Clinical Trial Manager
Há 3 dias
Job Opportunity Overview Our organization is seeking a highly skilled professional to play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. Compliance with all ICH-GCP guidelines, regulations, SOPs, and study processes will be ensured by completing onsite and remote monitoring activities. Proper informed consent procedures and protocol adherence to applicable regulations will be verified to protect study participants. The integrity of clinical data will be maintained, and the study will be conducted in compliance with approved protocols, GCP, regulations, and SOPs, ensuring accurate results. Effective management of investigative site staff will be facilitated to deliver trial objectives, such as subject enrollment and data submissions. Investigational Product (IP) management and accountability will be verified to ensure proper handling and control. Site-specific findings and updates will be documented in reports, which will also include relevant tracking system inputs. Key Responsibilities Design and analyze clinical trials to advance innovative treatments and therapies. Interpret complex medical data to inform decision-making. Contribute to the development of new treatment options and therapies. Collaborate with cross-functional teams to achieve project goals. Stay up-to-date with industry developments and best practices. Requirements Strong understanding of ICH-GCP guidelines and regulatory requirements. Excellent analytical and problem-solving skills. Ability to work effectively in a team environment. Strong communication and interpersonal skills. Proficiency in relevant software applications. What We Offer Our organization provides a dynamic and challenging work environment that fosters growth and development. We offer competitive compensation packages and opportunities for career advancement. A successful candidate will have the opportunity to make a meaningful contribution to the advancement of healthcare and contribute to the success of our organization.
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Clinical Trial Manager
Há 3 dias
Salvador, Brasil Bebeeclinicaltrialmanager Tempo inteiroJob Opportunity OverviewOur organization is seeking a highly skilled professional to play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.Compliance with all ICH-GCP guidelines, regulations, SOPs, and study processes will be ensured by...
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Clinical Project Professional
1 dia atrás
Salvador, Brasil beBeeProject Tempo inteiroClinical Project Manager Role Clinical project managers play a pivotal role in the success of clinical projects, ensuring regulatory compliance and effective budget forecasting.
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Clinical Site Manager
2 semanas atrás
Salvador, Brasil Nutricio Tempo inteiroClinical Site Manager – (Ophthalmology & Neurology Focus) Location: Remote-based We’re partnering with a global biopharmaceutical company dedicated to advancing treatments in Ophthalmology, Neurology , and other complex therapeutic areas. To support several ongoing and upcoming studies, we are seeking a Clinical Site Manager to oversee key investigator...
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Freelance Clinical Research Associate
4 semanas atrás
Salvador, Brasil IQVIA Tempo inteiroJoin IQVIA Biotech as a Freelance CRA supporting Phase 2 and 3 clinical trials. You’ll lead site visits, monitor compliance, and ensure high-quality data—all while working with a passionate team.We currently have two projects in Brazil:Location: Brazil - travel required for both roles across BrazilHours: 1 x 0.35 FTE and 1 x 0.6 FTEStart: ASAPDuration: 6...
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Clinical Project Professional
Há 24 horas
Salvador, Brasil Bebeeproject Tempo inteiroClinical Project Manager RoleClinical project managers play a pivotal role in the success of clinical projects, ensuring regulatory compliance and effective budget forecasting.
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Freelance Clinical Research Professional
Há 5 horas
Salvador, Brasil Bebeeresearch Tempo inteiroAbout the RoleWe are seeking a skilled Freelance Clinical Research Associate (CRA) to support Phase 2 and 3 clinical trials.Key Responsibilities:Conduct site evaluations, initiations, monitoring & close-outsEvaluate compliance and ensure data integrityCollaborate with investigators and internal teamsReview protocols and study manualsSupport site staff with...
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Sr. Clinical Operations Lead
1 dia atrás
Salvador, Brasil Alimentiv Tempo inteiroResponsible for the clinical operations of a project at the regional/global level. The Clinical Operations Lead oversees project deliverables, Clinical Research Associates (CRAs), and investigator sites in accordance with monitoring plans, protocols, Good Clinical Practice (GCP), ICH guidelines, and local regulations. The role serves as the primary liaison...
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Sr. Clinical Operations Lead
Há 23 horas
Salvador, Brasil Alimentiv Tempo inteiroResponsible for the clinical operations of a project at the regional/global level. The Clinical Operations Lead oversees project deliverables, Clinical Research Associates (CRAs), and investigator sites in accordance with monitoring plans, protocols, Good Clinical Practice (GCP), ICH guidelines, and local regulations. The role serves as the primary liaison...
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Sr. Clinical Operations Lead
2 semanas atrás
Salvador, Brasil Alimentiv Inc. Tempo inteiroResponsible for the clinical operations of a project within a defined regional/global level.Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and Investigator sites in accordance with the Monitoring Plan, Protocol, Good Clinical Practice (GCP), ICH guidelines and local regulations.The COL acts as a primary liaison...
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Sr. Clinical Operations Lead
2 semanas atrás
Salvador, Brasil Alimentiv Inc. Tempo inteiroResponsible for the clinical operations of a project within a defined regional/global level. Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and Investigator sites in accordance with the Monitoring Plan, Protocol, Good Clinical Practice (GCP), ICH guidelines and local regulations. The COL acts as a primary liaison...
