Clinical Trials Specialist
2 semanas atrás
Job Title: Medical Science Liaison Job Description: As a Medical Science Liaison, you will serve as a key scientific resource for stakeholders, facilitating clinical trial activities and generating insights to inform strategy and improve patient outcomes. Clinical Trial Support: Collaborate with clinical trial teams to support trial enrollment efforts, including identifying suitable patients and optimizing recruitment strategies. Engage with clinical trial sites and investigators to ensure smooth trial operations and alignment with study objectives. Provide education and training to clinical sites on study protocols and therapeutic areas. Insight Generation and Framework Creation: Gather and synthesize insights from healthcare professionals (HCPs), patients, and other stakeholders to identify referral patterns, challenges, and opportunities for trial enrollment. Develop frameworks to streamline patient identification and referral pathways. Stakeholder Engagement: Build and maintain relationships with HCPs, clinical trial investigators, and other key opinion leaders (KOLs) in dermatology. Act as liaison between clinical sites, investigators, and internal teams to ensure effective communication and support. Cross-Border Collaboration: Work across national borders to address global clinical trial needs and ensure compliance with international regulations and cultural nuances. Collaborate with global teams to align on strategies and share best practices. Qualifications and Experience: Minimum 3 years of experience as Medical Science Liaison or similar role. Strong background in dermatology or rheumatology, with experience engaging with dermatologist-focused clinical trial sites and investigators. Proven track record of supporting clinical trial enrollment, patient identification, and site engagement. Experience generating insights and developing frameworks to address complex challenges in clinical trial operations. Demonstrated ability to identify patient referral patterns and address barriers to patient participation. Willingness to travel extensively, including international travel. Experience working in cross-border settings and collaborating with global teams. Exceptional interpersonal and communication skills, with ability to build relationships with diverse stakeholders. Strong organizational and time-management skills, with ability to work independently.
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Lead Clinical Trial Programmer
2 semanas atrás
Curitiba, PR, Brasil beBeeClinical Tempo inteiroSenior Clinical Data Science Programmer Job Description As a Senior Clinical Data Science Programmer, you will play a pivotal role in developing and implementing programming solutions to support the analysis and reporting of clinical trial data. Develop and maintain programming solutions for CDMS (EDC systems), data validation outputs, data review/risk...
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Clinical Trial Manager
2 semanas atrás
Curitiba, Brasil NonStop Consulting Tempo inteiroWould you like to build your career within one of the 10 top CROs in a world?Our client is looking for Clinical Trial manager to join their teams in Argentina and Brazil, giving you flexibility and an opportunity to progress your career!**Requirements**:Completed degree in a health-related field;Experience in Phases 1-4 (Phases 2-3 preferred)3+ years as a...
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Research Associate Specialist
2 semanas atrás
Curitiba, PR, Brasil beBeeClinical Tempo inteiroJob Title: Research Associate Specialist Job Summary: We are seeking a detail-oriented and experienced Clinical Research Associate (CRA) to monitor and manage Phase 2 clinical trials. The CRA will ensure the trial is conducted in compliance with regulatory standards, Good Clinical Practice (GCP), and the study protocol. Key Responsibilities: Ensure site...
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Lead Clinical Trial Programmer
3 semanas atrás
Curitiba, Brasil beBeeClinical Tempo inteiroSenior Clinical Data Science Programmer Job Description As a Senior Clinical Data Science Programmer, you will play a pivotal role in developing and implementing programming solutions to support the analysis and reporting of clinical trial data. Develop and maintain programming solutions for CDMS (EDC systems), data validation outputs, data review/risk...
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Clinical Trial Manager
1 semana atrás
Curitiba, Brasil Nonstop Consulting Tempo inteiroWould you like to build your career within one of the 10 top CROs in a world?Our client is looking for Clinical Trial manager to join their teams in Argentina and Brazil, giving you flexibility and an opportunity to progress your career!Sites are in Buenos Aires and Sao Paolo.There is also an option to work fully remote, for those who have 5+ years of...
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Clinical Trial Manager
4 semanas atrás
Curitiba, Brasil NonStop Consulting Tempo inteiroOur client, a growing and developing global CRO, offering a great opportunity and career progression, is hiring a Clinical Trial Manager.Our client is based around the globe and are in search of someone based in Brazil, with a great list of benefits, which include:- Career progression- Open communication- Work in a top rated CRO- Stable environment- To work...
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Clinical Data Lead
3 semanas atrás
Curitiba, PR, Brasil beBeeClinicalData Tempo inteiroLead Clinical Data Programmer Role About the Job: We are seeking a highly skilled Clinical Data Programmer to join our team. The successful candidate will be responsible for developing, validating, and maintaining programming solutions for clinical trials. The ideal candidate will have extensive experience in programming for CDMS (EDC systems such as...
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Clinical Trial Manager
Há 6 dias
Curitiba, Brasil NonStop Consulting Tempo inteiroClinical Trial ManagerMy Client who is a full-service clinical CRO is currently looking for a Clinical Trial Manager (PM) to join their team in Buenos Aires, Argentina or San Paolo, Brazil. They provide Phase I to IV clinical development services to biotechnology, pharmaceutical and medical devices companies. They offer an industry recognised 2 month...
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Clinical Trial Manager
Há 7 dias
Curitiba, Brasil NonStop Consulting Tempo inteiroClinical Trial Manager My Client who is a full-service clinical CRO is currently looking for a Clinical Trial Manager (PM) to join their team in Buenos Aires, Argentina or San Paolo, Brazil. They provide Phase I to IV clinical development services to biotechnology, pharmaceutical and medical devices companies. They offer an industry recognised 2 month...
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Clinical Data Lead
3 semanas atrás
Curitiba, Brasil beBeeClinicalData Tempo inteiroLead Clinical Data Programmer Role About the Job: We are seeking a highly skilled Clinical Data Programmer to join our team. The successful candidate will be responsible for developing, validating, and maintaining programming solutions for clinical trials. The ideal candidate will have extensive experience in programming for CDMS (EDC systems such as...
