Clinical Trial Coordinator
Encontrado em: Talent BR C2 - 1 semana atrás
Requirements:
Completed job training (finance), or Bachelor’s Degree 1-2 years of experience in Finance of clinical trials (focused on site payments); Advanced English Advanced Excel Hands-on Attention to detailsFortrea is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
-
Clinical Project Manager
Há 4 dias
Sao Paulo, Brasil CTI Clinical Trial Services, Inc Tempo inteiro**Clinical Project Manager** **(Level Depends on Experience)** **Job Purpose/Summary**: Responsible for management and oversight of assigned clinical trials (Phase I through Phase IV) to ensure client’s goals of time, budget and quality performance are met. The Clinical Project Manager I is expected to require support and guidance from Directors and/or...
-
Clinical Trial Assistant
Há 10 horas
Sao Paulo, Brasil IQVIA Tempo inteiroJob Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...
-
Clinical Trial Assistant
1 dia atrás
Sao Paulo, Brasil Novasyte Tempo inteiroJob Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...
-
Clinical Research Coordinator
Encontrado em: Talent BR C2 - 2 semanas atrás
São Luís, Brasil IQVIA Tempo inteiroAre you looking for an opportunity in Clinical Research?Do you want to work for an industry leading company that offers you experience and supports career progression whilst giving you the option of working flexibly? If so, come and join us - IQVIA are looking Clinical Research Coordinator. This role has an immediate start working 20 hours a week for a...
-
Clinical Trial Coordinator
Encontrado em: Talent BR C2 - 2 semanas atrás
São Paulo, Brasil Fortrea Tempo inteiroAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...
-
Clinical Trial Manager
Encontrado em: Talent BR C2 - Há 5 dias
São Paulo, Brasil IQVIA Tempo inteiroClinical Trial Manager The Clinical Trial Manager provides leadership of the clinical team, in support of the project leader, and in collaboration with the other functional teams, to achieve the delivery of the project’s overall objectives to the Sponsor’s satisfaction per contract while optimizing speed, quality and cost of delivery and in...
-
Clinical Trial Management Associate Manager
Encontrado em: Talent BR C2 - 2 semanas atrás
São Paulo, Brasil BeiGene Tempo inteiroBeiGene continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer. PLEASE SUBMIT ALL RESUMES/CV'S IN ENGLISH FOR...
-
Clinical Trial Administrator II
Encontrado em: Talent BR C2 - Há 7 dias
São Paulo, Brasil PSI CRO Tempo inteiroJob DescriptionJoin our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & information. Only CVs in English will be accepted.You will be responsible for:Customization of Site ICF/patient documents before sending it to sites;EC- IRB submissions;Site Room, Veeva...
-
Clinical Trial Administrator II.
Encontrado em: Talent BR C2 - Há 7 dias
São Paulo, Brasil PSI Tempo inteiroJob Description Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & information. Only CVs in English will be accepted. You will be responsible for: Customization of Site ICF/patient documents before sending it to sites; EC- IRB submissions; ...
-
Clinical Trial Coordinator
Encontrado em: Talent BR C2 - 1 semana atrás
São Paulo, Brasil Fortrea Tempo inteiroAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...
-
Clinical Operations Manager
Encontrado em: Talent BR C2 - 2 semanas atrás
São Paulo, Brasil Fortrea Tempo inteiroAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...
-
Clinical Scientist
Encontrado em: Talent BR C2 - 2 semanas atrás
São Paulo, Brasil IQVIA Tempo inteiroPURPOSE The Clinical Scientist supports medical monitoring and scientific tasks on projects under the guidance of Therapeutic Medical Advisors (TMA) and in collaboration with the cross functional project team. These activities enable the use of high quality, scientific data to make timely decisions during clinical study planning, execution, analysis, and...
-
Clinical Trial Coord
Há 6 dias
Sao Paulo, Brasil Thermo Fisher Scientific Tempo inteiroAccording to the specific role (Central or Local), coordinates, oversees and completes functions on assigned trial(s) activities as detailed on the task matrix. Performs department, Internal, Country and Investigator file reviews as assigned, and documents findings in appropriate system(s). Ensures allocated tasks are performed on time, within budget and...
-
Clinical Team Lead
Encontrado em: Talent BR C2 - 1 semana atrás
São Paulo, Brasil Fortrea Tempo inteiroAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...
-
Clin Trials Assistant
Encontrado em: Talent BR C2 - 1 semana atrás
São Paulo, Brasil Fortrea Tempo inteiroAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...
-
CMM - Clinical Medical Manager (Talent Pipeline)
Encontrado em: Talent BR C2 - 1 semana atrás
São Paulo, Brasil Novo Nordisk AS Tempo inteiroStep into the Future: Join Novo Nordisk's Talent Pipeline! Are you ready to shape the future of healthcare with Novo Nordisk? We are thrilled to announce an opportunity within our Talent Pipeline, where we actively seek top-tier professionals to join our pioneering team in the first semester of 2024. The Talent Pipeline provides an exceptional...
-
Senior Specialist
Encontrado em: Talent BR C2 - 1 semana atrás
São Paulo, Brasil Fortrea Tempo inteiroThe Clinical & Ancillary Supplies Services (CASS) Senior Specialist: Coordinate and oversee aspects of logistics related to Clinical and Ancillary Supplies services. Support these services to both internal and external clients. Responsible for the set-up and coordination of project activities related to clinical and ancillary supplies Independently...
-
Senior Specialist
Encontrado em: Whatjobs BR C2 - 1 semana atrás
São Paulo, Brasil Fortrea Tempo inteiroThe Clinical & Ancillary Supplies Services (CASS) Senior Specialist: Coordinate and oversee aspects of logistics related to Clinical and Ancillary Supplies services. Support these services to both internal and external clients. Responsible for the set-up and coordination of project activities related to clinical and ancillary supplies Independently...
-
Director, Clinical Development Oncology – LATAM region
Encontrado em: Talent BR C2 - 1 semana atrás
São Paulo, Brasil Gilead Sciences Farmaceutica do Brasil Ltda Tempo inteiroDescription For over 30 years, Gilead has been a leading innovator in the field of virology, having developed many of today’s leading medicines for treating and preventing HIV and viral hepatitis. More recently, Gilead has expanded its oncology portfolio, and seeks to become a leader in this critical disease area. In this role as Director,...
-
Trial Capabilities Associate
Encontrado em: Talent BR C2 - 2 semanas atrás
São Paulo, Brasil Lilly Tempo inteiroWe’re looking for people who are determined to make life better for people around the world. Principais desafios: Initiate investigator activities, including collection and submission of regulatory documents, customization and negotiation of informed consent documents, serve as the point of contact for an investigator’s ERB and Competent Authority...