Clinical Research Manager
4 semanas atrás
At ICON Plc, we're committed to fostering an inclusive environment that drives innovation and excellence. We're seeking a highly skilled Clinical Trial Manager II to join our team and contribute to the advancement of inNvative treatments and therapies.
Key Responsibilities:
- Collaborate with cross-functional teams to design and implement effective clinical trial enrollment strategies.
- Develop and implement comprehensive clinical trial protocols in collaboration with cross-functional teams.
- Oversee and manage the day-to-day operations of clinical trials, ensuring compliance with regulatory standards.
- Analyze and interpret clinical trial data, identifying trends and providing insights to optimize study outcomes.
- Proactively address challenges and implement effective solutions to ensure the successful execution of clinical trials.
- Communicate effectively with internal and external stakeholders to foster strong partnerships and facilitate smooth trial processes.
Requirements:
- Bachelor's degree
- Advanced English
- 3+ years clinical research experience, 1+ year experience as CRA
- Preferable CTM experience and early phase experience
- Proven expertise in designing and executing clinical trials, with a strong understanding of regulatory requirements
- Exceptional analytical and problem-solving skills, with the ability to interpret complex medical data
What ICON Offers:
- Competitive salary packages
- Annual bonuses reflecting delivery of performance goals
- A range of health-related benefits to employees and their families
- Competitive retirement plans and related benefits
- An inclusive and diverse work environment
ICON is an equal opportunity and inclusive employer, committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
-
Clinical Research Associate Lead
4 semanas atrás
São Paulo, São Paulo, Brasil Cti Clinical Trial Services, Inc Tempo inteiroJob SummaryClinical Trial Services, Inc. is seeking a highly skilled Clinical Research Associate Lead to join our team. As a Clinical Research Associate Lead, you will be responsible for overseeing the conduct of clinical trials at assigned sites, ensuring compliance with regulatory requirements, and providing guidance to site staff.Key...
-
Senior Clinical Research Manager
2 semanas atrás
São Paulo, São Paulo, Brasil CTI Clinical Trial Services, Inc Tempo inteiroClinical Research Excellence at CTI Clinical Trial Services, IncWe maintain a culture of excellence across all regions by ensuring our remote employees are fully engaged. To achieve this, we hold weekly all-staff meetings. Each department provides an update on their study or milestone progress. Additionally, our employees can participate in one of our CTI...
-
Clinical Research Manager
4 semanas atrás
São Paulo, São Paulo, Brasil Icon Plc Tempo inteiroAbout the Role:We are seeking a highly skilled Clinical Trial Manager II to join our team at ICON plc, a world-leading healthcare intelligence and clinical research organization. As a Clinical Trial Manager II, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of...
-
Regulatory Affairs Manager
4 semanas atrás
São Paulo, São Paulo, Brasil Intrials Clinical Research Tempo inteiroJob Title: Regulatory Affairs At Intrials Clinical Research, we are seeking a highly skilled and experienced Regulatory Affairs professional to join our team.Primary Responsibilities:Manage the Regulatory & Study Start-up team in all aspects, with support from the Regulatory and Study Start-up Manager (RSM).Support RSM in defining metrics and KPIs for the...
-
Regulatory Affairs Specialist
4 semanas atrás
São Paulo, São Paulo, Brasil Intrials Clinical Research Tempo inteiroJob Title: Regulatory Affairs SpecialistAbout the Role:We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Intrials Clinical Research. As a Regulatory Affairs Specialist, you will be responsible for managing regulatory and start-up activities for clinical trials in Latin America.Key Responsibilities:- Manage regulatory and...
-
Senior Clinical Research Associate
2 semanas atrás
São Paulo, São Paulo, Brasil CTI Clinical Trial Services, Inc Tempo inteiroPrincipal Clinical Research AssociateJob SummaryCTI Clinical Trial Services, Inc. is seeking a highly skilled and experienced Principal Clinical Research Associate to join our team. As a key member of our clinical operations team, you will be responsible for overseeing the management of clinical trials, ensuring compliance with regulatory requirements, and...
-
Clinical Research Associate
4 semanas atrás
São Paulo, São Paulo, Brasil Thermo Fisher Scientific Tempo inteiroClinical Research Associate Job DescriptionAt Thermo Fisher Scientific, we are seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will be responsible for ensuring the integrity and quality of clinical trials. Your primary focus will be on monitoring and managing clinical trials, ensuring compliance...
-
Clinical Trials Manager
4 semanas atrás
São Paulo, São Paulo, Brasil Medpace, Inc. Tempo inteiroKey Responsibilities:As a Regulatory Submissions Manager at Medpace, you will play a vital role in the clinical trial management process. Your primary focus will be on efficiently managing and successfully completing regulatory submissions for our LATAM clinical trials.Key Skills and Qualifications:• Strong expertise in clinical trial management and...
-
Clinical Research Associate
Há 1 mês
São Paulo, São Paulo, Brasil Novasyte Tempo inteiro**Job Overview**As a Clinical Research Associate, you will be responsible for ensuring the proper conduct of clinical trials at assigned sites. This includes performing site monitoring visits, administering protocol training, and evaluating the quality of study site practices.**Key Responsibilities:**Perform site monitoring visits to ensure compliance with...
-
São Paulo, São Paulo, Brasil Iqvia Tempo inteiroJob Title: Clinical Research CoordinatorWe are seeking a highly motivated and organized Clinical Research Coordinator to join our team at IQVIA in Curitiba, Brazil. As a Clinical Research Coordinator, you will be responsible for supporting the site team with various administrative tasks, including verifying research study information, researching queries,...
-
Clinical Operations Manager
4 semanas atrás
São Paulo, São Paulo, Brasil Msd Tempo inteiroThis role is accountable for performance and compliance for assigned protocols in a country in accordance with regulations, policies, quality standards, and adverse event reporting requirements.The person is responsible for budget/finance aspects, execution, and oversight of clinical trial country submissions and approvals, and ensuring Site...
-
Clinical Research Associate Lead
4 semanas atrás
São Paulo, São Paulo, Brasil PSI Tempo inteiroJob Title: Lead Clinical Research AssociateJob Summary:In this role, you will oversee local clinical research activities, ensuring the protection of trial subjects' rights, safety, and well-being, as well as data quality and study compliance on a country/regional level.Key Responsibilities:Facilitate regional projects as Lead Clinical Research Associate and...
-
Global Clinical Trials Manager
Há 7 dias
São Paulo, São Paulo, Brasil Allucent Tempo inteiroJob DescriptionWe are seeking an experienced Global Clinical Trials Manager to join our team at Allucent. As a key member of our clinical operations department, you will be responsible for providing leadership and management to the Clinical Research Associates (CRAs) and other clinical functional groups in their day-to-day clinical trial activities.Your...
-
Clinical Research Coordinator
Há 4 dias
São Paulo, São Paulo, Brasil SAO Fortrea Brazil Limitada Tempo inteiroSAO Fortrea Brazil Limitada Clinical Trials AssistantWe are seeking a highly motivated and organized Clinical Trials Assistant to join our team in Fortrea, Brazil.About the JobThe Clinical Trials Assistant will be an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. This role will involve performing...
-
Clinical Research Associate
4 semanas atrás
São Paulo, São Paulo, Brasil Icon Plc Tempo inteiroJob SummaryWe are seeking a highly skilled Clinical Research Associate to join our team at ICON Plc. As a Clinical Research Associate, you will be responsible for managing clinical trials and ensuring compliance with regulatory requirements.Key ResponsibilitiesManage clinical trials from initiation to close-outEnsure compliance with ICH GCP guidelines and...
-
Clinical Research Associate
4 semanas atrás
São Paulo, São Paulo, Brasil PSI CRO Tempo inteiroCompany OverviewPSI CRO is a leading Contract Research Organization with a strong presence in the industry, offering a perfect balance between stability and innovation to both clients and employees.Job ResponsibilitiesAs a Medical Monitor at PSI CRO, you will provide medical input to global clinical studies and advise the teams and business partners,...
-
Clinical Research Coordinator
1 semana atrás
São Paulo, São Paulo, Brasil Medpace, Inc. Tempo inteiroMedpace is a full-service clinical contract research organization (CRO) dedicated to accelerating the global development of safe and effective medical therapeutics. We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries.We are seeking a highly skilled Clinical Research Coordinator to support...
-
Clinical Research Associate
4 semanas atrás
São Paulo, São Paulo, Brasil Thermo Fisher Scientific Tempo inteiro**Clinical Operations Role**At Thermo Fisher Scientific, we're committed to enabling our customers to make the world healthier, cleaner, and safer. As a Clinical Research Associate, you'll play a crucial part in bringing our Mission to life by providing end-to-end support for clinical trials from study start-up to monitoring through to study close-out.**Key...
-
Clinical Research Associate
4 semanas atrás
São Paulo, São Paulo, Brasil Novasyte Tempo inteiro**Job Overview**As a Clinical Research Associate at Novasyte, you will be responsible for ensuring the quality and integrity of study site practices related to the proper conduct of clinical trials. This includes performing site monitoring visits, administering protocol and related study training, and evaluating the quality of study site practices.**Key...
-
Research Manager
4 semanas atrás
São Paulo, São Paulo, Brasil Mmr Research Tempo inteiroWe are seeking a highly skilled Research Manager to join our team at MMR, a global company specializing in food, drink, and consumer packaged goods research. As a Research Manager, you will be responsible for leading market research projects, involving client liaison and project management from research design through to final debrief presentations.Key...