Clinical Trial Manager
4 semanas atrás
Clinical Trial Manager II you will play a key role in improving the lives of patients by accelerating the development of our customers drugs and devices through innovative solutions. What will you be doing? Primary point of contact to lead, manage and co-ordinate the conduct of clinical trials from study start-up (COLA) to close out at a country level in accordance with ICH-GCP and other applicable local regulations. Maintains the quality and scientific integrity of clinical trials at a country level. Collaborates with cross functional internal and external stakeholders to ensure timely execution, budget execution of clinical trial deliverables within the country. Maintains expert country, site and protocol knowledge to support sites with questions as well as build strong site relationships. Partners with global, local country teams and study team to provide high level country strategy, drive study progress and country level study delivery. Accountable for study deliverables and drives key decisions within set country. Acts as coordinating CTM to ensure consistency of training, processes and systems related practices as well as ad-hoc coordinating activities. Mentors junior level staff. What You Need to Have: Undergraduate degree or its international equivalent in clinical, science, or health related field from an accredited institution; a licensed healthcare professional (i.e. registered nurse); or equivalent work experience required. 7+ years of Clinical Research Experience required, including at least 2 years of experience in Clinical Trial Management. Knowledge of ICH and local regulatory authority applicable regulations. Read, write and speak fluent English; fluent in host country language required. Availability to go to the offices at least once a week - located in Buenos Aires, Argentina. What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: Various annual leave entitlements A range of health insurance offerings to suit you and your family’s needs Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others Visit our careers website to read more about the benefits of working at ICON: At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below: Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. #J-18808-Ljbffr
-
Clinical Project Manager **Level Dependent on Experience**
4 semanas atrás
São Paulo, Brasil CTI Clinical Trial and Consulting Services Tempo inteiroClinical Project Manager Level Dependent on Experience Join to apply for the Clinical Project Manager Level Dependent on Experience role at CTI Clinical Trial and Consulting Services Get AI-powered advice on this job and more exclusive features. CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research...
-
Clinical Trial Manager
Há 6 dias
São Paulo, São Paulo, Brasil ICON plc Tempo inteiro R$90.000 - R$120.000 por anoClinical Trial Manager (FSP - Sponsor Dedicated)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 developmentWe are currently seeking a Clinical Trial Manager to...
-
Clinical Trial Manager
3 semanas atrás
São Paulo, Brasil Syneos Health Tempo inteiroClinical Trial Manager Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of...
-
Clinical Trial Manager
4 semanas atrás
São Paulo, Brasil ICON Tempo inteiroClinical Trial Manager in IPH 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.
-
Clinical Trial Coordinator
3 semanas atrás
São Paulo, Brasil Merck Gruppe - MSD Sharp & Dohme Tempo inteiroJob Description Under the oversight of the line-manager, this role is responsible for comprehensive trial and site administration and involves preparing, collating, distributing and archiving clinical documents. The CTC supports clinical supply & non-clinical supply management and ensures timely maintenance of tracking and reporting tools, as applicable. The...
-
Clinical Project Assistant
1 semana atrás
Sao Paulo, Brasil CTI Clinical Trial Services, Inc Tempo inteiro**Clinical Project Assistant** **Job Purpose/Summary** Responsible for supporting management efforts of Clinical Project Managers and Directors, ensuring timelines, and quality standards are being achieved. **What You’ll Do** - Support Clinical Project Manager / Director in completing management activities; supports activities through all phases of a...
-
Clinical Trial Coordinator
3 semanas atrás
São Paulo, Brasil Merck Tempo inteiroJob Description Under the oversight of the line‑manager, this role is responsible for comprehensive trial and site administration and involves preparing, collating, distributing and archiving clinical documents. The CTC supports clinical supply & non‑clinical supply management and ensures timely maintenance of tracking and reporting tools, as applicable....
-
Clinical Trial Oversight Manager
Há 3 dias
São Paulo, Brasil Amgen Tempo inteiroCareer Category Clinical Job Description Join Amgen's Mission of Serving Patients At Amgen if you feel like you're part of something bigger it's because you are. Our shared mission to serve patients living with serious illnesses drives all that we do. Since 1980 we've helped pioneer the world of biotech in our fight against the world's toughest diseases....
-
Clinical Trial Manager
2 semanas atrás
Sao Paulo, Brasil ICON plc Tempo inteiroJob Advert Posting 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...
-
Clinical Trial Coordinator
3 semanas atrás
São Paulo, Brasil MSD Malaysia Tempo inteiroJob DescriptionUnder the oversight of the line-manager, this role is responsible for comprehensive trial and site administration and involves preparing, collating, distributing and archiving clinical documents. The CTC supports clinical supply & non-clinical supply management and ensures timely maintenance of tracking and reporting tools, as applicable.The...