Data Manager for Clinical Trials
4 semanas atrás
Job Description Clinical Data Manager plays a critical role in the clinical research project. If you are detail-oriented and committed to quality, able to work with large volume of clinical or medical data, you might be the professional we are looking for. Please submit your CV in English Based in Brazil Responsibilities will include: Track database set-up, testing, maintenance and data entry Communicate with clients, project teams and vendors on data management matters Review study documents, design and develop project specific guidelines and instructions Design eCRF, Data Management and Data Validation Plans and test EDC databases Ensure data entry, follow-up and validation, including manual CRF review and SAE reconciliation Code medical data Track and report metrics leading to database lock Coordinate the processing, dispatch and archiving of CRFs/queries Maintain Clinical Data Management working files Perform database QC checks, prepare and attend audits Train site staff and project teams on CRF completion and data management topics Qualifications College/University degree (Life Science, Pharmacy degree is a plus) Demonstrated experience of managing clinical or medical data Full working proficiency in English Experience with Clinical Data Management systems (e.g. Medidata Rave, Oracle InForm) Proficiency in MS Office applications Organisational and time management skills Ability to work independently and multi-task Additional Information If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you. #J-18808-Ljbffr
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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...
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Data Manager for Clinical Trials
2 semanas atrás
São Paulo, State of São Paulo, Brazil PSI CRO Tempo inteiro R$30.000 - R$60.000 por anoCompany Description PSI is a leading Contract Research Organization (CRO) with over 25 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects...
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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...
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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...
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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...
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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....
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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.
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Clinical Trial Manager II
1 semana atrás
São Paulo, Brasil Syneos Health Tempo inteiroJoin to apply for the Clinical Trial Manager II role at Syneos Health . 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...
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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...
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Clinical Trial Coordinator
3 semanas atrás
São Paulo, Brasil MSD Brasil 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....