Country Start Up Specialist

Study Start Up Associate II - Hybrid - Brazil 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 Study Start Up Associate...

Provides, under guidance local regulatory strategy advice (MoH &/or EC) to internal clients. - Provides project specific local SIA services and coordination of these projects. - May have contact with investigators for submission related activities. - Key-contact at country level for either Ethical or Regulatory submission-related activities. - Coordinates,...

Job Summary: As a Regulatory Submissions Coordinator you will have the opportunity to work within Regulatory Submissions, supporting our many projects and gaining some vital experience. You will be a productive member of the team, and will be mentored and supported as you develop your skills. Working directly with Regulatory Submissions Coordinators, you...

**Work Schedule** Other **Environmental Conditions** Office - Provides, under guidance local regulatory strategy advice (MoH &/or EC) to internal clients. - Provides project specific local SIA services and coordination of these projects. - May have contact with investigators for submission related activities. - Key-contact at country level for either...

Company Overview: BeiGene, Ltd. (NASDAQ: BGNE; HKEX: 06160) is a global, commercial-stage, research-based biotechnology company focused on molecularly targeted and immuno-oncology cancer therapeutics. With a team of over 10,000 employees across China, the United States (Cambridge, MA; Ridgefield Park, NJ; Emeryville, CA & San Mateo, CA), Switzerland,...

Job Summary As a Regulatory Submissions Coordinator you will have the opportunity to work within Regulatory Submissions, supporting our many projects and gaining vital experience in study start up. You will be a productive member of the team, and will be mentored and supported as you develop your skills. Working directly with Regulatory Submissions...

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development...

SSU responsibilities: - Coordinate guide and assist with all start up activities prior to site activation, including but not limited to: - Site Informed Consent Form (ICF) localization and guidance in line with regulatory/health authority requirements. - Ethics Committee information, meeting dates & costs. - Ethics & Governance submission processes. -...

Job SummaryOur LATAM clinical trial activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Study Start Up team in Sao Paulo. This position plays a key role in the clinical trial management process at Medpace. If you want an exciting career where you use your previous expertise and can...

Our LATAM clinical trial activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Study Start Up team in Sao Paulo. This position plays a key role in the clinical trial management process at Medpace. If you want an exciting career where you use your previous expertise and can develop...

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...

Job Summary: As a Regulatory Submissions Coordinator you will have the opportunity to work within Regulatory Submissions, supporting our many projects and gaining vital experience in study start up. You will be a productive member of the team, and will be mentored and supported as you develop your skills. Working directly with Regulatory Submissions...

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfill our mission to advance and improve patients' lives. ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research by providing...

Country Operations Specialist(Job Number: BRA0011) **Description** JOB DETAILS Department: Field Operations Job Title: Country Operations Specialist Reports To (title): Regional Operations Manager Career Level: 3 Location: Multiple Line Management Responsibility: Extended Workforce point of contact Job Purpose: Not limited to but including: -...

**Office**: São Paulo **Team**: Finance **Country Risk Specialist**: Wise is looking for a capable and enthusiastic Country Risk Specialist to join our team in São Paulo. The Country Risk Specialist will report directly to the country CRO, providing support and second line risk management advice and oversight to the specific entity and other countries in...

**Country Risk Specialist**: Wise is looking for a capable and enthusiastic Country Risk Specialist to join our team in São Paulo. The Country Risk Specialist will report directly to the country CRO, providing support and second line risk management advice and oversight to the specific entity and other countries in the Latin America region. Wise has...

**Country Risk Specialist**: Wise is looking for a capable and enthusiastic Country Risk Specialist to join our team in São Paulo. The Country Risk Specialist will report directly to the country CRO, providing support and second line risk management advice and oversight to the specific entity and other countries in the Latin America region. Wise has...

PLEASE SUBMIT ALL RESUMES/CV'S IN ENGLISH FOR CONSIDERATION Language Requirement: Fluent English and Portuguese. Spanish is a plus. Preferred Experience: Pharmaceutical/Biotech Industry, Hematology, Oncology General Description: - Supports the Regional Clinical Study Manager in regional study delivery and ensures that delegated components of clinical...

**PPD, now Thermo Fisher’s clinical research business, is a leading global contract research organization providing comprehensive, integrated drug development, laboratory, and lifecycle management services.** **At PPD, we are passionate, deliberate, and driven by our purpose - to improve health!** We are vital links between an idea for a new medicine and...

General Summary:The Field Service Specialist will assist customers with installation, start-up, calibration, training, troubleshooting and technical information for BTG products in the pulp and paper industry. This role will have close customer relationships that will range from E/I supervisors, process engineers and a range of key mill members. This role...