milestone One is a pioneering Site Enabling Organization headquartered in Zug, Switzerland. Our mission is to empower clinical study sites worldwide by providing unparalleled support and expertise.">Job Summary:">We are seeking an experienced Global Clinical Trial Liaison Specialist to join our dynamic team. In this role, you will be...

About the Role">This role is an exciting opportunity to utilize your clinical expertise in cardiovascular imaging to drive education and operational excellence within a specific modality or product portfolio.As a key member of our team, you will provide expert support to clinical end-users, leveraging your knowledge of relevant imaging equipment operation...

About the RoleWe are seeking a highly skilled North American Regulatory Affairs Specialist to join our team at Thermo Fisher Scientific. As a key member of our regulatory affairs team, you will be responsible for providing innovative regulatory solutions and expertise to support product development from preclinical stages through registration and product...

Company Overview:At ICON Plc, we are a world-leading healthcare intelligence and clinical research organization. Our mission is to shape the future of clinical development by fostering an inclusive environment that drives innovation and excellence.Salary:$80,000 - $110,000 per yearAbout the Role:We are seeking a highly skilled Clinical Safety Reporting...

Job DescriptionThe Clinical Study Execution Specialist supports the execution of clinical studies by collaborating with clinical research staff and project delivery teams to ensure timely completion of study tasks. This role is responsible for providing site workers with the necessary technical access, supplies, and administrative support to conduct required...

We are seeking a skilled Regulatory Affairs Analyst to join our team in São Paulo, Brazil. This role will be responsible for executing registration strategies for designated regional projects related to new and existing products, ensuring compliance with local regulations and approved licenses.The successful candidate will have a strong background in...

About UsBayer is a leading global company with core competencies in the areas of life sciences, healthcare, and agriculture. We are committed to making a positive impact on people's lives and improving their quality of life through our innovative products and services.Our Regulatory Science TeamWe are a team of talented and strategic regulatory science...

The Role:We are seeking an experienced Senior R&D Procurement Specialist to join our team at Organon. This position will play a key role in developing and executing a multi-year sourcing strategy that expands the capability and flexibility of working with external partners across the R&D organization.The ideal candidate will have a strong background in...

Company OverviewThermo Fisher Scientific is a leading global contract research organization (CRO) dedicated to improving health. Our Clinical Research team is at the forefront of getting cures to market, bringing high-caliber scientific and clinical expertise to the development of drugs addressing challenging health concerns.

About ICON plc">ICON plc is a world-leading healthcare intelligence and clinical research organization. We foster an inclusive environment driving innovation and excellence.">Job Overview">We are seeking a Clinical Research Associate II Specialist to join our diverse team. As a key member, you will contribute to the delivery of high-quality clinical research...

Site Activation Manager Role OverviewIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and...

Medpace is a dynamic and rapidly growing company with clinical trial activities increasing in South America. We are seeking a full-time, office-based Clinical Research Project Coordinator to join our Clinical Trial Management team. This position will be instrumental in accomplishing tasks and projects that drive the company's success.Responsibilities:•...